| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs28545275 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901968 | AAGGAGCTCATTACA[C/G]AAAAACGGTGAAGGG | 5336 |
| rs28545282 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874667 | TTATAATCCCCAGAA[C/G]TAAATCCAGGGAGTG | 5336 |
| rs28546769 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824324 | TTTTTAGTAGAGACA[A/G]GGTTTCACCACGTTG | 5336 |
| rs28550771 | snp | A/C | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824444 | TGGCCCCAGCCACTT[A/C]TTTTCTTGTGATTTG | 5336 |
| rs28580080 | snp | C/T | 0.135484 | 0.22223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861653 | GGTCTCTTTCAGCCT[C/T]GGAGGTGATGCCTCT | 5336 |
| rs28603034 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869950 | CTGCATCCAAACAGC[C/T]CCAGTTGGAGGACTC | 5336 |
| rs28605963 | snp | C/G | 0.45645 | 0.140991 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851929 | ACTTAATTGTCTGCT[C/G]TCCTCCTCTAGCTCC | 5336 |
| rs28609062 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824658 | CGGTTATAATTAAAG[A/G]GCAACACTGAGGCCA | 5336 |
| rs28613794 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866280 | ACCAGCATGAGAGGA[C/T]GCTAGCCTCTCCCTT | 5336 |
| rs28613941 | snp | A/G | 0.1652 | 0.235179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859590 | CCCAGGCTGGAGTGC[A/G]GTGGCATGATCTCAG | 5336 |
| rs28639608 | snp | G/T | 0.402806 | 0.197864 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796843 | TGGTCTCCAGAACTG[G/T]GAGACAAACTTCTGT | 5336 |
| rs28660558 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866337 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs28668056 | snp | A/G | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856453 | CAATGCCGCTTATTA[A/G]CAAGGGTAATAGCAA | 5336 |
| rs28690049 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874614 | GGCCTAGCTGGATTT[C/G]TCAGGCTCCTGCAGG | 5336 |
| rs28699461 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868493 | TGATTCTGCCAAGCC[C/T]GTCCTGTGGTTTTGG | 5336 |
| rs28716785 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866284 | GCATGAGAGGATGCT[A/G]GCCTCTCCCTTTCTC | 5336 |
| rs28731296 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824700 | ATCCTCTCGTAGCTG[C/T]CATGTGACCTCTGGC | 5336 |
| rs28734133 | snp | A/G | 0.306182 | 0.243605 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840430 | GTGTACTTCATTTAT[A/G]TTATGATTACATTGT | 5336 |
| rs28880295 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917349 | ATGGTGAATGGTGCT[A/G]TGAACATGGGAGTGC | 5336 |
| rs33998770 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782112 | GATCTCCTGACCTCA[-/A]TGATCCGCCCACCTC | 5336 |
| rs34004978 | in-del | -/A/AA/AAA | 0.473266 | 0.112482 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930747 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GCCATTTAAATTATT | 5336 |
| rs34013291 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955429 | ACAGAGTAGTCAGGG[-/G]ATCCTCTGAAACAGA | 5336 |
| rs34017079 | in-del | -/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810656 | CTTTTTTTTTTTTTT[-/T]GCTGGTGATGTTGCT | 5336 |
| rs34024958 | in-del | -/A | 0.41408 | 0.188621 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858118 | GGCCATGACGGTGTG[-/A]AAGGGGATGCTTTCT | 5336 |
| rs34028338 | snp | C/G | 0.140919 | 0.224948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854372 | GGCTGTGCCTGGGCT[C/G]CAGTTGTGTGGCTGC | 5336 |
| rs34043434 | in-del | -/TC | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871858 | CCATCTGAATGTCTC[-/TC]AATGGAGGAATTGCT | 5336 |
| rs34044546 | in-del | -/T | 0.453473 | 0.145254 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783833 | TAACTCTCAGCAGGG[-/T]TTTTTTTTAGCATAC | 5336 |
| rs34048665 | in-del | -/T | 0.430136 | 0.173352 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881810 | CATGTCCAGCTATTG[-/T]TTTTTTTTTTTTTGT | 5336 |
| rs34053800 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81897192 | GCCGACTCCTGGTTT[-/T]GGGTTCCTTGTTATT | 5336 |
| rs34065286 | in-del | -/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881246 | ATAGTTTTTTTTTTT[-/T]AATTACAAAAACTAA | 5336 |
| rs34085404 | multinucleotide-polymorphism | AA/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857031 | GATCTCATGCAACCA[AA/GT]CTATTTTAGACTTCT | 5336 |
| rs34107670 | snp | C/T | 0.339429 | 0.233457 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855995 | ACCCCCTGTTCTTAA[C/T]TTGGTAAGGAGACCA | 5336 |
| rs34128992 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887117 | TTGGCCAGGCAAAGT[G/T]GTTTTTTTTTTTTTT | 5336 |
| rs34130863 | in-del | -/AA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849796 | AAAAAAAAAAAAAAA[-/AA]CCAAAAAAATTCCCT | 5336 |
| rs34132654 | in-del | -/G | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803135 | TTTTTTTTTTTTTTT[-/G]TGAGACGGAATCTCA | 5336 |
| rs34133634 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843558 | GCCTACCAATATTTT[-/T]CGCGTGAATACAAAG | 5336 |
| rs34142641 | snp | C/G | 0.424037 | 0.179474 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929316 | GCAGGCACGGGCATG[C/G]TCCCCTAGGACTCAG | 5336 |
| rs34154117 | in-del | -/A | 0.34526 | 0.23114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935427 | CTTTGGGGGCCATTT[-/A]AAAAAAAAAAGACCT | 5336 |
| rs34163417 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866271 | CACTGGGGCACCAGC[A/G]TGAGAGGACGCTGGC | 5336 |
| rs34183431 | in-del | -/T | 0.499312 | 0.0185358 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897549 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCCC | 5336 |
| rs34195031 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866308 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs34214092 | snp | C/G | 0.298398 | 0.245271 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915039 | ACTTTTTCAAACCCT[C/G]TCTGGTCAGGGTATG | 5336 |
| rs34217305 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849955 | ACCTTAATACCTTTC[-/C]AAGTTTTTAGATAAT | 5336 |
| rs34233969 | snp | A/G | 0.141934 | 0.225437 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792413 | TTGAATGTGCAAGGC[A/G]GAGGCTGCAGTGAGC | 5336 |
| rs34240208 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920808 | GGTGTAAATACTTCC[-/C]ATGGAGGTCAGTTTC | 5336 |
| rs34253259 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836189 | AGAGACTATCCAAAT[A/G]ACACAGCTGACCCAA | 5336 |
| rs34261675 | in-del | -/C | 0.437683 | 0.165152 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807211 | CTCCCCATGTCTTGT[-/C]CCAGCGGTGTCCTCC | 5336 |
| rs34271990 | in-del | -/A/T | 0.152334 | 0.230133 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885634 | AGAACTTTTTTTTTT[-/A/T]AAAATATAGCCATAA | 5336 |
| rs34277637 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815250 | AGTGAAGGGAGGGGG[-/G]TTCCCAGCTCTCCCT | 5336 |
| rs34310994 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81817715 | GTCTAAAACTCCCAG[-/T]ACTCAAGCGACCCCC | 5336 |
| rs34314759 | snp | C/G | 0.100588 | 0.200439 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862744 | GGGTGTAGTGGTGCA[C/G]ATTTGTAGTCCTGCT | 5336 |
| rs34324132 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882203 | CAGAATGTACTCCCC[-/C]ATCCAACCCGGGGGT | 5336 |
| rs34332984 | snp | A/G | 0.398534 | 0.201091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795263 | GTACTGTAATAAGGA[A/G]TCATTAGTCAGGAGC | 5336 |
| rs34340682 | in-del | -/T | 0.384209 | 0.210922 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787210 | ACTATCATTGTACTC[-/T]TTTTTTTTTAAAACA | 5336 |
| rs34364352 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868008 | GCCTGGCCCTCGCTT[-/A]CCCGCTTCAGCTGAA | 5336 |
| rs34385270 | in-del | -/T/TT | 0.404209 | 0.196773 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833535 | ATCTTTTTTTTTTTT[-/T/TT]GAGTCAGGATTTCAC | 5336 |
| rs34387550 | in-del | -/T | 0.342134 | 0.232404 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868314 | CCCACTTCCCCTCCC[-/T]GGCCCTTAGTGACCT | 5336 |
| rs34401463 | in-del | -/G | | | frameshift-variant | PLCG2 | GRCh38.p7 | 16:81937899 | GATGACGCTGACAGT[-/G]CAAGGTAAAGCCAGC | 5336 |
| rs34402931 | snp | A/G | 0.181659 | 0.240478 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854023 | GGAAAAGGTCATCAA[A/G]GTCAAGGTCAACCGG | 5336 |
| rs34431511 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832375 | TCTTCTTTTCCTTTT[-/T]GAGTAGAATCTGTCC | 5336 |
| rs34451275 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842838 | GAGACGTACGGAGGG[-/C]GCCAAAAGTCCGCAA | 5336 |
| rs34456557 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917091 | AACCACCATTCTACT[C/G/T]TCCACTTCCGTGAGT | 5336 |
| rs34457613 | snp | A/G | 0.498503 | 0.0273153 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948686 | GATTTCCTTACACCT[A/G]GGGAGACCTGGAGGG | 5336 |
| rs34471641 | in-del | -/AAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835597 | TATAATAATAATAAT[-/AAT]CATAATAATAATGAT | 5336 |
| rs34497020 | in-del | -/GT/TG | 0.400134 | 0.199899 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884602 | TGTGTGTGTGTGTGT[-/GT/TG]ACATGTATGCATGTC | 5336 |
| rs34508776 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815311 | AGTCCTCACCAAGGG[-/G]TCTCAGCCTCAGCAG | 5336 |
| rs34517941 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81895643 | TGTAAGCGCACAGGG[-/G]AACCCTGCGGATACA | 5336 |
| rs34536055 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81880009 | CTGAGGGGGCTCAGG[-/C]AGGGAGCATCTCTTG | 5336 |
| rs34567400 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935840 | TTCTCTTACCCAAAA[-/C]CCATTCCCATTCTCC | 5336 |
| rs34595643 | in-del | -/T | 0.41507 | 0.187755 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885331 | CCCAGCCCCGACTAA[-/T]TTTTGTATCTTTAGT | 5336 |
| rs34603417 | snp | A/G | 0.394171 | 0.204242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807104 | TCAAGTCTGTTCAAT[A/G]CATTTCCTTCTCCAG | 5336 |
| rs34608181 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894846 | CCGCTGCACGCCAGC[-/C]TGGGCAACAGAGGGA | 5336 |
| rs34611730 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893559 | TGTATTTCTGTCCTA[A/G]GCCTTAGCTTTGAGT | 5336 |
| rs34613969 | in-del | -/C | 0.140919 | 0.224948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934999 | TGGGAGCTACAATTC[-/C]AAGGTGAGATTTGGG | 5336 |
| rs34625255 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911064 | TGAAAATGAACAAGG[-/G]AAACAATGATTATAA | 5336 |
| rs34639082 | snp | G/T | 0.213635 | 0.247341 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929600 | AGGGTTTCGCCATGT[G/T]GGCCAGGCTGGTCTC | 5336 |
| rs34640368 | snp | A/G | 0.47934 | 0.0995154 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899607 | ACAAGTGTCCTCACC[A/G]TCTGTTGACTGCCAT | 5336 |
| rs34652684 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920789 | AGCATTTGCCAGTTT[-/C]CCATGGTGTAAATAC | 5336 |
| rs34681982 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800143 | GTATCATACTTTGGG[-/G]TATCATAGTACCTGG | 5336 |
| rs34688795 | in-del | -/C | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962835 | TATCCTATTTATCCC[-/C]ACGTTTCTTTGGGTT | 5336 |
| rs34698199 | in-del | -/T | 0.457271 | 0.139781 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787536 | CCCAGCCTTGCACTC[-/T]TTTTTTTTTTTTTTA | 5336 |
| rs34704719 | snp | C/T | 0.394904 | 0.203722 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794411 | TCCATTGTCTGAGGG[C/T]GGTCCCCAAGCCCCT | 5336 |
| rs34723428 | in-del | -/TT | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823693 | ATTTTTTTTTTTTTT[-/TT]CCCTGTAGAGACAGG | 5336 |
| rs34738788 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856687 | CAGTGGTACTCATCC[-/C]ATGGGAAGCTGAATA | 5336 |
| rs34748139 | snp | C/T | 0.212425 | 0.24716 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852349 | ATTCCCTGGCCCCTG[C/T]TGTCGCCTTCAGCTT | 5336 |
| rs34761601 | in-del | -/G | 0.483109 | 0.0903335 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870829 | CATCAAAAATCATGT[-/G]GTCACTTTTTTCATA | 5336 |
| rs34765849 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953125 | TACAAAATAACTGAC[-/C]TAGTATTCTTCCAAA | 5336 |
| rs34782773 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924595 | CTTACACTCTTAACT[C/T]CATTCATCTGCTAAG | 5336 |
| rs34823904 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81895386 | AACATGGTGCAACCC[-/C]TGTCTCTACTAAAAT | 5336 |
| rs34826185 | snp | A/G | 0.151668 | 0.229849 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832105 | TCCTTTGATAAATGG[A/G]GGGGGGGAATAGTGA | 5336 |
| rs34836329 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850230 | ATTATCATCAGTTTT[-/T]GTTAGGTGTAAGGTT | 5336 |
| rs34850739 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785883 | CTGAAGTTCATGCCC[-/C]TGTTAACTAAACCCC | 5336 |
| rs34873721 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81831738 | GTAATGGGGACCCCA[-/A]GGAGGCTCCCCGCTC | 5336 |
| rs34876455 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952972 | TTACCAACCACCTGG[-/G]AATAAGGCAGGTTGA | 5336 |
| rs34888880 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789433 | AGCTGAGACTACAGG[-/G]TGAGTGCCACCATGC | 5336 |
| rs34889398 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933676 | GTGTGGATTGACTTA[A/G]GTAATATCCCTCAAG | 5336 |
| rs34933363 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875225 | GCCTTGGCCTCCCAA[-/A]GGTGCTGGGATTACA | 5336 |
| rs34933932 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861400 | TTGGGTGAGCTTCCC[-/C]TGGTTTCTTCACATG | 5336 |
| rs34941159 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848765 | CAGTGGTGAAGAAGG[-/G]TGTACAATCCCTGCG | 5336 |
| rs34951925 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81819491 | CCTCCTGGCTCCTCG[-/G]CCCACTGCTTTTCAC | 5336 |
| rs34961611 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866227 | GCATGAGAGGACGCT[A/G]GCCTCTCCCTTTCTC | 5336 |
| rs35004238 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906369 | TTTGAGTATATTTTT[-/T]ACATGTCCGTTCTTA | 5336 |
| rs35014411 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805798 | TTTTTTTTTTTTTTT[-/T]GCTGTTATTGTTGTT | 5336 |
| rs35027472 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911815 | TTTTTTTTTTTTTTT[-/T]GGGACAGAGTCACAT | 5336 |
| rs35028362 | in-del | -/TAGA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940722 | CACAGCTGAGATAGA[-/TAGA]CACTTCCAGGTGAGG | 5336 |
| rs35028755 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810010 | TTTTTTTCTTTTTTT[-/T]GAGATGGAGCCTACC | 5336 |
| rs35033377 | in-del | -/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799616 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 5336 |
| rs35039495 | snp | A/C | 0.499776 | 0.0105807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870770 | ATGCCATTTCTGAAA[A/C]AAAAATTATTCTATA | 5336 |
| rs35058756 | in-del | -/A/AA | 0.34146 | 0.23267 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855192 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 5336 |
| rs35091405 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866627 | ATGAGAGGATGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs35123518 | in-del | -/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959951 | CCCAAATGGGTTTTT[-/T]GCTACCATATCAAAG | 5336 |
| rs35142664 | snp | G/T | 0.442249 | 0.159814 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803364 | TTAGCCTAACATAAG[G/T]TTCGTTCATATTGTA | 5336 |
| rs35152444 | snp | A/G | 0.105924 | 0.204309 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959865 | TCAGGTGTTGCTGTC[A/G]TTACCTCCTTTCAGC | 5336 |
| rs35154942 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848511 | TGTGCGTTTGCATTT[A/C]TCTCCCTCCTTGTCT | 5336 |
| rs35197248 | snp | C/T | 0.114387 | 0.210022 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960024 | CTCCAGCTGCTGCTG[C/T]GTAAAATCCATGCGT | 5336 |
| rs35205556 | snp | C/T | 0.388964 | 0.20782 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903918 | ATGAGGTGGAAATAG[C/T]GTTGGCCACACGGTC | 5336 |
| rs35211335 | snp | A/G | 0.114738 | 0.210248 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862686 | ACCAGCTTGGGCAAC[A/G]TGGGGAAACCCTGTC | 5336 |
| rs35214525 | in-del | -/G | 0.491629 | 0.0641526 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926089 | GAGTCTTAAATTAGT[-/G]GGGGGGAAGTTGGGT | 5336 |
| rs35232485 | in-del | -/TTTT | 0.306679 | 0.24349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785497 | TTTTCGTTTATTTCA[-/TTTT]TTTTTTTTTTTTGTT | 5336 |
| rs35255220 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906282 | TCCTCCAACTGGGGG[-/G]TCGTTCCACCAGAAA | 5336 |
| rs35283641 | snp | C/T | 0.354665 | 0.227036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877270 | CCATCCTGGCTGACA[C/T]GGTGAAACCCTGTCT | 5336 |
| rs35287968 | in-del | -/T | 0.316243 | 0.241064 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816483 | TAATTTTTTTTTTTT[-/T]GAGACACGGTCTCAT | 5336 |
| rs35288622 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941578 | ATTTTTTTTTTTTTT[-/T]GTACTCTAGAAATGT | 5336 |
| rs35319567 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787127 | ATGGCGCAGGCCTCA[A/G]TGTAACAGTTTAACT | 5336 |
| rs35320465 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820306 | TCCCTCTGCAGTCTG[-/G]CAGCCCCCCACCCTC | 5336 |
| rs35326209 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803030 | TACTTTCCCCCATCC[-/C]TGGCAATGACAAATC | 5336 |
| rs35351401 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864733 | GGAGGTGCCGGCCCA[G/T]CCTCAGCATGGCTGG | 5336 |
| rs35371300 | snp | C/G | 0.146314 | 0.227484 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919280 | ATATTTCTTCTGAGA[C/G]ACAGATTCTTCTAGA | 5336 |
| rs35386949 | snp | A/C | 0.330714 | 0.236612 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855958 | CTCTGTCTCCTTAGC[A/C]CCACCTGCAGGCTGA | 5336 |
| rs35400295 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876039 | TTTTTTTTTTTTTTG[G/T]TTTTGAGACAGGGTC | 5336 |
| rs35401283 | snp | C/T | 0.12932 | 0.218944 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928926 | CATCTGTGTTTCCCA[C/T]GCGTTGCGAAGGAAA | 5336 |
| rs35401648 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866191 | TCCCTTGCTCCCAGG[A/G]TGAGCTCCACTGGGG | 5336 |
| rs35408572 | in-del | -/G | 0.477853 | 0.102875 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932258 | GTTTGCATCCTGGCA[-/G]GGGCTGGACCCTGGG | 5336 |
| rs35408759 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941084 | TTTGATATTGTTTGG[-/G]AAACGTGGGGCTCAA | 5336 |
| rs35433145 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865858 | CCAGGGTGAGCTCCA[-/A]CTGGGGCACCAGCAT | 5336 |
| rs35441116 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81819488 | GGACCTCCTGGCTCC[-/C]TCGCCCACTGCTTTT | 5336 |
| rs35454747 | snp | G/T | 0.125874 | 0.217008 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878975 | CAGAGTGTCCGGGCA[G/T]GGAGTTGCAAGACCT | 5336 |
| rs35459651 | snp | C/T | 0.487684 | 0.0775019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899622 | ATCTGTTGACTGCCA[C/T]GTTTTTCCTGTTTTT | 5336 |
| rs35474393 | in-del | -/AA | 0.385359 | 0.210185 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857095 | TTACTTTAAGTCACT[-/AA]GTTTGTGGTCATTTG | 5336 |
| rs35520613 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866339 | CAGCATGAGAGGACG[-/C]TGGCCTCTCCCTTGC | 5336 |
| rs35529016 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866172 | ATGAGAGGACGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs35542948 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816568 | CTACTGCCTTGACCT[-/T]CCTGGGCTCAAATGA | 5336 |
| rs35554443 | snp | C/G | 0.331411 | 0.236373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856017 | AGGAGACCAGAAGAA[C/G]CCGGGTCTTGGAAGC | 5336 |
| rs35558572 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797849 | GTCTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 5336 |
| rs35559608 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916298 | CTTTTTTAAAAAAAG[-/A]AAAAAAACAACGTTT | 5336 |
| rs35563165 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866491 | ATGGGCTCCACTGGG[-/G]CACCAGCATGAGAGG | 5336 |
| rs35610796 | snp | C/T | 0.187053 | 0.241946 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853661 | ATAGTGCTTACTTGC[C/T]GGTACCAGTCCATGG | 5336 |
| rs35658502 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866706 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGCACC | 5336 |
| rs35665271 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915342 | TGGATAGATTTCCCC[-/C]AGTAGAGGAGAAACA | 5336 |
| rs35692238 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789709 | ATTATAATAAGTCCC[C/T]CGGATGGTCTGATAA | 5336 |
| rs35719880 | snp | C/G | 0.151001 | 0.229563 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919170 | TGGGACACATTTGGC[C/G]TACTCTTGACCTAGT | 5336 |
| rs35747119 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81834285 | TTCTCTGTCCCAGTA[-/A]GGTGTTTCTGCCCTG | 5336 |
| rs35770398 | snp | C/G | 0.479583 | 0.0989539 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933735 | CACCCCCCAAACAGT[C/G]ACCATTATTATCTAA | 5336 |
| rs35800368 | snp | C/T | 0.367503 | 0.220665 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912361 | GTGAACCACTGTGCT[C/T]GGCCCAATGTATTAT | 5336 |
| rs35806969 | in-del | -/T | 0.488241 | 0.0757703 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868370 | TAAAAGAAACCTTTA[-/T]TTTTTTTACTTATTT | 5336 |
| rs35819356 | snp | A/G | 0.474363 | 0.110278 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885172 | GCTGGGATTGCAGGC[A/G]TCTGCCACAACACCT | 5336 |
| rs35825904 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866143 | CCAGGATGAGCTCCA[-/A]CTGGGGCACCAGCAT | 5336 |
| rs35847871 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841082 | AATCTCTTCACATGG[-/G]AAGCAGGACACTGAT | 5336 |
| rs35911557 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81937701 | CTAGAAACTCCTGGC[-/C]TAGGGGGCCAGCGTG | 5336 |
| rs35916156 | snp | G/T | 0.470521 | 0.117772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888396 | AAAGAAAAAAAAAAT[G/T]TTTGTATTTTAGTAG | 5336 |
| rs35946344 | in-del | -/TTCT | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857640 | AGCTCTAGTCTCTCT[-/TTCT]CTTCTCTAAAAAGGC | 5336 |
| rs35966072 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854054 | ACAGTTGACCTTTAG[-/G]CTGCCTAGAGTGATC | 5336 |
| rs35978156 | in-del | -/A | 0.398174 | 0.201356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797282 | GGTGAATCATTTTTG[-/A]AAAAAAAAAAATTAT | 5336 |
| rs35985234 | snp | G/T | 0.459184 | 0.136902 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866239 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGGGCT | 5336 |
| rs36023013 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934945 | CACCCCCATGATTCA[A/G]TTATCTCCTATCGGG | 5336 |
| rs36028855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866166 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs36033508 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777387 | ATATAACACATACTA[-/T]AAACAAAAGTGTGAA | 5336 |
| rs36034802 | snp | C/T | 0.322721 | 0.23919 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810644 | TTCTGCAATTTCTTT[C/T]TTTTTATTTTTTGCT | 5336 |
| rs36036965 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916289 | CTGGAAATCCTTTTT[-/T]AAAAAAAGAAAAAAA | 5336 |
| rs36082804 | snp | C/T | 0.277867 | 0.248442 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788429 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 5336 |
| rs36085277 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830194 | GCATGTTGGCACGCA[C/T]CTGTGGTCCCAGCTA | 5336 |
| rs36096723 | snp | C/G | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779098 | TTGCCTCAGTTTCTT[C/G]TTTGGCACGCAGAGG | 5336 |
| rs36112575 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835224 | TAGGGTGGCTGGCAC[-/C]GAAATGGGATAATTT | 5336 |
| rs36114479 | snp | C/G | 0.107694 | 0.205546 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858185 | TCCCATCTTCGTGAT[C/G]TGTATGGGGCAGGGC | 5336 |
| rs36116027 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886751 | ATTTATATAACATGG[-/G]AGAATAACCTGTACC | 5336 |
| rs36117302 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822285 | TGAAGGGTCGGCATA[A/G]GTGGTAAGCATGATT | 5336 |
| rs36126447 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885069 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTCTTGC | 5336 |
| rs41301799 | snp | C/G | 0.120326 | 0.21374 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869141 | TGCCTGAGGTGGGAA[C/G]TGATGGGAGCAGCTA | 5336 |
| rs41301803 | snp | A/G | 0.174288 | 0.23826 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907555 | TTCAGAGAATTCGCC[A/G]TAAATGTCTATGAAA | 5336 |
| rs41303769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854805 | TGAAATGGGGAGAAT[A/G]ATAATGCCTATTTCA | 5336 |
| rs41305759 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854669 | ATAGCAGAATGCTCA[A/C]CCCTGCCTGCTCACT | 5336 |
| rs41305761 | snp | A/C | 0.151668 | 0.229849 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881014 | CGGTGCCTGGTGCCC[A/C]GCCGGCCTCCAGGAG | 5336 |
| rs41305763 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927346 | AAATTGAGATTGAGT[A/T]GTTGTGGGTGAGTTG | 5336 |
| rs41305765 | snp | A/C | 0.147778 | 0.228146 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912763 | CAGAGGGGCTTGGCA[A/C]GGACAGATGCGGAGA | 5336 |
| rs41307919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854802 | CTGTGAAATGGGGAG[A/G]ATAATAATGCCTATT | 5336 |
| rs41307921 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923348 | AATGCCAGTCCCTCT[A/C]CAGCAGATGACTTTG | 5336 |
| rs41309272 | snp | C/T | 0.233527 | 0.249457 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859290 | GTCCATTGTGATCTG[C/T]GGATGCCATGTTGGG | 5336 |
| rs41309274 | snp | C/T | 0.0278269 | 0.114628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880999 | GGCTGTGCCGGACCT[C/T]GGTGCCTGGTGCCCA | 5336 |
| rs41311268 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907888 | CTGGCAAGGGGATGC[C/T]CCGCTGAAGAAGCTG | 5336 |
| rs41311270 | snp | C/G/T | 6.68923e-05 | 0.00578293 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937920 | TAAAGCCAGCCCTCC[C/G/T]TTCCTGCCAGGGGAG | 5336 |
| rs41311272 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923394 | GCCTCCTGCTCCCCA[A/G]TGAGAAGAACCAAAT | 5336 |
| rs41312260 | snp | C/G | 0.11963 | 0.213316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870663 | AATGTTGTAGAAAAG[C/G]CATGTTAAATAGCAT | 5336 |
| rs45443101 | snp | A/T | 0.0824224 | 0.185525 | missense | PLCG2 | GRCh38.p7 | 16:81889176 | GTCATTTTAAGGAGC[A/T]TTGGGCTCAGGATCT | 5336 |
| rs45482302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957166 | TAGCTGGGCATGGTC[A/G]TGGGCGCCTGTAATC | 5336 |
| rs45491692 | snp | G/T | 0.0579916 | 0.160105 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956900 | TCAGCCCCTCCACCT[G/T]CAAAAACTTTTGGGG | 5336 |
| rs45551535 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928736 | CCTGTCTTGAATGCC[A/G]GCTCCTTCCCTGGCT | 5336 |
| rs45554137 | snp | C/T | 0.0446916 | 0.142648 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958033 | AGGGTATTGTGTGTG[C/T]GCGCATGTGTGTTTG | 5336 |
| rs55637504 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793277 | GGAGCTTGTGGTACT[A/G]TTGGGCATGTTGGTT | 5336 |
| rs55638712 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795711 | CTGCTTTTTTTTTTT[C/T]TCCCCAAGAGATGGG | 5336 |
| rs55645129 | snp | A/G/T | 0.00824292 | 0.063669 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912583 | TGGTCGTTTTCCCTG[A/G/T]CCCTGTGCCGCAGGT | 5336 |
| rs55649358 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836171 | CTAGTGTTTTCATAC[C/G]CTAGAGACTATCCAA | 5336 |
| rs55653847 | in-del | -/CCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803639 | CTTTTCTTCTTCCCT[-/CCC]TCCCTCCCTCCCTCC | 5336 |
| rs55678733 | snp | C/T | 0.177182 | 0.23916 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860234 | TTTAAAAAAAGCAAA[C/T]GCAGTTTTGGTTTTT | 5336 |
| rs55683592 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955475 | TCATCCTCCCCCTGC[A/C]TTGAAACCCAAACTC | 5336 |
| rs55684799 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865834 | AGGATGCTGGTCTCT[C/T]CCTTGCTCCCAGGGT | 5336 |
| rs55687320 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820582 | CATGGGAGATCTTGG[A/G]CATATCAGTTTTCCC | 5336 |
| rs55696133 | snp | A/C | 0.25634 | 0.24992 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954506 | TGCATTCCCCATCCG[A/C]CAACTAGCCATGGTG | 5336 |
| rs55711872 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891300 | TGTCGCTGCAGCCCA[C/T]TGCAGCCTGAGCCTT | 5336 |
| rs55726664 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906925 | TGCCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA | 5336 |
| rs55737025 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803625 | TTTTCTTTTCCTTTC[C/T]TTTCTTCTTCCCTCC | 5336 |
| rs55759329 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865832 | AGAGGATGCTGGTCT[C/T]TCCCTTGCTCCCAGG | 5336 |
| rs55768769 | snp | G/T | 0.453453 | 0.145282 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782691 | CAGAAATCAAGGAAG[G/T]TTTTCTCTTCAGTGC | 5336 |
| rs55791328 | snp | C/T | 0.17138 | 0.237316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862560 | TTGCTTTTCCTTTTT[C/T]CTTTTTTCTTTTTTT | 5336 |
| rs55797469 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862726 | AGTACAAAAAAGTTA[A/G]CTGGGTGTAGTGGTG | 5336 |
| rs55801253 | snp | A/G | 0.160938 | 0.233598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863296 | ATAAGTGGACTAGCA[A/G]AATATTTGTCCTTTT | 5336 |
| rs55809736 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861823 | GTTTGTGAGGTCAAG[A/G]AATGGATACCACCCT | 5336 |
| rs55822905 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872056 | AATACAGGCCAGGTG[C/T]AGTGGTTGACGCCTG | 5336 |
| rs55824979 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803522 | TTTTCTTTGTTCTTT[C/G]TTTCCTTTCTTTCTT | 5336 |
| rs55829397 | snp | C/T | 0.23846 | 0.249734 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855861 | GTAGGAAATGAGGAG[C/T]GAATGTCTGACTGAT | 5336 |
| rs55833904 | snp | A/G | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825259 | TGCTCTAATCTTTTA[A/G]ATTAGATCTGAAGAG | 5336 |
| rs55835147 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855618 | TGCCGCCTTTAAGAA[A/G]CTCTCAGTCGACTTG | 5336 |
| rs55848326 | snp | C/T | 0.459914 | 0.13578 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782696 | ATCAAGGAAGTTTTT[C/T]TCTTCAGTGCTCTGT | 5336 |
| rs55850521 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803632 | TTCCTTTCTTTTCTT[-/C]TTCCCTCCCTCCCTC | 5336 |
| rs55856197 | snp | C/T | 0.314057 | 0.241654 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853618 | ATCTGATGCCGCTGC[C/T]GATCTGACAGTTGGT | 5336 |
| rs55866072 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829610 | CAGAATTTATTTGGA[C/T]TTTAACAGTTTCTCC | 5336 |
| rs55873405 | snp | C/G | 0.499693 | 0.0123764 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872227 | CAGCTACTTGGGAGG[C/G]TAAGGCAGGAGAATC | 5336 |
| rs55876216 | in-del | -/CCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803647 | CTTCCCTCCCTCCCT[-/CCC]TCCCTCCCTCCCTCC | 5336 |
| rs55880431 | snp | C/G | 0.402454 | 0.198136 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943852 | CCCCATAAACCCTAC[C/G]AGGAAATGAGTGGGT | 5336 |
| rs55885812 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801022 | AGGAACTCATTCTCC[C/G]CTAGAGGGTCTGGAG | 5336 |
| rs55901360 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829613 | AATTTATTTGGACTT[C/T]AACAGTTTCTCCTCG | 5336 |
| rs55909816 | snp | A/C | 0.395087 | 0.203592 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862918 | AACAACGAAAATAAA[A/C]ACAATTGTGCTGTTG | 5336 |
| rs55931921 | snp | A/G | 0.150667 | 0.229419 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836047 | GGACTGGACTTCTAT[A/G]TATGTTTTTGGGGGA | 5336 |
| rs55936247 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858872 | TTTTGGGGATTAAAT[G/T]ACTATCATCAGAAGG | 5336 |
| rs55939012 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840224 | GAGAGCATGCTTAGA[A/T]TTGAGCCCTGACAGC | 5336 |
| rs55939349 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800665 | ATTGTGATACTATTG[C/T]TATTATTATTATTAT | 5336 |
| rs55943110 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944859 | GTCCCCCATAGATAT[C/T]AAGGGCCAACTGTAG | 5336 |
| rs55997054 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837841 | TAATATCTTGCAAAC[A/C]TGTAGTGCAGTATCA | 5336 |
| rs56017659 | in-del | -/TACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899289 | ATATATATATATATA[-/TACA]CACACACACACATAA | 5336 |
| rs56018718 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882538 | GGCGGGTGGTGTGTC[A/G]AGCCCTGTCTGGGTA | 5336 |
| rs56019161 | snp | C/G | 0.0919752 | 0.193722 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849612 | AGAAATACACATACA[C/G]ACACACAAATTTTCC | 5336 |
| rs56026444 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778032 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAACAAAA | 5336 |
| rs56027201 | in-del | -/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778030 | CAAAAAAAAAAAAAA[-/C]ACAAAAAAAAAACAA | 5336 |
| rs56045537 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882006 | GACTGTGAGGCTGGT[C/G]GGGAAAGGTTAGAAT | 5336 |
| rs56047457 | snp | A/G | 0.160938 | 0.233598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863338 | ATTTCACTTAGTGTA[A/G]TGTCTCCAAGTTTCA | 5336 |
| rs56051434 | snp | G/T | 0.0785177 | 0.181917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816774 | CCCAAAATGCTGGGA[G/T]TACAGGCATTAGCCA | 5336 |
| rs56052823 | snp | C/G | 0.324855 | 0.23853 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952752 | GTAGAAGGAATGAGG[C/G]AACTAGAAAATCACT | 5336 |
| rs56054659 | snp | A/T | 0.429388 | 0.174127 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863242 | AAATCACCACTCTAC[A/T]GTCTGTCTCTCTGGA | 5336 |
| rs56070867 | snp | A/G | 0.163564 | 0.234582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869158 | GATGGGAGCAGCTAA[A/G]TCCTGTGCTGTTGAA | 5336 |
| rs56075600 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787558 | TTTTTTTTATAATAG[A/G]TTGATTGAGACATAA | 5336 |
| rs56099607 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860169 | ATTATTATTATTATT[A/T]TTATTTTTTTTTTTT | 5336 |
| rs56104329 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902669 | CTCTACCCTCATTCC[C/T]GTTCATGAGGACTCT | 5336 |
| rs56105557 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957378 | AGAAATTAACCTACA[C/G]TAATACCTTAGGCGC | 5336 |
| rs56117891 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827965 | CATGGTGGCGGATGC[C/T]TGTAATCCCAGCTCT | 5336 |
| rs56120990 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862736 | AGTTAGCTGGGTGTA[A/G]TGGTGCACATTTGTA | 5336 |
| rs56134131 | snp | A/G | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824952 | AAGGTAGGAGGTCAC[A/G]GTCAGGGAGAGAGAG | 5336 |
| rs56151509 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803506 | TTGGTTACTGTTTTC[A/G]TTTTCTTTGTTCTTT | 5336 |
| rs56186502 | snp | A/C | 0.477768 | 0.103061 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793987 | TGTGTGTCATAAACA[A/C]CCTGCCTGAGACCAA | 5336 |
| rs56188311 | snp | C/T | 0.291493 | 0.246533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852655 | CGGAAGGATTTCTTA[C/T]TTGTTTCTGTTATCT | 5336 |
| rs56204860 | snp | A/C | 0.0952156 | 0.196321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827800 | TCATTTAAAAAAAAG[A/C]GTTGACGCCGCCAGG | 5336 |
| rs56215311 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872287 | GAGCCGAGATTGCAC[C/T]ACTGCACTCCAGCCT | 5336 |
| rs56226199 | snp | A/T | 0.190833 | 0.242898 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807578 | GAGCTTTCCCTGTAT[A/T]ATTGCTTACTTAATT | 5336 |
| rs56237642 | snp | A/G | 0.118235 | 0.212457 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814795 | GTTCCCTTGCTGTGT[A/G]ACCACAGGGAGTTAA | 5336 |
| rs56242390 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925912 | AAAAAAAATCCAGAA[A/G]GATATCATATAGAGG | 5336 |
| rs56256532 | snp | A/G | 0.133093 | 0.220981 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927602 | GACTTTGCAAACCTG[A/G]TGGTTGTTCCCTCGC | 5336 |
| rs56258157 | snp | C/G | 0.499722 | 0.0117779 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909331 | TGTGAAAGTCTGTGA[C/G]GAAGGCTCTGATGCC | 5336 |
| rs56260145 | in-del | -/AT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860174 | ATTATTATTATTATT[-/AT]TTTTTTTTTTTTTGT | 5336 |
| rs56274468 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908987 | AGCATCTCTGTCTCC[G/T]CCATAAAACGAGGAC | 5336 |
| rs56306585 | snp | G/T | 0.0770498 | 0.180522 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959110 | TAAAGGAGAGGAGAG[G/T]GCTGGGTTGGGAAGG | 5336 |
| rs56309621 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906937 | CAGCTACTCAGGAGG[A/C]TGAGGCAGGAGAATT | 5336 |
| rs56314015 | snp | A/C | 0.181442 | 0.245137 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868789 | TGAATCTCCTGCAAG[A/C]CCTTCCTCCATGACC | 5336 |
| rs56330703 | snp | C/T | 0.395635 | 0.2032 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862914 | CAAAAACAACGAAAA[C/T]AAAAACAATTGTGCT | 5336 |
| rs56350744 | snp | G/T | 0.45645 | 0.140991 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780803 | AGGCCGAGCTGGGCT[G/T]ATCACTTGAGGTCAA | 5336 |
| rs56357446 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839779 | ATTTAGGCTGGGCAT[A/G]GTGGCTCATGCCTGT | 5336 |
| rs56397554 | snp | C/T | 0.17138 | 0.237316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862331 | GGCAAATGGTAGCAG[C/T]GGGCATTTGTTTACA | 5336 |
| rs56676680 | snp | C/T | 0.163236 | 0.234461 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868496 | TTCTGCCAAGCCCGT[C/T]CTGTGGTTTTGGTTC | 5336 |
| rs56697259 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907055 | AAAAAAAAAAAAAAA[-/A]CAGTGCAGCACACCA | 5336 |
| rs56698225 | snp | A/G | 0.131091 | 0.21991 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888384 | CCAAGCTGATTTAAA[A/G]AAAAAAAAAATGTTT | 5336 |
| rs56704282 | snp | A/C | 0.237593 | 0.249692 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778378 | CTGCCTCTTAGAAAA[A/C]AGAAGCTATAACTCA | 5336 |
| rs56724202 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844125 | GGGACTACAGGTGCC[C/T]GCCACCACACCCGGC | 5336 |
| rs56728944 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934851 | GAGAGAATGAGAAGC[A/G]AGTGAAAGGGGAAAC | 5336 |
| rs56731562 | snp | C/T | 0.100231 | 0.200173 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929308 | CTCCCTGGGCAGGCA[C/T]GGGCATGCTCCCCTA | 5336 |
| rs56781211 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875396 | GGCCTGTTTACTGCA[C/G]GGTAGTAAGCTGCAG | 5336 |
| rs56943275 | snp | G/T | 0.287867 | 0.247116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864547 | GATTTAATTTCTGTG[G/T]GCCTCAGTTTCCTCA | 5336 |
| rs56958555 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860175 | TTATTATTATTATTT[-/A]TTTTTTTTTTTTGTA | 5336 |
| rs57004254 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873334 | ACAACAAAAACCATG[A/G]TTCATAAAAGCTTAT | 5336 |
| rs57033736 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904934 | ACTCTGTTGCCCAGG[A/C]TGGAGTGCAGTGGTG | 5336 |
| rs57123466 | snp | A/C | 0.0865458 | 0.189163 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875765 | GCACTTGCAAAAAAT[A/C]AAAAAGAAAATTGAG | 5336 |
| rs57156891 | snp | A/G | 0.164873 | 0.23506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810336 | AGAACACGTAACGTG[A/G]CCATGAGCAGCCTCA | 5336 |
| rs57169896 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860053 | ATAGCTCGCTGCAGC[C/G]GTAAAGTCCTGGGCT | 5336 |
| rs57195186 | snp | C/T | 0.130008 | 0.219321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904554 | CCGGTCGCCTTAGTC[C/T]AATCCCCATTGGGTC | 5336 |
| rs57205838 | in-del | -/G | 0.499971 | 0.00379382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916593 | CCATTTTTTTTTTGT[-/G]TGTGGTGAGACTTAA | 5336 |
| rs57252573 | in-del | -/CAGGCCAGGCATGGTGGCTCA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957015 | GGGCATGGTGGCTCA[-/CAGGCCAGGCATGGTGGCTCA]TGCCTGTAATCCCAG | 5336 |
| rs57305207 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81917245 | TTTTTTTTTTTTTTT[-/T]AAAGCAAATGGTATT | 5336 |
| rs57345006 | snp | G/T | 0.49925 | 0.0193545 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844385 | CAGTGGTGTGATCTT[G/T]GCTCACTGCAACCTC | 5336 |
| rs57346304 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818906 | TTTTTTTTTTTTTTT[-/TT]ACTGTGGTGGGGCTC | 5336 |
| rs57375866 | in-del | -/CACACACACACACACACACACACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896403 | ACACACACACACACA[-/CACACACACACACACACACACACA]AATCATCTGGGTGTA | 5336 |
| rs57480004 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787752 | TCCCCCCTACCAGAC[A/G]TAAGCAACCGTTAAA | 5336 |
| rs57503200 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878139 | AGGCGCCCACCACCA[C/T]GCCTGGCTAATTTTT | 5336 |
| rs57508298 | in-del | -/A | 0.457853 | 0.138915 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816062 | AAAAAAAAAAAAAAA[-/A]TGTGCCTTCACGGAC | 5336 |
| rs57522760 | in-del | -/CC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789851 | CACCTTTGCCCCCCC[-/CC]TCCATTGCCTCCCCT | 5336 |
| rs57582517 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861583 | CTGGGCCACCCTCTC[A/G]TGTTACTGAGGTGGA | 5336 |
| rs57586664 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955518 | GGCTTTTGTCTTTTT[C/T]TCTCCCCTAGCGTAA | 5336 |
| rs57620642 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849646 | TCTGGTGGCGGATGC[C/T]TGTAATCCCAGCTAC | 5336 |
| rs57626691 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807939 | GAGATGGTGCAAAAC[C/T]GTTAATGAGCAATTC | 5336 |
| rs57747833 | snp | C/G | 0.0722614 | 0.17581 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784499 | TGAACACCAGCCTCT[C/G]ACTCCTCCTTCTTTG | 5336 |
| rs57760666 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830975 | GGTGACAACCTTGCT[C/G]TTCCTACAACCAACC | 5336 |
| rs57770941 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875390 | GCTGAAGGCCTGTTT[A/C]CTGCAGGGTAGTAAG | 5336 |
| rs57775883 | snp | A/G | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866419 | TCCCTTGCTCCCAGG[A/G]TGAGCTCCACTGGGG | 5336 |
| rs57784877 | in-del | -/A | 0.322721 | 0.23919 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810650 | AATTTCTTTCTTTTT[-/A]TTTTTTGCTGGTGAT | 5336 |
| rs57789903 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875303 | TAATTCCCCCCTAGA[A/G]GCCTGTGCAAGAGCT | 5336 |
| rs57816646 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878227 | CTGACCTAGTGATCC[A/G]CCTGCCTCGGCCTCA | 5336 |
| rs57838502 | snp | G/T | 0.32955 | 0.237006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802380 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA | 5336 |
| rs57963515 | snp | C/G | 0.148661 | 0.22854 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832965 | CCAGCTTGCTGCTGG[C/G]GCCATGACAGTAACT | 5336 |
| rs57992422 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839906 | AAAGAGAAAACTTAG[C/G]TAGGTGTGATGGTGC | 5336 |
| rs58039411 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866362 | TCCCTTGCTCCCAGG[A/T]TGAGCTCCACTGGGG | 5336 |
| rs58124292 | snp | A/G | 0.382666 | 0.211895 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856830 | TATCCTGGACTATCT[A/G]GGTGTCTAGTGGAAT | 5336 |
| rs58132126 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866479 | CTTTCTCCCAGGATG[A/G]TCTCCACTGGGGCAC | 5336 |
| rs58137789 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836197 | TCCAAATGACACAGC[C/T]GACCCAATCCCTGCA | 5336 |
| rs58159952 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858509 | ATGGGTGCCTAGTAG[C/T]GGTGTGGGCTCTACA | 5336 |
| rs58171961 | in-del | -/GTGTGT | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830662 | GGTGTGTGTGTGTGT[-/GTGTGT]ATATATATATATACA | 5336 |
| rs58191847 | in-del | -/AATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911623 | ATTAATTAATTAATT[-/AATT]TTGAGACCGGGTCTC | 5336 |
| rs58224015 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866587 | TCTCCCTTGCTCCCA[A/G]GATGAGCTCCACTGG | 5336 |
| rs58227801 | snp | A/G | 0.216048 | 0.247684 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908830 | CAAAAGTAATGCAAA[A/G]AAGTCTGTGATGAAC | 5336 |
| rs58245322 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874001 | GAACCCTCTGGGGTG[C/G]CCTAGATTGCCCCGT | 5336 |
| rs58257849 | in-del | -/TT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892864 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC | 5336 |
| rs58265888 | in-del | -/CACACACACACACACACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896409 | ACACACACACACACA[-/CACACACACACACACACA]AATCATCTGGGTGTA | 5336 |
| rs58271299 | snp | A/C | 0.487871 | 0.076925 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777977 | AGCCGAGATCGTGCC[A/C]CTGCACTCCAGCCTG | 5336 |
| rs58297070 | snp | A/G | 0.0451351 | 0.144624 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878429 | TATTAGGACTTGGAC[A/G]TATATTCCCGGGGAC | 5336 |
| rs58370747 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917697 | TCCTTTGAGAAATGT[C/G]TATTCAGATCCTTTG | 5336 |
| rs58431500 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899699 | TGGTGAGGGCTGCCT[C/G]GTGTTCCTGAGCAGG | 5336 |
| rs58444993 | snp | C/T | 0.105924 | 0.204309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787851 | TTTTGTGACTGGCTT[C/T]TTTGACTCAGCATTT | 5336 |
| rs58472307 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866455 | GCATGAGAGGACGCT[A/G]GCCTCTCCCTTTCTC | 5336 |
| rs58621683 | in-del | -/GG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925459 | AATGGTGCGGGGGGG[-/GG]CGTGAAAAGGGCTTA | 5336 |
| rs58630618 | snp | C/T | 0.089084 | 0.191327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902119 | TGTCCCGTCCTTTTC[C/T]CTACTGTTCTGTGCA | 5336 |
| rs58671817 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933004 | TCTCCAAATAGTGCA[C/T]TCCAGCTCTCTCTAC | 5336 |
| rs58737360 | snp | A/G | 0.143284 | 0.226079 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907071 | CAGTGCAGCACACCA[A/G]CATGGCACATGTATA | 5336 |
| rs58739440 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878410 | CATGCCCATGGGTAC[C/T]GGGTATTAGGACTTG | 5336 |
| rs58758762 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787491 | CCTTGGCCTCCCAAA[A/G]CATTGGGATTACAGG | 5336 |
| rs58759555 | in-del | -/ATTT | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778830 | TTTATTTATTTATTT[-/ATTT]TTGAGACGGAGTGTC | 5336 |
| rs58793678 | in-del | -/AACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939609 | CCTGCTCTGCAAACA[-/AACA]CCTCCCCCGTTCCCT | 5336 |
| rs58848563 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866452 | CCAGCATGAGAGGAC[A/G]CTAGCCTCTCCCTTT | 5336 |
| rs58899768 | snp | A/T | 0.0991586 | 0.199366 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839476 | ATAGGCTGTATATAA[A/T]GTAATGAGCCCTTCC | 5336 |
| rs58902813 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836381 | CAAGAGGTTTTTGCT[C/G]TCTGCAGGGGAGAGC | 5336 |
| rs58979839 | in-del | -/GCTTGTCTCTGATTGGCTGGCTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907933 | ACCATGTCCTGGCTG[-/GCTTGTCTCTGATTGGCTGGCTG]CCCCAGGTGCTTTAA | 5336 |
| rs59055279 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81817981 | ACAGATTCTGGGAGG[A/G]AAGGGGCAAGATTAG | 5336 |
| rs59068951 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871981 | TGTGACATTTTGTGA[C/T]GAAAGCCAGCAGCAG | 5336 |
| rs59090454 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839777 | ACATTTAGGCTGGGC[A/G]TGGTGGCTCATGCCT | 5336 |
| rs59187909 | snp | G/T | 0.133093 | 0.220981 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904563 | TTAGTCTAATCCCCA[G/T]TGGGTCCCCCGCCAC | 5336 |
| rs59207660 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789635 | TCTTTATTTCCTTCT[G/T]CTTTCTCCCTGGAGA | 5336 |
| rs59222730 | snp | A/C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862488 | GTGACTTGACTAAAG[A/C/T]AGCCCAGGTTGTCAG | 5336 |
| rs59256266 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866592 | CTTGCTCCCAAGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs59296782 | snp | C/G | 0.0952156 | 0.196321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933441 | AGCCACCTCATTGAT[C/G]GCAGAGGGCAGTCAC | 5336 |
| rs59300746 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887132 | TGTTTTTTTTTTTTT[-/T]CTTTTGAGATGGAGT | 5336 |
| rs59380456 | in-del | -/CAAGATGCTGGAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857511 | TGGGAATGCCAAGAT[-/CAAGATGCTGGAT]GGTTGAGTTCTGGTG | 5336 |
| rs59430264 | snp | A/T | 0.124491 | 0.216211 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860178 | ATTATTATTATTTTT[A/T]TTTTTTTTTGTAAAG | 5336 |
| rs59433978 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849651 | GCGGATGCCTGTAAT[-/T]CCCAGCTACTCGGGA | 5336 |
| rs59551811 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866467 | GCTAGCCTCTCCCTT[G/T]CTCCCAGGATGAGCT | 5336 |
| rs59598748 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789860 | CCCCCCCTCCATTGC[C/T]TCCCCTCTGTCATTT | 5336 |
| rs59716859 | in-del | -/ATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800690 | ATTATTATTATTATT[-/ATT]GTTATTTCCAACCCT | 5336 |
| rs59725126 | snp | A/G | 0.362523 | 0.223246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879645 | TATGTCGTTAGCATT[A/G]ATCATGTGATAGTGG | 5336 |
| rs59756058 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836099 | ACCCGTTTATACTTT[A/C]TTTCCAGGGCCACCA | 5336 |
| rs59773113 | snp | A/G | 0.198324 | 0.244601 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905714 | CCCAGGCTGGAGTGT[A/G]GTGGTGTGATTGCGG | 5336 |
| rs59786855 | snp | G/T | 0.341685 | 0.232581 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841678 | GGAGAGAAAGAGCTG[G/T]ATTTAACTCATGCCT | 5336 |
| rs59929735 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842842 | ACGTACGGAGGGGCC[A/C]AAAGTCCGCAAGGCT | 5336 |
| rs59930088 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866377 | TTGAGCTCCACTGGG[-/G]CACCAGCATGAGAGG | 5336 |
| rs59970301 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822781 | AAAAAAAAAAAAAAA[-/AAAAAAA]GAAAAAGGCAGGAGA | 5336 |
| rs59993558 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885992 | GGGCACAGTCACGTT[A/C]GGTCTGAGCTGGTGC | 5336 |
| rs60106368 | snp | A/G | 0.471196 | 0.1165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849203 | GCCTGTTTGTATTTC[A/G]TAAGGTGACTGTGGG | 5336 |
| rs60183943 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844165 | TTTTTTTTTTTTTTT[-/TT]GGTATTTTTAGTAGA | 5336 |
| rs60230971 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791715 | GATTACAGGTGGGTA[A/C]CATCACATGCAGCTA | 5336 |
| rs60288994 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893049 | TATTTTTAGTAGAGA[C/G]AGAATTTCACTATGT | 5336 |
| rs60300034 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866565 | ACCAGCATGAGAGGA[C/T]GTGGCCTCTCCCTTG | 5336 |
| rs60305784 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849797 | AAAAAAAAAAAAAAA[A/C]CCAAAAAAATTCCCT | 5336 |
| rs60349380 | in-del | -/GAA/GAAA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925894 | TGTCTCAAAAAAAAA[-/GAA/GAAA]AAAAAAAAAATCCAG | 5336 |
| rs60350318 | snp | A/C/G | 0.0618563 | 0.164627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788063 | TGGATGTCTGTTTTT[A/C/G]TTTGTTTTGGGTATA | 5336 |
| rs60379026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866108 | ACCAGCATGAGAGGA[C/T]GCTGGTCTCTCCCTT | 5336 |
| rs60395073 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929848 | TTTGGGCAGGGGGGT[A/G]CAGGATCCCTGCATC | 5336 |
| rs60408934 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866428 | CCAGGATGAGCTCCA[-/A]CTGGGGCACCAGCAT | 5336 |
| rs60427389 | snp | C/T | 0.388398 | 0.208197 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896322 | CTGAGGTCAGGAGTT[C/T]GAGAAGAGCCTGGGC | 5336 |
| rs60451152 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875567 | GACTTCAGCCATTAT[A/C]ACCTTGTCACTGCCC | 5336 |
| rs60496070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899086 | CTCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 5336 |
| rs60516036 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832112 | TAAATGGAGGGGGGG[-/G]AATAGTGATATTGTG | 5336 |
| rs60541555 | in-del | -/GTCC | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824782 | CATACCCCCAAAGGT[-/GTCC]GTCCATGTCCTAATC | 5336 |
| rs60561476 | in-del | -/CACACACACACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896415 | ACACACACACACACA[-/CACACACACACA]AATCATCTGGGTGTA | 5336 |
| rs60584170 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866365 | CTTGCTCCCAGGTTG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs60594160 | snp | C/G | 0.093777 | 0.195178 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903546 | AAGTGCAGCCACCTG[C/G]CTGGGGTCACAAGTT | 5336 |
| rs60681758 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866422 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs60707451 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787549 | TCTTTTTTTTTTTTT[-/TT]ATAATAGATTGATTG | 5336 |
| rs60780862 | snp | C/T | 0.398894 | 0.200825 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777737 | AACGCTATAACAGGC[C/T]GGGTGCAGTGGCTCA | 5336 |
| rs60883524 | snp | G/T | 5.85406e-05 | 0.00540989 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870966 | AGCAAGTGATCAAGT[G/T]ATGTTTCTGTTTTCC | 5336 |
| rs61048875 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918874 | TTCATGTTTCAAACA[C/G]ATGAAGGAATGAAAG | 5336 |
| rs61066239 | snp | A/G | 0.238749 | 0.249747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813175 | CTTTTTTGGTTCCAT[A/G]TGAAATTTAAAGTAG | 5336 |
| rs61068265 | snp | A/G | 0.364193 | 0.222396 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879583 | ACGTCCTGGGCTGCA[A/G]GGAGTTCAGCAAGAG | 5336 |
| rs61091199 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840250 | ACAGCTGGCCCCTGA[C/G]CTGCCCACCCTGTCA | 5336 |
| rs61092853 | in-del | -/CTTTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803586 | CTTTCCTTTCCTTTC[-/CTTTC]TTTTCTTTTCTCCTT | 5336 |
| rs61098900 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866114 | ATGAGAGGATGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs61132889 | in-del | -/GGG | 0.0532157 | 0.154195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849046 | TAAGAGATGCTTGGA[-/GGG]GGGGCCTGTGTGGGT | 5336 |
| rs61154120 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938665 | AGAAGGTTGCTCCGG[C/G]TTTTCCAGTGAATCT | 5336 |
| rs61198709 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917464 | TAATTTTTTGAGGAA[C/T]CTCTGTACTGTTTTC | 5336 |
| rs61322346 | snp | C/T | 0.249886 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886032 | GTAGAGAGAAATTCA[C/T]GCACTTTTTTCCCTT | 5336 |
| rs61352183 | in-del | -/CCCT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803663 | CCTCCCTCCCTCCCT[-/CCCT]TCCTTCCTTCCTTCC | 5336 |
| rs61370372 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866480 | TTTCTCCCAGGATGG[G/T]CTCCACTGGGGCACC | 5336 |
| rs61374069 | snp | A/G | 0.478271 | 0.101943 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840595 | CATAAAGAGTGTACA[A/G]CCTGGGTCCCTCACA | 5336 |
| rs61398036 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910383 | GGCATGAGCCACTGC[A/G]CCCAGCCTCCTGTGT | 5336 |
| rs61422344 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864291 | AACTCTGGGGCTGCG[C/T]TGTCCAGCAGGGCAC | 5336 |
| rs61472325 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864121 | ATCTGAGCATGCACC[C/G]GAATCCCCTGGAGGA | 5336 |
| rs61501292 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901297 | AGCACTGCAGGGGAG[A/G]TGGGTGATTATATCT | 5336 |
| rs61506152 | snp | C/G | 0.32885 | 0.23724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812496 | GTCTTCTTTTGAGAA[C/G]TGTCTGTTCATATCC | 5336 |
| rs61594082 | snp | A/T | 0.46855 | 0.121392 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918909 | GTTTCTTTTTTTTTT[A/T]AAAAAAAGTCACTGT | 5336 |
| rs61623587 | in-del | -/T | 0.0341408 | 0.126114 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958521 | CTCAGTTCAATGTAC[-/T]TTTAACTACCACCGG | 5336 |
| rs61629968 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866568 | AGCATGAGAGGACGT[A/G]GCCTCTCCCTTGCTC | 5336 |
| rs61635216 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825145 | ATCAGACCTGCATAA[C/T]TGCAAGATGGTAAAT | 5336 |
| rs61687497 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822759 | AGAGCGAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 5336 |
| rs61749044 | snp | A/T | 0.0220113 | 0.102573 | missense | PLCG2 | GRCh38.p7 | 16:81786071 | GAGCTGGGGACGGTG[A/T]TGACTGTGTTCAGCT | 5336 |
| rs61749046 | snp | C/T | 0.000116145 | 0.00761965 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936224 | GAAGGCTGACAGCAT[C/T]ATCAGACAGAAGCCC | 5336 |
| rs61755443 | snp | A/G | 0.00503833 | 0.0499378 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81939992 | CTTTGTGGTTTATGA[A/G]GAAGATATGTTCAGC | 5336 |
| rs61755444 | snp | C/G/T | 0.000496706 | 0.0157522 | missense | PLCG2 | GRCh38.p7 | 16:81858323 | TCTTACACCAGGAAG[C/G/T]GATGAATGCGTCCAC | 5336 |
| rs62043995 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884629 | TGTGTGTACATGTAT[A/G]CATGTCTTTTCACAT | 5336 |
| rs62043997 | snp | A/G | 0.177824 | 0.239355 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887596 | CTTGCACCCATGCAT[A/G]TCACCAGCCTGCTGG | 5336 |
| rs62043998 | snp | C/T | 0.177824 | 0.239355 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887598 | TGCACCCATGCATGT[C/T]ACCAGCCTGCTGGTC | 5336 |
| rs62043999 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890886 | GTATATATGAGGCCG[A/G]GTGCAGTGGCTCACG | 5336 |
| rs62044000 | snp | A/G | 0.107694 | 0.205546 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894171 | TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTC | 5336 |
| rs62044001 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898218 | GGGCTGGAATCATCT[A/C]ACACCTATAGGGCTA | 5336 |
| rs62044002 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903223 | ACAAGGGTGTGGTGG[C/T]GTCAACACGTGGCAT | 5336 |
| rs62044060 | snp | A/G | 0.093417 | 0.194889 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788426 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 5336 |
| rs62044061 | snp | C/T | 0.204189 | 0.245767 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789273 | TAATACCATTTCACT[C/T]GCTTACGCGGATGCG | 5336 |
| rs62044062 | snp | G/T | 0.33693 | 0.2344 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790637 | AGGAGCACCGGCACC[G/T]GGTTTTGGAATAGTT | 5336 |
| rs62044064 | snp | A/C | 0.466412 | 0.125164 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794429 | TCCCCAAGCCCCTGC[A/C]ATGAAGCGTCTCATC | 5336 |
| rs62044094 | snp | C/T | 0.462144 | 0.132269 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803680 | CTTCCTTCCTTCCTT[C/T]CTTTTCTTTCTTTCT | 5336 |
| rs62044135 | snp | G/T | 0.43555 | 0.167544 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821315 | TAATGGATTGTTGTC[G/T]CTTGCTGTGTAACAA | 5336 |
| rs62044136 | snp | C/T | 0.307423 | 0.243316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827567 | CTGCAGGCAGCTGGA[C/T]AGGTGACCTAAATAA | 5336 |
| rs62044137 | snp | C/T | 0.192715 | 0.243348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829354 | CTTCAGGTGATCTGC[C/T]CGCCTCGGCCTCCCA | 5336 |
| rs62044139 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830690 | TATATACACACATAT[A/T]TTTTATATATGTATA | 5336 |
| rs62044140 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830691 | ATATACACACATATA[A/T]TTTATATATGTATAT | 5336 |
| rs62044141 | snp | C/T | 0.203267 | 0.245593 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831012 | ATTTCCATCTTGGGG[C/T]CTTTGCATTTACTAT | 5336 |
| rs62044142 | snp | A/C | 0.194902 | 0.243853 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835363 | CACTTTGGGAGGCCA[A/C]AGCGGGCAGATCACC | 5336 |
| rs62044872 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905808 | GGGACCACACGTGCG[C/T]ACCACCATGCCTGGC | 5336 |
| rs62044874 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908329 | GTTATCTGGTACCCT[C/G]GGTCAGGGTGAGACA | 5336 |
| rs62044875 | snp | A/C | 0.0573587 | 0.15934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909746 | TAACACGCAAATAAT[A/C]CTGGACACCTAAATG | 5336 |
| rs62044876 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909866 | TATCATTCCTGTCAG[A/G]CCGCTGGGGTAGTAA | 5336 |
| rs62044878 | snp | A/C | 0.206947 | 0.246265 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914420 | TGATTCTGACAGGCC[A/C]TCTGGGGATGGGGTT | 5336 |
| rs62044879 | snp | C/G | 0.170408 | 0.236992 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919299 | GATTCTTCTAGATCT[C/G]TTTTGAAAATACCCA | 5336 |
| rs62044880 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922850 | GCAAATTCATTGAAG[A/G]AAATTTCTAACCAAG | 5336 |
| rs62044881 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923732 | TGTGTTAAGTCCCTT[C/T]TTAGGAAGGTGGCTT | 5336 |
| rs62044882 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925080 | CCAAATCACGGTTTT[C/T]CATTCTGTGTGAGAT | 5336 |
| rs62044883 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925397 | GGACAGATGGTATAT[A/G]TGATCGCCGTAAATA | 5336 |
| rs62044884 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925565 | TGTTAAGTTCTTCCC[A/G]CCACCACGGAGCACA | 5336 |
| rs62044885 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925615 | AAGGTCAGCCGGGTG[C/T]AGTGACTTGCGCCTG | 5336 |
| rs62044886 | snp | A/T | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925853 | GATCGTGCCATGCAC[A/T]CCAGCCTGGGGGACA | 5336 |
| rs62044947 | snp | C/T | 0.327445 | 0.237702 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936843 | ATTTAAGACCTCTTT[C/T]GAGGGATCTATTCAT | 5336 |
| rs62044949 | snp | C/T | 0.304188 | 0.244057 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944459 | TATATGCAAATACTA[C/T]GCCACTGAATTAATT | 5336 |
| rs62044950 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949517 | TCAGTGTCCAGCCCC[C/T]GACATGTCAAGGAAT | 5336 |
| rs62044951 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952649 | AGATTCTAGCACACA[G/T]AATGAAATAGCCACA | 5336 |
| rs62045701 | snp | A/T | 0.214843 | 0.247516 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842633 | TGCCCCTTGAGGTCA[A/T]GTATGGGAATTGGGG | 5336 |
| rs62045702 | snp | C/T | 0.196149 | 0.244131 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842689 | GGTGGGAGGACGTTC[C/T]GTGGGTGCAGGGAGC | 5336 |
| rs62045703 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846620 | AACATCGGGCTTATG[A/G]CTAATGCTTAAAAAG | 5336 |
| rs62045704 | snp | C/T | 0.24019 | 0.249807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846791 | ACATTCAATACAGCA[C/T]GAAACACTTCACCTC | 5336 |
| rs62045706 | snp | A/G | 0.251014 | 0.249998 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851810 | GGGCCACCAGTGCCC[A/G]GCTTGTTTTCACATG | 5336 |
| rs62045708 | snp | A/G | 0.190833 | 0.242898 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852406 | AGCTCTATCTAAAGC[A/G]CATGGAATGGGTGCA | 5336 |
| rs62046283 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954579 | TTATGAGTGAGAACA[C/T]ATGGTATTTGGTTTT | 5336 |
| rs62046284 | snp | A/G | 3.31318e-05 | 0.00406999 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956817 | CAACCGGGATGCCCT[A/G]GTTAAAGAGTTCAGT | 5336 |
| rs62046428 | snp | G/T | 0.302936 | 0.244331 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778961 | CCCGGGCGCCCGGCC[G/T]GGAGTGTGTTAAGTA | 5336 |
| rs62046429 | snp | A/G | 0.304937 | 0.243889 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779455 | GGGAGCGAGGCAGGC[A/G]GGGCGCCCAGGGACC | 5336 |
| rs62046430 | snp | C/T | 0.423257 | 0.180228 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779492 | CCGCGGGGACCGGCT[C/T]CCAGGGCGCTGCGTC | 5336 |
| rs62046431 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780734 | TGAGAAAACTTTTGA[A/C]AACATTTCTTGGTCA | 5336 |
| rs62046673 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857272 | CTTCAAGTGATTCTC[A/C]TGAGCAGCTGGGGTT | 5336 |
| rs62046676 | snp | C/T | 0.172351 | 0.237636 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861877 | AGTCCTGCATAGAGA[C/T]CCATCTTCCCATCGG | 5336 |
| rs62046679 | snp | A/G | 0.160938 | 0.233598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863521 | AACATGGGTGTACAA[A/G]TCTGTTTGAGTCTCT | 5336 |
| rs62046681 | snp | C/T | 0.147656 | 0.228091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865110 | CCTGGGCACACCTGA[C/T]GGGGAGCTCTGAGCA | 5336 |
| rs62046682 | snp | A/C | 0.33875 | 0.233717 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868016 | CCTCGCTTCCCGCTT[A/C]AGCTGAACCTCACTA | 5336 |
| rs62046684 | snp | A/G | 0.0600342 | 0.162525 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870842 | GTGGTCACTTTTTTC[A/G]TATTTACAGGAAATA | 5336 |
| rs62046758 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873568 | GTTTTTTTTTTTTTA[A/T]TAATAGTTTACCTTG | 5336 |
| rs62046759 | snp | A/G | 0.132409 | 0.220618 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875367 | CTGAGGTCCAGAGAG[A/G]TTACTTTGCTGAAGG | 5336 |
| rs62047360 | snp | C/T | 0.234982 | 0.249549 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876939 | TGGGATGCTAGAGAT[C/T]TACCAAGGTGGGCCT | 5336 |
| rs62047361 | snp | A/G | 0.365853 | 0.221536 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877266 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCT | 5336 |
| rs62047363 | snp | A/G | 0.154993 | 0.231244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878835 | TGGTTCTCTTGCAGC[A/G]TTTGTGGCTCTTGGC | 5336 |
| rs62047364 | snp | A/G | 0.187053 | 0.241946 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878987 | GCAGGGAGTTGCAAG[A/G]CCTGGCAGAGGAGGG | 5336 |
| rs62047369 | snp | C/T | 0.158302 | 0.232576 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882112 | ATCTCTTACACTATT[C/T]GAAATAGACCTCTTT | 5336 |
| rs62047669 | snp | A/T | 0.211212 | 0.246973 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782245 | TGAGATACAAGAAAA[A/T]CCTTTAGAAGGACAT | 5336 |
| rs62047671 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784171 | GGTCCCTTTGGTATG[G/T]GTGTGCAGTAGAGGG | 5336 |
| rs62047672 | snp | A/G | 0.306431 | 0.243548 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785218 | CCACAAGCATAAACA[A/G]CAATCAAGGACACCT | 5336 |
| rs63166261 | in-del | -/AGAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940716 | TTCCTACACAGCTGA[-/AGAT]GATAGACACTTCCAG | 5336 |
| rs66525407 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870770 | TGCCATTTCTGAAAC[-/A]AAAAATTATTCTATA | 5336 |
| rs66596320 | in-del | -/TA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900108 | AAATGTATGCATGCA[-/TA]CACATGCAAATTACA | 5336 |
| rs66642225 | in-del | -/AGACCCTTTGCTTAGTGAAGC | 0.422158 | 0.181278 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946885 | AACCAGTGAGCATGA[-/AGACCCTTTGCTTAGTGAAGC]AGACCCTTTGCTTAG | 5336 |
| rs66781317 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930763 | AAAAAAAAAAAAAAA[-/A]GCCATTTAAATTATT | 5336 |
| rs66847533 | in-del | -/CAAA | 0.274393 | 0.248807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939603 | CACCTTCCTGCTCTG[-/CAAA]CAAACACCTCCCCCG | 5336 |
| rs66849768 | in-del | -/CTAACCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923246 | CCTAACCCCTAACCC[-/CTAACCC]TTAACCCCAACCCAG | 5336 |
| rs66899140 | in-del | -/AC | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805783 | CAAAAAAAAAAAAAA[-/AC]AAAAAAAAAACAAAA | 5336 |
| rs66912462 | in-del | -/G | 0.499971 | 0.00379382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916591 | AACCATTTTTTTTTT[-/G]TGTGTGGTGAGACTT | 5336 |
| rs66930665 | in-del | -/T | 0.434976 | 0.168179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885054 | CACCATGCCTGACAA[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs67150050 | snp | C/T | 0.498346 | 0.0287064 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916885 | TCTGGTGATCCACCC[C/T]CCTTGGCCTCCCAAA | 5336 |
| rs67157120 | snp | A/G | 0.142947 | 0.22592 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865052 | CATCACCCTGGGGGA[A/G]GGAAGGCAGCTGGAA | 5336 |
| rs67160306 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787411 | AGATCCCATCTCTAC[-/A]AAAAAAAAAAAAAAA | 5336 |
| rs67174651 | snp | A/T | 0.147656 | 0.228091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833786 | TTCCTGGGCTCGAGC[A/T]GTCCTCCTGCCTTGG | 5336 |
| rs67283254 | snp | C/T | 0.160938 | 0.233598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834200 | TCTTCCCAAGATTGG[C/T]GGGAGGATTAAAGAG | 5336 |
| rs67392656 | in-del | -/TTTT | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858448 | AAAAACCAATGTCCC[-/TTTT]TTTTTTTTTCCCCCC | 5336 |
| rs67403373 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925975 | TAAGATGTGGCTGCT[CA/TG]GATGACTGTGGGGAC | 5336 |
| rs67522021 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916961 | GTTATTGACTATAGT[C/T]CCTATGCTGTACCAT | 5336 |
| rs67578856 | in-del | -/AAG/AG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925893 | CTGTCTCAAAAAAAA[-/AAG/AG]AAAAAAAAAAATCCA | 5336 |
| rs67600638 | snp | C/G | 0.418974 | 0.184249 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879260 | CTGATGCCTTCAGCA[C/G]CAGGCTGACTTGGTG | 5336 |
| rs67669940 | snp | C/T | 0.48378 | 0.0885831 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838086 | AAAGATACTAATTTT[C/T]TTTTTTTTTTGAGGC | 5336 |
| rs67684611 | in-del | CACG/TAGCA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866565 | GAGCAAGGGAGAGGC[CACG/TAGCA]TCCTCTCATGCTGGT | 5336 |
| rs67823242 | snp | C/G | 0.431473 | 0.171952 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842764 | GAGCTTGAAGAACAG[C/G]GTCATGGCCCGGCCA | 5336 |
| rs67906512 | multinucleotide-polymorphism | CAGTATGGAC/TAATATGGAT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871899 | CTGCATAATGTCACA[CAGTATGGAC/TAATATGGAT]AGACCATAATTTACC | 5336 |
| rs67969389 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885631 | GATAGAACTTTTTTT[-/T]TTTAAAATATAGCCA | 5336 |
| rs67992648 | in-del | -/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828263 | TTTTTTTTTTTTTTT[-/T]GAGACAGAATCTTGC | 5336 |
| rs68055295 | in-del | -/GATCAAGATGCTG | 0.384017 | 0.211044 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857508 | GGCTGGGAATGCCAA[-/GATCAAGATGCTG]GATGGTTGAGTTCTG | 5336 |
| rs68118517 | snp | C/T | 0.147321 | 0.227941 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834476 | CTGAGCCTCAGTTTC[C/T]CCTTCTGCAAAATGG | 5336 |
| rs71146046 | in-del | -/A | 0.503043 | 0.0873416 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781413 | AAAAAGAAAAAAAAA[-/A]CAGAAAACAACTGCT | 5336 |
| rs71146047 | in-del | -/AAG | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816651 | AAAAAAAAAAAAAAA[-/AAG]TTAAAATTAGCTGGG | 5336 |
| rs71146048 | in-del | -/GGAAA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824005 | GGAAAGGAAAGGAAA[-/GGAAA]AAGAAAAAGAAACAG | 5336 |
| rs71146049 | in-del | -/CAGGA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824081 | AAGGACAGGACAGGA[-/CAGGA]CAGGACAGGACAGGA | 5336 |
| rs71146050 | in-del | -/ATATAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838779 | TATATATATATATAT[-/ATATAT]TTAATTTTACTTTAA | 5336 |
| rs71146051 | in-del | -/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855208 | TTTCTTTTTCTTCTC[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs71146052 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877999 | GCGAGACTCCCTTTC[-/A]AAAAAAAAAAAAAAA | 5336 |
| rs71146053 | in-del | -/TTA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906087 | TGGTTATGTAGGATG[-/TTA]TTAATAATATTTGGA | 5336 |
| rs71146054 | in-del | -/AA | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917228 | AAAAAAAAAAAAAAA[-/AA]GGAAAGCCTGTCATT | 5336 |
| rs71146055 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942925 | CAGCCCTCCTTGTAT[-/A]AAAAAAAAAAAAAAT | 5336 |
| rs71146056 | in-del | -/CA/CACA | 0.217576 | 0.258923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951150 | GCAGGGCCCTGTCTC[-/CA/CACA]CACACACACACACAA | 5336 |
| rs71272424 | in-del | -/TTGACATGCAGATAAAAATACATGGTCCTTTTTTCTTTGATTTATTATTCCATTGCTAA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948208 | CTTGCAGAGAACAAT[lengthTooLong]TTGACATGCAGATAA | 5336 |
| rs71272425 | in-del | AATTTTTC/CATTTTTTT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888388 | CTACTAAAATACAAA[AATTTTTC/CATTTTTTT]TTTCTTTAAATCAGC | 5336 |
| rs71376314 | multinucleotide-polymorphism | CGCAGTGAGCTGAGATCAT/TGCAGTGAGCCGAGATCCC | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859596 | CCAGGAGGCGGAGCT[lengthTooLong]GCCACTGCACTCCAG | 5336 |
| rs71376315 | multinucleotide-polymorphism | CTG/GTA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855650 | CTAGGTCTTATCCCA[CTG/GTA]CACACATCTGTCTCC | 5336 |
| rs71380486 | multinucleotide-polymorphism | AT/GA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819385 | CCCTGTGAGGCGAGG[AT/GA]GCTCCTGCGAATCCC | 5336 |
| rs71380487 | multinucleotide-polymorphism | GG/TA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842194 | AGAACTCCCTACAAA[GG/TA]GAGGCTTTCTCCTCT | 5336 |
| rs71382825 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830072 | GCCTATAATCTCAGC[-/C]ACTTTGGGAGGCTGA | 5336 |
| rs71382826 | multinucleotide-polymorphism | AG/GT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866480 | CTTTCTCCCAGGATG[AG/GT]CTCCACTGGGGCACC | 5336 |
| rs71382828 | in-del | -/A | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885323 | CCACCACGCCCAGCC[-/A]CCGACTAATTTTTGT | 5336 |
| rs71382829 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885325 | ACCACGCCCAGCCCC[-/C]GACTAATTTTTGTAT | 5336 |
| rs71382830 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916826 | TATTTTTGGTAAAGG[CA/TG]GGGTTTCACCATGTT | 5336 |
| rs71382831 | in-del | -/GT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940206 | GGAGAGCTGGTGCAT[-/GT]ACAGCCTGTCGTGTA | 5336 |
| rs71388374 | snp | G/T | 0.493293 | 0.0575177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824056 | TTCCTTTCCTGTCCT[G/T]TCCTGTCCTGTCCTG | 5336 |
| rs71388375 | snp | G/T | 0.493293 | 0.0575177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824061 | TTCCTTTCCTTTCCT[G/T]TCCTTTCCTGTCCTG | 5336 |
| rs71388376 | snp | G/T | 0.493293 | 0.0575177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824066 | TTCCTTTCCTTTCCT[G/T]TCCTGTCCTGTCCTG | 5336 |
| rs71400175 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787812 | TCTGGACATTTCATA[A/G]AAATGGATCCTATGT | 5336 |
| rs71400176 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817000 | CCCATTTATTGCCCA[A/G]AAGGTGACGGGCACT | 5336 |
| rs71400177 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835744 | GCAGTGTGGAGCTTA[A/C/G]AAGTCTGAAATCAAG | 5336 |
| rs71400178 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837155 | AAAAGACAAACTAGC[A/G]AACTCAAAGAACGAG | 5336 |
| rs71400179 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844021 | TTGCTCTGTGGCCCA[A/G]GCTGGAGTGCAGTGG | 5336 |
| rs71400180 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859627 | GCGAGCTCCGCCTCC[C/T]GGGTTCATGCCATTC | 5336 |
| rs71400181 | snp | A/G | 0.115788 | 0.21092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859727 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 5336 |
| rs71400182 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866080 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGCACC | 5336 |
| rs71400183 | snp | C/T | 0.309648 | 0.24278 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907839 | GGACCAGCCAGTCCC[C/T]GGGACCTCCTTCCCA | 5336 |
| rs71400184 | snp | G/T | 0.498206 | 0.0298983 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916805 | ACCATGCCTGGCTAA[G/T]TTTTGTATTTTTGGT | 5336 |
| rs71400185 | snp | C/G | 0.159292 | 0.232964 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930852 | AAGTGAAACAGTTCA[C/G]AAAATTTTATGTATT | 5336 |
| rs71400186 | snp | G/T | 0.5 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81937787 | ATGAATCACGCATTG[G/T]TTTCTCTCAATGGGC | 5336 |
| rs71400187 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958534 | TACTTTAACTACCAC[C/T]GGCTGCCTGCTGCAG | 5336 |
| rs71695772 | in-del | -/TAAT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911598 | GCCACTGTGCCCAGC[-/TAAT]TAATTAATTAATTAA | 5336 |
| rs71712849 | in-del | -/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873554 | AGTTGCAAATAACAG[-/T]TTTTTTTTTTTTAAT | 5336 |
| rs71727409 | in-del | -/A | 0.0865458 | 0.189163 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895576 | AAAAAAAAAAAAATG[-/A]AAAAAAAAGCAGCAT | 5336 |
| rs71878326 | in-del | -/AT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900112 | GTATGCATGCACACA[-/AT]TGCAAATTACATATG | 5336 |
| rs71911955 | in-del | -/ATAC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899288 | TATATATATATATAT[-/ATAC]ACACACACACACATA | 5336 |
| rs71915851 | in-del | -/T | 0.321053 | 0.23969 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941564 | GTTTAAAGTTTCTGA[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs72528154 | in-del | -/G | | | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777658 | AGATCTTGTGAAGTC[-/G]ASAAACGAGTCCTAT | 5336 |
| rs72820808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878962 | TTGCTTCAACAAGCA[G/T]AGTGTCCGGGCAGGG | 5336 |
| rs72820812 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880292 | TGTACCCCAGTGGAG[A/G]TGCCTATCTCAACTG | 5336 |
| rs72820814 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882657 | TCTTTCTTTCCTCCC[C/T]TCCCTTCTCTTTTTT | 5336 |
| rs72820819 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895416 | TACAAAAAAATTAGC[A/C/T]GAGCGTGATGGTACG | 5336 |
| rs72820823 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897001 | GAGCCAGATACAAAT[G/T]TTTCAGGCTTTATGG | 5336 |
| rs72820826 | snp | C/T | 0.258565 | 0.249853 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898955 | TTTCGGAGGCTGAGG[C/T]GGGTGGATCAACTGA | 5336 |
| rs72823102 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907480 | AAAGAAGCTCAAATA[C/G]CAAAAGAAGCTCAAA | 5336 |
| rs72824903 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907496 | CAAAAGAAGCTCAAA[A/G]TGCATCGATATTTTA | 5336 |
| rs72824905 | snp | C/G | 0.0101012 | 0.0703459 | missense | PLCG2 | GRCh38.p7 | 16:81908423 | CGGCCCAGGATATAC[C/G]CCCTACAGAACTACA | 5336 |
| rs72824907 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909291 | CTCCCTTTATTGGGG[C/G]GGTTTAATGTGAGTT | 5336 |
| rs72824911 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914064 | AAGCCTCTTAGTGGT[A/T]CCTCCTCAGCCTGGA | 5336 |
| rs72824912 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914909 | AGTTGGGGTGTGAGG[A/G]CTGATCCTGTTGTAT | 5336 |
| rs72824913 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920153 | TAAATAAGGATGAGG[G/T]TTCACAGGTGACTTA | 5336 |
| rs72824919 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923799 | ATATTAACAGGTATC[A/G]ACATATCATATCATA | 5336 |
| rs72824930 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926848 | TCTTTGATTAAACAT[G/T]AAGATCATGTGATGG | 5336 |
| rs72824935 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940502 | ACTCCCCAAACCCTT[C/G]AGAATTCACCTTCTT | 5336 |
| rs72824936 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941704 | ACTGTAAACTCCCCC[C/T]TTTTTTTTTTTGAGA | 5336 |
| rs72824938 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942228 | CCCTCCCAGTGCCTT[C/G]CAGAGATGTCAGAGT | 5336 |
| rs72824939 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942457 | CCTGGCACATCCATA[A/T]TCATGGGAGGAATGA | 5336 |
| rs72824941 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944654 | ATTTTATTTTATTTC[C/T]TGTAGAGATGGGGGT | 5336 |
| rs72824943 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947133 | AAACAACCGGAAACA[C/T]TATAAATAATTTAAG | 5336 |
| rs72824944 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947504 | CTCCTTAATGCCCAC[A/G]GTCATACCTTTTATT | 5336 |
| rs72824945 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948419 | AAACTGGCTGCCCCA[C/T]GACCTGTTTAGTACT | 5336 |
| rs72824949 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950132 | ATTGAAGTGAAATGG[A/G]TAAGAACTTACATTT | 5336 |
| rs72829118 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953068 | ACTGCATCGCCTCAA[A/C]CAAATTATAAGAAGA | 5336 |
| rs72829120 | snp | A/C | 0.039522 | 0.134904 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958809 | CTGGGAGGCTGCTGG[A/C]ATGGCCCTTGGTCCA | 5336 |
| rs72829122 | snp | A/G | 0.0205511 | 0.0992634 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960066 | AGTCAGGGGATTATG[A/G]CATAAATGGTGCTGG | 5336 |
| rs72829125 | snp | C/G | 0.0178098 | 0.0926698 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961241 | TATCTGTGTGAACAA[C/G]GATCAACATCTCCAT | 5336 |
| rs72832034 | snp | C/T | 0.1652 | 0.235179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824643 | GGCATTCAGATTCAG[C/T]GGTTATAATTAAAGG | 5336 |
| rs72832043 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826805 | CTGGAACAGCTTTAC[C/T]GTGATTTTCTAGTAT | 5336 |
| rs72832045 | snp | A/T | 0.139564 | 0.224285 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827643 | TGCACACTGGGAAAG[A/T]TCTAAGGGTGGTGGG | 5336 |
| rs72832046 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827662 | AAGGGTGGTGGGAAC[C/T]GTGGTTAACGGGGAG | 5336 |
| rs72832048 | snp | C/G | 0.142947 | 0.22592 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829426 | TTTCACCATGTTGAC[C/G]AGGCTAGTCTCGAAC | 5336 |
| rs72832050 | snp | C/T | 0.13446 | 0.221699 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832178 | AAAGCCTTTGCTCAG[C/T]GCCTGACTCATGGTG | 5336 |
| rs72832051 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832179 | AAGCCTTTGCTCAGT[A/G]CCTGACTCATGGTGA | 5336 |
| rs72832055 | snp | A/G | 0.424193 | 0.179323 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835782 | TAGGGCAGTGCTCCC[A/G]CTGGAGGCTCTAGGG | 5336 |
| rs72832056 | snp | C/T | 0.122064 | 0.214785 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835924 | CAAATTTCCCTCTTA[C/T]AAGGACAGTAGTCTT | 5336 |
| rs72832057 | snp | C/G | 0.0441359 | 0.141981 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836087 | ACCCCCAACATTACC[C/G]GTTTATACTTTCTTT | 5336 |
| rs72832061 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843827 | GAAAGAAGAACTCAA[C/T]AGAATGGGCAGGATG | 5336 |
| rs72832062 | snp | C/T | 0.430732 | 0.172731 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843865 | TGATGTGCCGTTGGT[C/T]GTGTGTCTAACTGCT | 5336 |
| rs72832063 | snp | A/G | 0.483491 | 0.0893421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844334 | TTTCTTTCTTCTTTC[A/G]GATGGAGTTTCACTC | 5336 |
| rs72832064 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844910 | TCCTTAATGTTCACA[A/G]CAAATAAATTGAGAC | 5336 |
| rs72832066 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846781 | TTTTCAATTCACATT[C/T]AATACAGCACGAAAC | 5336 |
| rs72832068 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847454 | GGGCTGAAAGTTCCA[A/G]CCCTCTAATCACATC | 5336 |
| rs72832070 | snp | C/G | 0.404559 | 0.196498 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848622 | TCTTCCTCTCTGTCC[C/G]CTGCTCTGCTCAGTC | 5336 |
| rs72832071 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850307 | GTATTTTGGGGTGCA[A/G]CATCATGAAGTCTGT | 5336 |
| rs72832075 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851147 | CTAATAATAGGGCCA[A/C]CCATAATTGAGAAGT | 5336 |
| rs72832078 | snp | C/T | 0.464735 | 0.128019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852926 | TCCATGGCCTCTCCA[C/T]AGGGCTAACTTGGGC | 5336 |
| rs72832080 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853444 | CAGTGACCAGTTTCA[C/T]AGAAGACAGTTTTTC | 5336 |
| rs72834726 | snp | G/T | 0.320575 | 0.239832 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781191 | TAGTAACCACTCTCC[G/T]GGATTTACCAGAAGA | 5336 |
| rs72834727 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781651 | GTATTCCCTCTAATG[A/C]TGCAGGGTGGGTGTA | 5336 |
| rs72834728 | snp | A/G | 0.203267 | 0.245593 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782654 | TTAGAAGGGCATTTC[A/G]TGAGATACAAGAACC | 5336 |
| rs72834729 | snp | C/T | 0.456332 | 0.141164 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783213 | GGGAGTGGGGAACTC[C/T]AGGATGCATGGCTGG | 5336 |
| rs72834730 | snp | A/G | 0.303187 | 0.244277 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783887 | CTTAAACTTAAAGCC[A/G]GTTCCTCCTGCTTCA | 5336 |
| rs72834731 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783983 | AAGTGCCTAGCCACA[C/T]TCCAGATTAAATTTA | 5336 |
| rs72834736 | snp | C/G | 0.222035 | 0.248431 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787756 | CCCTACCAGACGTAA[C/G]CAACCGTTAAATTTA | 5336 |
| rs72834740 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794936 | GTTGACATTTTTATT[A/C]TTGATGGTGCTATAG | 5336 |
| rs72834746 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799380 | TTTTCATTTTGTACT[A/G]CTTTGTGACCATGTT | 5336 |
| rs72834748 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800881 | ATCACAAAGGTCCTT[A/G]CAGGAGGGAGGCAGG | 5336 |
| rs72834753 | snp | C/T | 0.248471 | 0.249995 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809650 | ACCAGACTTGGGCCA[C/T]CCTGGGACTTGCTGT | 5336 |
| rs72834754 | snp | C/T | 0.205052 | 0.245926 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809681 | TTTCTCTGTTCCCTG[C/T]GGTGTGTGAGCCTGT | 5336 |
| rs72834758 | snp | G/T | 0.233818 | 0.249476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813554 | AATTGCTTATCAGCT[G/T]AAGGAGATTTTTCTA | 5336 |
| rs72834769 | snp | C/G | 0.215144 | 0.247558 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823392 | AGTCCCTGAAATGCT[C/G]CTCCCCACCCCTCGC | 5336 |
| rs72837428 | snp | A/G | 0.344815 | 0.231323 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868678 | GAGTCCTGGGCAGAA[A/G]TCACATCATGTCAAC | 5336 |
| rs72837429 | snp | C/G | 0.345704 | 0.230956 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868978 | CTTATTGGGGCATCA[C/G]CCTACCCTGTGAGTC | 5336 |
| rs72837430 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870061 | CTGGAAAAATTATCC[A/C]ATTTTATTGCTTATC | 5336 |
| rs73587615 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780700 | CACTCATTGGGTAGA[A/G]TCAATGAAAAGCTGC | 5336 |
| rs73587629 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782211 | AAGCTTATGAGATAC[A/T]AGAACATGAATGAGC | 5336 |
| rs73587632 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782771 | GATTCTGTTAAAATG[A/G]GGCACAGGCAAATAC | 5336 |
| rs73587667 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786502 | GTCTGGTTCCCACAA[C/G]TGGTCGAGTCATCTT | 5336 |
| rs73587670 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787186 | AGGCTTTTGTTATTA[G/T]TCGAAGTGACTATCA | 5336 |
| rs73587671 | snp | C/G/T | 0.135825 | 0.222405 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787373 | ACCATGGGAATGCAC[C/G/T]GCCATGCCTGGATAA | 5336 |
| rs73587677 | snp | C/T | 0.104504 | 0.2033 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788081 | TGTTTTGGGTATATA[C/T]CTAGGAGTGGAATTG | 5336 |
| rs73587678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788200 | GTAGAAAAGGGTGAT[C/T]GTTGCATTATTCTTC | 5336 |
| rs73587698 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793471 | GGAATTTTAGGGTCG[A/G]CTGTGGTGATGGGCC | 5336 |
| rs73587702 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793631 | TCTCAAACATATGAG[C/T]TGTCTGTTTCCTTGG | 5336 |
| rs73589225 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801688 | TTATTTTCTTTAATT[A/T]TTTTTTTCTTGAGGT | 5336 |
| rs73589244 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810545 | ATGCCCTGCTGAGGT[C/T]AAACAAGATGACACT | 5336 |
| rs73589302 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834401 | GGCGCGGGTGGTGTT[C/G]GAGAACTCTGGGCCT | 5336 |
| rs73590818 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838017 | AGAGACTAAAGCAAT[C/G]TAATGATTTCTTACA | 5336 |
| rs73590821 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838819 | TATATGTAAATAACA[C/T]AGATGTGGTAAAATG | 5336 |
| rs73590826 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839837 | GGGAGGATCACTTGA[A/G]GCCAGGGATTTGAGA | 5336 |
| rs73590833 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840714 | GCTAGACCCCTGCTC[A/T]CCTCCTGCTGTGCGG | 5336 |
| rs73590839 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842360 | TCACATATCATATGC[C/T]GGCCTGGACAGGGCC | 5336 |
| rs73590840 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844403 | TCACTGCAACCTCTG[C/T]ACCCCCACAATGGGT | 5336 |
| rs73590842 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845262 | TATTTCTTATGCCTT[A/C]TATGTGTCCAGCTTG | 5336 |
| rs73590844 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846120 | GGAGTGTTGGGTGTC[A/G]TGGCTCACAGGTGCC | 5336 |
| rs73590847 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846552 | TTATCCTCAAGGATG[A/G]GGCTACTGTATCTGT | 5336 |
| rs73592931 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854247 | GTTTGTGGGGTGGCA[A/G]CAAATGCCCGGGTAG | 5336 |
| rs73592942 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855114 | ATTTGAAAGGCTGAG[A/G]CACAAGAATTGCTTG | 5336 |
| rs73592971 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857758 | TTCAACATATGAATT[C/T]GGAAGGAATGCAAAT | 5336 |
| rs73592975 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859356 | AGGGAGCCTCTATTC[C/T]GCAGAAAATTCAAGT | 5336 |
| rs73592978 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859939 | TCTTGGAGAAGCTCC[A/C/T]TATCAGTCCTGCACA | 5336 |
| rs73592981 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861095 | ATTTATTGAACAACC[A/G]TGTATTTGGCATGCC | 5336 |
| rs73592990 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861964 | CTGTGTGCTCACCGG[C/T]TTCCTCTCCTCTACC | 5336 |
| rs73592995 | snp | C/G | 0.204189 | 0.245767 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864423 | TGTGGCTAGCAGCTA[C/G]TACCTCAGACAGCAC | 5336 |
| rs73594809 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868108 | TCCAGGCTCTGCTGC[A/C]TGCCATCCAGCTCTA | 5336 |
| rs73594812 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868147 | GTTGTGTACCCATGT[A/G]ACACCCCACCCTTGG | 5336 |
| rs73594830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870286 | AGGAGCATAGTAGTG[A/G]TTCTCCCATTTTACA | 5336 |
| rs73594838 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871033 | ACAAGAAGTGTTGAA[C/T]CTCCATTTTAGTCAA | 5336 |
| rs73594854 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872953 | CCTGATGGGTGACCA[C/T]TGGCCGTGGGACTTT | 5336 |
| rs73594867 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874787 | GAGCTTCAGAGTTTC[C/T]AAAAGTTTGGCAGCA | 5336 |
| rs73594884 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878921 | TGCAAACACGTTCCC[A/G]GGTGCCTGTGCCAAT | 5336 |
| rs73594889 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880190 | AGGCTGTGGTGAACT[A/G]TGGTCGTGCCACTGC | 5336 |
| rs73594899 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882521 | CCAGCTCTCCCTCTA[C/T]GGGCGGGTGGTGTGT | 5336 |
| rs73596812 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886470 | CTTTACAACTCGATT[C/G]TATATCTGGAGTAAA | 5336 |
| rs73596818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886695 | GAGGCTCATGACTGG[A/G]ACCACTTACTTAATG | 5336 |
| rs73596833 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892395 | ATTTAGTCTGTCTTA[A/T]TGGGTGAGGGGTGAA | 5336 |
| rs73596847 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897340 | GAATCCAGCTGTTGA[C/G]TACTAGTTTGGGCAA | 5336 |
| rs73596852 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900086 | ACATATATACACATA[C/T]AAATAATAAATGTAT | 5336 |
| rs73596854 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900143 | TGTGCATATGAATGA[G/T]AATATATAAAACCAA | 5336 |
| rs73596857 | snp | C/G/T | 0.0883596 | 0.190715 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901541 | GGTTTCACAGACCCC[C/G/T]GAAGAATCCACGGTT | 5336 |
| rs73596860 | snp | A/G | 0.093417 | 0.194889 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903251 | CATGTACCCTATATT[A/G]TCACTGGGCCACCAA | 5336 |
| rs73596862 | snp | A/G | 0.093777 | 0.195178 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903715 | TGGTGAGTCTTCGGG[A/G]CAGCCTGGTTGCATG | 5336 |
| rs73596863 | snp | C/T | 0.093777 | 0.195178 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903733 | GCCTGGTTGCATGTG[C/T]TCTTCCCTGTTCCCA | 5336 |
| rs73596864 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903760 | CCCAGCTCATTCCTT[C/T]TGTTTCCATTAGGAT | 5336 |
| rs73596869 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905570 | GCTGCTTCTTGGAGC[A/C]CTGCTGGGAGCTCTG | 5336 |
| rs73596870 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908706 | GGGACCTGAATCCCA[G/T]GCTTCATTTGTCTAG | 5336 |
| rs73596878 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910235 | AGCTGGGATTACAGG[C/G]ATGCACCACCATGCC | 5336 |
| rs73596885 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919200 | TTCCCTAGGAAGCTC[C/T]TAAAGTCAAGTCCTG | 5336 |
| rs73596897 | snp | G/T | 0.102726 | 0.202016 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929331 | CTCCCCTAGGACTCA[G/T]GTGACAGCAGCCCCA | 5336 |
| rs73598703 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932147 | AGTGACCTTTTCAGG[A/G]CTGTCCTACCTGAAG | 5336 |
| rs73598704 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932170 | ACCTGAAGTACTAGT[C/T]TCTGGCTGGAAGTGT | 5336 |
| rs73598705 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932347 | TCCTAACTCACAAGT[A/G]CTTAATCACTGCCTT | 5336 |
| rs73598707 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934158 | ACAGAGAAGAGCCCC[C/T]TTCCATCCTGACCTC | 5336 |
| rs73598710 | snp | A/G | 0.000399281 | 0.0141238 | missense | PLCG2 | GRCh38.p7 | 16:81934489 | GAGCTCTCTGACCTG[A/G]TTGTCTACTGCAAAC | 5336 |
| rs73598727 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947205 | AAAGAAAATTGTGTT[C/G]ATGCAGATTTGACTT | 5336 |
| rs73598737 | snp | A/G | 0.0726307 | 0.176182 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959076 | TGTTAATACATACCA[A/G]TAATGTAATATGGCT | 5336 |
| rs73598741 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961421 | ATAATTTAGTGAAAT[C/T]TGGGCTATGTGTTTA | 5336 |
| rs74029214 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795038 | CAACCTTAGAATGTT[A/C]TTAGAATTTGTTCCT | 5336 |
| rs74029218 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801538 | CCTGTCAATGCTGGA[C/G]ATTTAGGTTGTTTCC | 5336 |
| rs74029219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801568 | CAATCATGATACTCC[C/T]GATTCCAGCAAACAC | 5336 |
| rs74029220 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810487 | TTCTGTGGTCATTCT[A/T]GGTGATGCAGACTGG | 5336 |
| rs74029223 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814863 | GATTATGATGATCCT[C/G]TCCCCATAGAGTTGG | 5336 |
| rs74029224 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814886 | AGAGTTGGGATAAAG[A/G]TTAAATGAGCCAATA | 5336 |
| rs74029225 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815769 | GCGCTATAATTGAGC[A/G]GTCTTAAATGACCAG | 5336 |
| rs74029227 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819462 | CCCAGGAAGCCTGAG[A/G]CTTAGCTGGGTGGAC | 5336 |
| rs74029228 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821820 | AGGTTTTACTGCAAA[C/G]AACTTTTGGGGACCC | 5336 |
| rs74029229 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821929 | GGCCTGGGGTTCCAT[A/C]CCAGATCCACCATTT | 5336 |
| rs74029234 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831480 | TCATGTCAATGCCAC[A/G]AAACTGGCCCTCTCT | 5336 |
| rs74029235 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833992 | ACCCCAAGGTTTTCT[A/G]AGAGGTCATTCAGGG | 5336 |
| rs74029236 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834240 | TCAACTCTGACACCT[A/G]TTAAATGTTCAGTAA | 5336 |
| rs74029237 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834474 | GCCTGAGCCTCAGTT[A/T]CCCCTTCTGCAAAAT | 5336 |
| rs74029238 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835010 | CATTGCCCACCTCCT[A/G]GTGTCATGAACACTG | 5336 |
| rs74029239 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837521 | CCTGGGAGGAGTAAG[G/T]GATGCTCTCCGCAGG | 5336 |
| rs74029240 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838853 | ACATGGTGCATGTAA[C/G]GCTCAAGGCTTTAAG | 5336 |
| rs74029241 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839237 | ATCACATAAATAGTA[A/T]CAGCAGTAGGCAGAT | 5336 |
| rs74029242 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840356 | GAAGATAACTTTTCC[A/G]TGGGCCAGATTGGCC | 5336 |
| rs74029244 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840675 | GATGATCTGACAGGA[A/G]GTGGAGCTCAGGCAG | 5336 |
| rs74029245 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840753 | CTAACGGGCCACAGA[C/T]AGGTGCCAGTTCATG | 5336 |
| rs74029246 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840949 | TGGGGAGTCCCAGAG[C/G]GGAGAGAAGCACCAG | 5336 |
| rs74029247 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841121 | CTGCTGTCAGCGCAG[C/T]GGCAACAACTCTGTT | 5336 |
| rs74029248 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842027 | GTGATTTTTATTTCA[C/T]GTTATTTCATTTGGT | 5336 |
| rs74029249 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842498 | GAATAACTGAAAGTC[A/G]GAAAAGAGGTTGGGG | 5336 |
| rs74029250 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843166 | GTCTGCTGACCACAG[C/G]CTACTTTGAGAATAA | 5336 |
| rs74029251 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843316 | GTGGAAATCTTTTGG[C/T]ACCCTTTCTCACACC | 5336 |
| rs74029252 | snp | A/G | 0.211212 | 0.246973 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843560 | CTACCAATATTTTTC[A/G]CGTGAATACAAAGCA | 5336 |
| rs74029254 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846740 | CAATCCCAACCAAAA[A/T]CTAATAGAGATACAA | 5336 |
| rs74029255 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846907 | ATGGTTTTCCCCCCA[C/T]GCATCAAGCAAACAA | 5336 |
| rs74029257 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847316 | CAACCAAGAAGCTCT[C/G]TAAGCCCTGTCATCC | 5336 |
| rs74029258 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850679 | GGGCTAAAGTAGGCA[A/G]GGAGTGATATTTAAG | 5336 |
| rs74029284 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864029 | GGGCATGGCCTCTGG[C/T]GTTGCAAATTTTTTA | 5336 |
| rs74029289 | snp | C/T | 0.290201 | 0.246747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874717 | CCAAATGGTTTCCAT[C/T]GTGAGCTTGCTAGTT | 5336 |
| rs74029293 | snp | C/T | 0.362523 | 0.223246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879832 | CTCCATGGCGCCCCC[C/T]TTGGTGGAAGAGCCT | 5336 |
| rs74029298 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900512 | CCCCCGAGCAGCGCC[C/T]GGTTTCTGTCGTCCC | 5336 |
| rs74029299 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903677 | TCGGCCATGGAGGGT[C/T]CATGGCTTCTCAGGC | 5336 |
| rs74029301 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903804 | TTCCCAGGGAGTTTT[C/T]AGCTCTTGTTCTAAG | 5336 |
| rs74029302 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904228 | CTTTCACGTTCTTTG[A/C]CTTACGGGATCCCAC | 5336 |
| rs74029303 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922904 | GTGAACAGAGACCAC[C/T]TTTTGATGAATTTCA | 5336 |
| rs74029304 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923099 | TGACAGTCTTGGCTT[A/C]ATCTAAAAGGCATGT | 5336 |
| rs74029305 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926395 | TTGCATGTCTGGGCA[C/T]GGCCTTGCCGGGAGG | 5336 |
| rs74029306 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932459 | AACTGGAAAGAAATT[G/T]TAGGGTTTCCCATGC | 5336 |
| rs74029307 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940161 | TTTTTCCTGGTTTGG[A/T]TGGAATCACTGTAAA | 5336 |
| rs74029308 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941420 | AGGAATCTGCATCTT[A/T]AGGCAGCTCCCCAGA | 5336 |
| rs74029309 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942116 | ACTGCCTGCCAGTTC[C/G]TCTACTGAACTCATC | 5336 |
| rs74029310 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942921 | AGAAAAACAATTATT[A/T]TTTTTTTTTTTATAC | 5336 |
| rs74029311 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943128 | ATAGCCTCCCGGAAT[A/G]CCATGGAGCAAACAG | 5336 |
| rs74029312 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943178 | CAGTCAATCAGCAGC[C/T]AGACTGTATTAGTCC | 5336 |
| rs74029313 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945742 | AAAGATTTCCTCCCA[C/T]TGGAAATCTTTAAAG | 5336 |
| rs74029314 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947023 | TACATAAAACCCCTC[A/C]GCAGACACTTCACAG | 5336 |
| rs74029317 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953264 | AGACTGGTGGAAAAC[C/T]CAGTGAAATATGAAT | 5336 |
| rs74029318 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962241 | AAGGACCTCAACCCT[G/T]TTGACTTTAAAAGGA | 5336 |
| rs74032904 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905566 | TGCAGCTGCTTCTTG[A/G]AGCCCTGCTGGGAGC | 5336 |
| rs74032905 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906219 | TTTCCTGTTTCAGGA[C/T]CCAGTACCCGGTGCT | 5336 |
| rs74032908 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912881 | GCTGCGAGAATGTGC[A/G]CTCCTGCGTGCCAGG | 5336 |
| rs74032910 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914059 | CCCCTAAGCCTCTTA[C/G]TGGTACCTCCTCAGC | 5336 |
| rs74032922 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914240 | CAAGCGGTGAGACAG[C/T]TCTGACACAACCGGA | 5336 |
| rs74032923 | snp | C/T | 0.00476369 | 0.0485711 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81921224 | AAACTCCCTCTACGA[C/T]GTCAGCAGAATGTAT | 5336 |
| rs74032924 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921617 | GGTTCACTGACCTCC[C/T]TGCAGTGCAAATGCT | 5336 |
| rs74032925 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921747 | AATTTAGTTTGAGCC[A/G]GCAGAGGAAGAACCA | 5336 |
| rs74032926 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921986 | AGAGACCTTAGTAGC[A/G]AAAACTTTTGTTAGT | 5336 |
| rs74248288 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824425 | AAGCGTGAGCCACTG[A/C]ACATGGCCCCAGCCA | 5336 |
| rs74248292 | snp | A/G | 0.462034 | 0.132445 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852792 | TTGTCTGTGTTCCAC[A/G]TGTTGTCAGCTGGGG | 5336 |
| rs74264894 | in-del | -/TTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893976 | CTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCCCTG | 5336 |
| rs74331168 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932150 | GACCTTTTCAGGGCT[C/G]TCCTACCTGAAGTAC | 5336 |
| rs74348074 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804376 | ACAGTGTCCTATTTT[C/T]AACTTTTCTGGGCCC | 5336 |
| rs74369165 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904897 | ATTTTTACTTATTTA[G/T]TTTTTACTGGGACAG | 5336 |
| rs74383491 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835844 | GGTAGCTGCTGGTGA[C/T]CCTGGGTGTCCCTTG | 5336 |
| rs74398663 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909920 | GGTGACCTGCTCCAG[A/G]ACACTTGGTTCATAT | 5336 |
| rs74448193 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891946 | GACTCATTGAATTGA[C/G]TTATAGGGAGTGTGT | 5336 |
| rs74451556 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859522 | TTGATTGACCGTGAA[A/G]AAGTAAACCAGGTGG | 5336 |
| rs74470864 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804984 | CATTACAATCTGTCT[C/G]TGAGTTTTGCCTGGT | 5336 |
| rs74515934 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859614 | ATCTCAGCTCACTGC[A/G]AGCTCCGCCTCCTGG | 5336 |
| rs74523236 | snp | A/G | 0.226779 | 0.248919 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793946 | TTGTTTTCTTCTCCT[A/G]AATGATCTCAAAGAC | 5336 |
| rs74543284 | snp | C/T | 0.128632 | 0.218563 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845608 | CATGAATTTGCAGCC[C/T]CTGCACTAGAATCTT | 5336 |
| rs74581105 | in-del | -/AA | | | splice-acceptor-variant | PLCG2 | GRCh38.p7 | 16:81893707 | GCCTTCTCTCCTGCA[-/AA]GGTACCTTACAGGTG | 5336 |
| rs74599228 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787219 | GTACTCTTTTTTTTT[A/T]AAAACAAAATTAATT | 5336 |
| rs74604180 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799293 | TCCAAATCTTTTTGT[C/G]CAACAAAACTTTATT | 5336 |
| rs74649627 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942484 | ATGAAATAGAATGAA[C/G]AGGAGGCATTGAGGG | 5336 |
| rs74651519 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940236 | GCACACAGGTGGGAG[C/G]AAGTGGGTGACAGGG | 5336 |
| rs74665088 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908970 | GATTCAGCCAACCTT[C/G]TAGCATCTCTGTCTC | 5336 |
| rs74675064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878581 | CCAAGAGCTGTCTAC[A/G]CTTCCCTTCTTCCTA | 5336 |
| rs74710389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837812 | TGTGAACGTTACCCA[A/G]TTATCCCCAATGGTA | 5336 |
| rs74714753 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892652 | TAAGAAATACAAACT[A/T]AAAAAAAAAACTTTT | 5336 |
| rs74715887 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857770 | ATTCGGAAGGAATGC[A/G]AATATTCAGTCTGTA | 5336 |
| rs74716750 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828867 | TTCTTTTCTGAATGC[C/T]GAGGTGGGTGGATCA | 5336 |
| rs74736661 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878787 | CTTGCCTTTGGGATG[C/T]CCGACTGTCTTCCTT | 5336 |
| rs74742890 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781750 | ATTTTAACACAATTG[G/T]CTTGTGGGATTTTTG | 5336 |
| rs74758109 | snp | C/T | 0.12932 | 0.218944 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849155 | ACAGCAATGGGACGT[C/T]ACGGGAAGGCTTGAT | 5336 |
| rs74763890 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926096 | TAAATTAGTGGGGGG[A/G]AGTTGGGTACCAAGG | 5336 |
| rs74809327 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814280 | AAGGTCTTCTCAGGG[G/T]ACCTGCCTGTTTTAG | 5336 |
| rs74821347 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869905 | TTTGCTTACAGGGAA[A/G]TACTCATTCTTCTTA | 5336 |
| rs74825159 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907056 | AAAAAAAAAAAAAAA[A/C]AGTGCAGCACACCAA | 5336 |
| rs74835056 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955102 | CCTCACTTGATACAT[A/T]CACTTAATCACCAAG | 5336 |
| rs74838290 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898857 | GCCTTATTTCAGATG[A/G]TTCAGGAGGAAACGT | 5336 |
| rs74856898 | snp | C/T | 0.00503917 | 0.0499419 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946172 | CTCCTTGTTCTGCTT[C/T]AGGATTCAGGTCCGT | 5336 |
| rs74884412 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856621 | TTTTATTAGTTAGCA[C/T]AGGGTTAAAAGCTAA | 5336 |
| rs74923230 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866978 | AGCCAGCCCCAGCTG[A/G]CCCAACAGGGACTTT | 5336 |
| rs74923232 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806346 | CTGTGTGTGTGATCA[C/G]GTAGCTTTAATTTCC | 5336 |
| rs74943801 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879436 | CGGCTCTTAACCTTT[C/T]GGTGGGACCTACTCC | 5336 |
| rs74945536 | snp | C/G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805519 | TTCTTTTCTTTTCTT[C/G/T]TTTTTTTTTTTTTTT | 5336 |
| rs74956269 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904496 | TGCAGCCACTTGCCC[C/G]GGGTCACACAGCTGG | 5336 |
| rs74972922 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872977 | GGACTTTGGATGTAT[C/T]TGAGTTAGAGAAATG | 5336 |
| rs74985032 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899579 | CTTCCTGGTCTACAG[C/T]GTGAAAGCTTCAACA | 5336 |
| rs74993072 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847156 | CTAGAATGGCTGACA[C/T]AACTAAGGGAAACAT | 5336 |
| rs75004072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796996 | ACTGATACTATGGAT[C/G]GGTTGTGGTTTGTCA | 5336 |
| rs75080768 | snp | A/G | 0.0198006 | 0.0977527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853570 | GGATCCCTCGCATGC[A/G]TAGTTCACCGTAGGG | 5336 |
| rs75096997 | snp | C/G | 0.148996 | 0.228688 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806202 | ACATGTGGCTAGTGG[C/G]TACCATATTGGATAG | 5336 |
| rs75109132 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900208 | TAAAGTAGGTGGATG[C/T]ACACGTGGAACAGCG | 5336 |
| rs75130618 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918908 | TGTTTCTTTTTTTTT[-/TT]AAAAAAAGTCACTGT | 5336 |
| rs75139989 | snp | A/G | 0.248188 | 0.249993 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808260 | CAACGGGGCTACACT[A/G]TTTTGCATTTGCCAA | 5336 |
| rs75151045 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892863 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 5336 |
| rs75155139 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896977 | AGGTCAACGAAATTG[G/T]TCTATAAAGAGCCAG | 5336 |
| rs75187435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834483 | TCAGTTTCCCCTTCT[A/G]CAAAATGGAGTTGAT | 5336 |
| rs75215849 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837043 | GAAGACTCAACATCA[C/G]TTACAACTCTAGAAT | 5336 |
| rs75246608 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957529 | CCAGCGGCTCTAGAC[A/T]GGGTCAAGATCCCCC | 5336 |
| rs75259348 | snp | A/C | 0.182296 | 0.240658 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789840 | TCCTTCCCTTCCCAC[A/C]TTTGCCCCCCCTCCA | 5336 |
| rs75264518 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960257 | ACATGGTATGATGGC[C/T]CTTCCCAGAGTCTAT | 5336 |
| rs75265227 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825376 | TCACTGCAACCTCTG[C/T]CTCCTGGATTCAAGC | 5336 |
| rs75280529 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819127 | TCCACATTCTGGTCG[G/T]CCTGACTGTGGGGTT | 5336 |
| rs75286934 | snp | A/T | 0.209693 | 0.246729 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793860 | GACATGCCCAAGTTA[A/T]GGAAAGGGCAGAGCT | 5336 |
| rs75304259 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918899 | TGAAAGACTTGTTTC[C/T]TTTTTTTTTTAAAAA | 5336 |
| rs75306178 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866133 | TCCCTTGCTCCCAGG[G/T]TGAGCTCCAACTGGG | 5336 |
| rs75307654 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834016 | TTCAGGGAGCAGCTG[A/C]TGGAACGTGGGAATG | 5336 |
| rs75313549 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778064 | AAAAAACAAAAAAAA[A/C]CAAAAACACACACAC | 5336 |
| rs75321352 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882245 | GCCCAGTGAGGCCCT[C/G]TTTTTCTGGTGGCCT | 5336 |
| rs75336624 | snp | C/T | 0.046775 | 0.145601 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867294 | CTCTCTTGACCACTC[C/T]GTCTCAGCTCTGCTG | 5336 |
| rs75354947 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936610 | GATTGTAAGTAAGTG[A/G]CAGAGGCTGAGTTAG | 5336 |
| rs75367728 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929669 | CCAAAGTGCTGGGAT[G/T]ACAGGCATGTGCCAC | 5336 |
| rs75373243 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781280 | CTATTTTTTTATTGA[C/G]CTCACAAATCTTTCC | 5336 |
| rs75381320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818331 | GGGAGCATTGTCATA[C/T]GGTGGTTATTTATAT | 5336 |
| rs75387007 | snp | A/C/G/T | 0.000235657 | 0.0108528 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938779 | CCCAGGGGGGTTCCA[A/C/G/T]TGCTTCCCTTTGGTG | 5336 |
| rs75392081 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821408 | TGAGTGAATGAATGA[A/G]ATAATACAAATGTAC | 5336 |
| rs75400682 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908986 | TAGCATCTCTGTCTC[C/T]TCCATAAAACGAGGA | 5336 |
| rs75401901 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929841 | GAGGTCCTTTGGGCA[C/G]GGGGGTGCAGGATCC | 5336 |
| rs75446520 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943980 | CCCATGGGCTCATTT[C/T]GAAGAGAACAAAAGA | 5336 |
| rs75450273 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870508 | ATGTCTCTTGGAAAC[C/T]TGGCTGAGACTCTTC | 5336 |
| rs75452105 | snp | A/C | 0.424503 | 0.179021 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778003 | GCCTGGGCAAGAGAG[A/C]AAGACTTTGTCTCAA | 5336 |
| rs75472227 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909571 | ACAGGCACATGCCAC[A/G]ACACCTGAATAACTT | 5336 |
| rs75472618 | snp | A/G | 0.0130316 | 0.0796616 | missense | PLCG2 | GRCh38.p7 | 16:81908570 | GCGAGACCTTCCCCA[A/G]TGACTACACCCTGTC | 5336 |
| rs75475854 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876475 | TCCTTTCCCTCCCTT[C/T]CTTAGTGCCCTGGCC | 5336 |
| rs75476465 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943707 | GTTGGCATATCACTG[A/G]GCTAGTCTGCAAGAA | 5336 |
| rs75476886 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925473 | GGCGTGAAAAGGGCT[C/T]ACAACCCGCAGTCCT | 5336 |
| rs75478380 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931287 | CCTGACACATCTTTT[C/T]GGAGGACCCTACTGA | 5336 |
| rs75479995 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955295 | CGTGTTTTTCTAAAA[G/T]TAAATGACAAAGGAT | 5336 |
| rs75511292 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931120 | TGTTTTTTTTTCCTG[C/T]ATCTTAAGTGTCCCT | 5336 |
| rs75520589 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906080 | AAGCTTCTCCAAATA[A/T]TATTAWTAACATCCT | 5336 |
| rs75529606 | snp | C/T | 0.082636 | 0.185713 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836018 | CCAAAGAAGGCCACA[C/T]TCACACATACCAGGG | 5336 |
| rs75545570 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795669 | CTATGGGCCATACCT[C/G]AAGTGGATGTACCTG | 5336 |
| rs75568981 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938709 | CTGGCATTGAACTCA[G/T]CCAGTGTCACTCTAG | 5336 |
| rs75575323 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933906 | GGAGGTACCTCCTGA[A/G]TCCATGGCACATGGC | 5336 |
| rs75601191 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845583 | TCATGACTTGGATAG[C/T]TCCTGGGAACATGAA | 5336 |
| rs75618523 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896986 | AAATTGTTCTATAAA[C/G]AGCCAGATACAAATG | 5336 |
| rs75625823 | snp | C/T | 0.142947 | 0.22592 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941585 | TTTTTTTTTGTACTC[C/T]AGAAATGTTCATTTT | 5336 |
| rs75646959 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796915 | CCTAACACACAAATA[C/T]ACTCTCATGTAACAG | 5336 |
| rs75666869 | in-del | -/TTTGT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951492 | GTTTTATAGCTTAGT[-/TTTGT]CTTCATTTAAATAAC | 5336 |
| rs75687983 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944304 | TGGGTTGAAAATATT[G/T]TTGAAAACATTATGT | 5336 |
| rs75693543 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821255 | ACATGTGAGTGATTA[C/G]AATAATGCCTGGCAC | 5336 |
| rs75693931 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777660 | GATCTTGTGAAGTCA[C/G]AAACGAGTCCTATGG | 5336 |
| rs75715894 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925885 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 5336 |
| rs75731203 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901247 | GCGGGCAGTTGCTAG[A/G]AAAGGCTGAGTGCAG | 5336 |
| rs75763423 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833616 | CTCACTGTACCTTCC[A/G]CCTCCTAGGATCAAG | 5336 |
| rs75801651 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876458 | ACGTGGGAAAACTCC[A/G]TTCCTTTCCCTCCCT | 5336 |
| rs75826294 | snp | A/T | 0.193028 | 0.243422 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806520 | TGGGGGTTGCTTTTG[A/T]CCCAGGCAGCACTGC | 5336 |
| rs75827500 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865999 | GCGTGAGAGGACGCT[A/G]GCCTCTCCCTTTCTC | 5336 |
| rs75829281 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795326 | CTCTCTGTAGAGGTG[A/T]TGTTTGAGCTGAGAC | 5336 |
| rs75846438 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907038 | ACAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 5336 |
| rs75875467 | in-del | -/AT | 0.29198 | 0.24645 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900111 | TGTATGCATGCACAC[-/AT]ATGCAAATTACATAT | 5336 |
| rs75878012 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814708 | TCAAAAGAAAAAAAA[-/AA]GACACCCTGGGGGAC | 5336 |
| rs75885992 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907036 | AGACAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 5336 |
| rs75916817 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925474 | GCGTGAAAAGGGCTT[A/T]CAACCCGCAGTCCTG | 5336 |
| rs75926723 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897972 | ATGAAGGCATATGAT[G/T]TCTCCATCGCAGCAT | 5336 |
| rs75935378 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939368 | AAGCCAGGAGGGAAC[C/T]GTGATTGGTGGGCCT | 5336 |
| rs75940041 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817878 | AAGCTCCCTGTGCTT[A/T]TGAACATGTTCTCAC | 5336 |
| rs75953259 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864359 | AAATGAAATAAAATA[C/G]TTAGCTCCTCAGTGG | 5336 |
| rs75974331 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805795 | TTTGTTTTTTTTTTT[G/T]TTTGCTGTTATTGTT | 5336 |
| rs75975000 | snp | C/G | 0.116838 | 0.211584 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952939 | CCCTGCAGCTACCAT[C/G]TTAATCAGATGATCA | 5336 |
| rs75976328 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854130 | GTCTGTGCTTATTTC[C/T]TGAAATCTCAGTTGC | 5336 |
| rs75984560 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874368 | TCTCCACTGTTTGAG[A/G]GTATAACTCTCCAGT | 5336 |
| rs75994869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801569 | AATCATGATACTCCC[C/G]ATTCCAGCAAACACG | 5336 |
| rs76003323 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821247 | GTGAGTTAACATGTG[A/G/T]GTGATTAGAATAATG | 5336 |
| rs76013251 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827190 | ATAGAGGATTGCTGG[G/T]TTTTTTTTTTTTTGG | 5336 |
| rs76081754 | snp | A/C | 0.199254 | 0.244796 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793641 | ATGAGCTGTCTGTTT[A/C]CTTGGTATTAGGTTC | 5336 |
| rs76089081 | snp | C/G/T | 1.79574e-05 | 0.00299639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938787 | GGTTCCAATGCTTCC[C/G/T]TTTGGTGTCCCAGGT | 5336 |
| rs76109083 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875432 | GGATTTGATTTTCTG[C/T]CCAACTTTGACGCAT | 5336 |
| rs76185153 | snp | C/G | 0.0189856 | 0.0955633 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960452 | TCACCATTTTCCTAA[C/G]TGTGTTATTTAGAAT | 5336 |
| rs76199444 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817097 | GCTGGTGGGGAGAGA[C/T]GGATGGTAAACAGGG | 5336 |
| rs76230660 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871823 | TTGCAGCATTACTTA[A/T]GCTGGCAAAGTACCT | 5336 |
| rs76248538 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800370 | CTCCTCCATCCTTAC[C/G]CTGCTCCCCAACAGG | 5336 |
| rs76250136 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952924 | TTTACAGCGGATAGA[A/C]CCTGCAGCTACCATC | 5336 |
| rs76262172 | snp | C/T | 0.162253 | 0.234095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781731 | AAGTATTTGCCTGTG[C/T]TCCATTTTAACACAA | 5336 |
| rs76266568 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948558 | TTAAGGCTTATCCTA[C/G]AGCAGATGCTTGAAT | 5336 |
| rs76297459 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806344 | CCCTGTGTGTGTGAT[C/G]AGGTAGCTTTAATTT | 5336 |
| rs76298128 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909433 | GTCACTTAAAAAAAA[A/T]TTGTGATAGGGTCTT | 5336 |
| rs76305111 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954870 | AAATACCATTTGACC[C/G]AGCAATCCCATTGCT | 5336 |
| rs76319709 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929249 | GCAGCTCCCATGTGA[A/G]GGGACTCTGTAGCGG | 5336 |
| rs76407063 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789202 | CTCATTGTGATGGGC[A/G]TGAGACAGGATTTTG | 5336 |
| rs76424446 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826596 | GGTTGTTGGAGGAAG[C/G]TTCTCTACAATACTC | 5336 |
| rs76451538 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942919 | GAAGAAAAACAATTA[-/T]TTTTTTTTTTTTTAT | 5336 |
| rs76466892 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904493 | AAGTGCAGCCACTTG[A/C]CCGGGGTCACACAGC | 5336 |
| rs76468473 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865995 | ACCAGCGTGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs76469788 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881057 | TGTGCAGGCGCTGAC[C/T]TCCAAAGGGGCAGGG | 5336 |
| rs76486161 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846522 | TGTAAGAGTTTTGCT[A/G]TATAGCATTTATTTT | 5336 |
| rs76503966 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801686 | TTTTATTTTCTTTAA[A/T]TTTTTTTTTCTTGAG | 5336 |
| rs76506409 | snp | A/C | 0.00495133 | 0.0495091 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956850 | TAATGAGAACCAGCT[A/C]CAGCTGTACCAGGAG | 5336 |
| rs76520449 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800087 | GGATAATAATGGTAC[C/T]TATTACACTGGACTC | 5336 |
| rs76527541 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926006 | AGGATGCCAGGGGAC[A/C]ACAGAGGAAGAGTGC | 5336 |
| rs76557492 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858870 | CTTTTTGGGGATTAA[A/T]TGACTATCATCAGAA | 5336 |
| rs76557652 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920761 | AGCGGGGTAGGGGGA[A/G]GGCACTGGTTTGTAG | 5336 |
| rs76574841 | snp | A/G | 0.095934 | 0.196885 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826445 | TGTGACCTTGAGGTC[A/G]AAGTGCTCGACCTCG | 5336 |
| rs76593045 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891398 | TTCCCCCCTGGTGGG[C/T]GCAGACCAGAAACAA | 5336 |
| rs76594819 | snp | C/G | 0.0260105 | 0.111035 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778650 | GCACTATGTTGATCA[C/G]GTTTTACAGATGGGG | 5336 |
| rs76616385 | snp | A/G | 0.441295 | 0.160954 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916827 | ATTTTTGGTAAAGGT[A/G]GGGTTTCACCATGTT | 5336 |
| rs76637735 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781423 | TTTCTGTTTTTTTTT[C/T]TTTTTTTGTATTTCT | 5336 |
| rs76646806 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952637 | AATGATAATATCAGA[A/G/T]TCTAGCACACAGAAT | 5336 |
| rs76653789 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825222 | GTGATGCTTATTTGG[A/G]AGTGTGTTTTTTTCC | 5336 |
| rs76666329 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916645 | AAGAATACAGGACAT[A/G]TTTTTTTTTTGAAAT | 5336 |
| rs76668053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902291 | TTCAGTCTGTTCCTG[A/C]AGCTATCACAAAATA | 5336 |
| rs76684441 | snp | C/T | 0.089084 | 0.191327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842425 | CAGGACTGTGTCTGT[C/T]TCTGCAGTGTGGCAT | 5336 |
| rs76704368 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798849 | AGGACTTCAGGGATC[C/G]CACTGCGTCTTCTCT | 5336 |
| rs76706042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785826 | GCCACTAGAACCTTC[C/T]CCTAAAACTCATCCT | 5336 |
| rs76733559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868431 | GCATCCCTCTTGTCT[C/T]TTCACAGTGTCAGAC | 5336 |
| rs76743224 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957594 | AATGGGGTGCGGGGC[A/G]GCCGGGGTTGCCAAG | 5336 |
| rs76760895 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906864 | CTAACATGGCGAATC[A/C]CCGTCTCTATTAAAA | 5336 |
| rs76782102 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805805 | TTTTTTTTTGCTGTT[A/G]TTGTTGTTTTGTTTT | 5336 |
| rs76789431 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920659 | CTAAGGTGACATGAG[A/G]AACAGAAAGAAGAGT | 5336 |
| rs76790324 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894205 | AGGCTGAAGTGGGAG[C/G]ATTGTATGAGGCCAA | 5336 |
| rs76797987 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923349 | ATGCCAGTCCCTCTC[C/T]AGCAGATGACTTTGT | 5336 |
| rs76798124 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810894 | TGACTATATTTATAA[C/T]GAAAATGAAGGTAAC | 5336 |
| rs76813563 | in-del | -/TTACT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818906 | TTTTTTTTTTTTTTT[-/TTACT]GTGGTGGGGCTCTTT | 5336 |
| rs76829509 | snp | G/T | 0.181659 | 0.240478 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859597 | TGGAGTGCAGTGGCA[G/T]GATCTCAGCTCACTG | 5336 |
| rs76862568 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896627 | AAAAAGTGAGGCAAG[G/T]AAAGTAAAATTCCCC | 5336 |
| rs76863303 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835597 | TATAATAATAATAAT[A/C]ATCATAATAATAATG | 5336 |
| rs76870294 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847429 | CTCTCCTTCCTGGAC[A/G]TTGGGGGTAGGGCTG | 5336 |
| rs76883178 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879717 | AGACTGTTGAAGCAA[C/G]GCTACCTGGGCAGAA | 5336 |
| rs76895409 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789708 | TATTATAATAAGTCC[C/T]CCGGATGGTCTGGTA | 5336 |
| rs76902880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825137 | TTTTGGAAATCAGAC[C/T]TGCATAATTGCAAGA | 5336 |
| rs76917103 | snp | A/T | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857032 | ATCTCATGCAACCAG[A/T]CTATTTTAGACTTCT | 5336 |
| rs76922088 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924560 | TGAGATTTGAACCGC[C/T]AGGCCTTTTGACTCC | 5336 |
| rs76930182 | snp | A/C | 0.0170346 | 0.090782 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933456 | GGCAGAGGGCAGTCA[A/C]AAAATCCTTCTAGTT | 5336 |
| rs76953434 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795084 | ATACTCAAAGAGGAC[C/G]TGATGTGTGTTGGGC | 5336 |
| rs76958413 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939263 | GGGTGAACCTACGTG[A/G]CTGACCTGACCCAGA | 5336 |
| rs76995312 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891288 | ATGGAACAAATATGT[A/C]GCTGCAGCCCATTGC | 5336 |
| rs77002365 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848602 | CTTGTCTCCTCCTCT[G/T]TCCTTCTTCCTCTCT | 5336 |
| rs77017238 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845264 | TTTCTTATGCCTTAT[A/T]TGTGTCCAGCTTGAT | 5336 |
| rs77033577 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843286 | TCACTAGTAGTGCCT[A/G]TTGTCAGCAAGTTGG | 5336 |
| rs77055354 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962344 | CAAAAAGTTAATAAT[C/T]AGATTTGGAATTATA | 5336 |
| rs77055788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943769 | TAGCAACAAAAATCA[C/T]ATTGTAGCGATAGGG | 5336 |
| rs77062744 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957715 | TTACTCACATTATTC[C/T]CATTGAATCTTCATG | 5336 |
| rs77062887 | in-del | -/C | 0.34526 | 0.23114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869125 | CTCTCTCATAGAGGG[-/C]TGCCTGAGGTGGGAA | 5336 |
| rs77096052 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794581 | GACCTTGGGTCTCTC[A/C]TGTCACCTCTTTGGG | 5336 |
| rs77109591 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941757 | GGCTGGAGTGCAGTG[C/G/T]GTGATCTCGGCTCAC | 5336 |
| rs77119175 | snp | C/T | 0.117537 | 0.212022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803510 | TTACTGTTTTCATTT[C/T]CTTTGTTCTTTCTTT | 5336 |
| rs77137814 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804559 | ACTTCTGCTTTTTTT[G/T]TGGCACAAAAGGACC | 5336 |
| rs77145154 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784377 | TGTCTTCCCAGCTGC[C/T]CCTTGTGGGCATTTA | 5336 |
| rs77146682 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840638 | AATAAGGTTTGTGCT[C/G]CCATGAGAATCTAAC | 5336 |
| rs77149853 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942985 | TGGGCAGCGAGAGAA[C/G]GTACATAGAGCTGGA | 5336 |
| rs77153917 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893908 | TGGACACATAATAAC[C/T]GTGCATATTTATGGA | 5336 |
| rs77170887 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858571 | GTTTTCAGCGTTGGC[C/G]TATTGGAGTGAGTGG | 5336 |
| rs77201374 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906769 | GTTGGGCCAGGCGCG[A/G]TGGCTCATGCCTATA | 5336 |
| rs77214275 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780203 | CAGGTGGCCTTGCCC[A/G]TCGGAACTTAATTTG | 5336 |
| rs77236903 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845967 | CTCCACATCTCAGTT[C/T]CCTCATTTGTAAAAT | 5336 |
| rs77236912 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952148 | AGAAAAAAACATAAA[A/G]TCTTATTAAAAAACA | 5336 |
| rs77239147 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899338 | TATATACGTATATAT[A/G]TATATACATGTACTA | 5336 |
| rs77319035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801459 | ATTTTCCATGTTGAT[A/G]TAGCTTTATTTTAAC | 5336 |
| rs77348883 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921043 | CTTTATAGCTTCTTC[C/G]TGTGTCTACTCATGG | 5336 |
| rs77353266 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900499 | GTGGGGGTTGTGCCC[A/C]CCGAGCAGCGCCCGG | 5336 |
| rs77365262 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954836 | TATACACCCAAAGGA[A/G]TATAAATCATTCTGA | 5336 |
| rs77369818 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854202 | GAGAAACAGGGTGAG[C/T]GGAAACCCCAAACTC | 5336 |
| rs77396456 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876545 | CTTGTCCAGCTGGTA[A/G]CTTCTCCTGGGGCCC | 5336 |
| rs77400508 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802595 | GTTTTGAGACTGAGT[G/T]GAGTTTCACTCTTGT | 5336 |
| rs77428584 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828685 | CAAGTTATAAAAGTC[A/G]TCTGAGACTCAGTTT | 5336 |
| rs77437293 | snp | C/T | 0.166832 | 0.235761 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786520 | GTCGAGTCATCTTTC[C/T]TCTTAAGGGCGAATT | 5336 |
| rs77463676 | snp | A/G | 0.46875 | 0.121031 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865986 | CACTGGGGCACCAGC[A/G]TGAGAGGACGCTGGC | 5336 |
| rs77467590 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942980 | GGACTTGGGCAGCGA[C/G]AGAAGGTACATAGAG | 5336 |
| rs77483597 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795313 | GCCTCAGGGTGGCCT[C/G]TCTGTAGAGGTGATG | 5336 |
| rs77510974 | snp | A/C | 0.476052 | 0.106772 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778071 | AAAAAAAACCAAAAA[A/C]ACACACACACAAAAA | 5336 |
| rs77512205 | snp | C/T | 0.226779 | 0.248919 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954123 | AACCTCCTGGGCTCA[C/T]GTGATCTTACCCTCT | 5336 |
| rs77545575 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840592 | TCTCATAAAGAGTGT[A/G]CAACCTGGGTCCCTC | 5336 |
| rs77562987 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835316 | TAATAATGAAGATGG[C/T]CGGGTGTGGTGGCTC | 5336 |
| rs77577233 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857998 | ACCACTCCCTCCATT[C/T]TTAGCTGATTCCATT | 5336 |
| rs77626614 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836439 | CCTTCCCTTGGTAGT[A/G]GTTAAGAGTGCAAGC | 5336 |
| rs77638496 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833374 | ACTGTGGCTCCGGTC[A/G]GTACACGGGTCCTGA | 5336 |
| rs77642696 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805617 | TCTGAACAGATGCCT[C/T]ACACCCCCTTCCCCC | 5336 |
| rs77687047 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827127 | TAAGACTCAGGGGAT[A/G]CCCCTCAACGGGATG | 5336 |
| rs77689689 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887696 | TAAGCACACACACAT[C/T]TGGTCGCATATTTGC | 5336 |
| rs77698337 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922730 | TGGGTGGGAGGAGAA[C/G]GAAGCTGCTCATTTA | 5336 |
| rs77709522 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819011 | CCTTCTAGGCCCACC[A/G]TGAGGCAGGTGTAAC | 5336 |
| rs77719976 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821596 | CCTACTTGTTGCCTT[G/T]TGTGCTGCTCTGAGC | 5336 |
| rs77745153 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871776 | TGAAAGGGAAAACAT[A/C/T]GGGGCCTGAGAATAT | 5336 |
| rs77745440 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954879 | tagaactagaaatac[A/C]atttgacccagcaaa | 5336 |
| rs77805205 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837959 | ATTTAGTTATGTACA[A/G]TTTGGTCACATGCAT | 5336 |
| rs77805777 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933473 | AAATCCTTCTAGTTA[A/G]TGGGTTTCCAGAGCC | 5336 |
| rs77837128 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932406 | TGCCACCCTGTCTTC[A/G]ATGATGGAGTAAGGG | 5336 |
| rs77859761 | snp | C/T | 0.093417 | 0.194889 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959610 | AGTTACTCCTCCAAC[C/T]GGGAGCTGCTATTTT | 5336 |
| rs77861546 | snp | C/G | 0.20111 | 0.245173 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794173 | GCTAGGAAAAGACCA[C/G]AAACACAGCCTGGAA | 5336 |
| rs77911016 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781424 | TTCTGTTTTTTTTTC[C/T]TTTTTTGTATTTCTA | 5336 |
| rs77956945 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815464 | GCTGAGAGACCACCC[A/C]CTAGAGGCTTCCTCA | 5336 |
| rs77962701 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827204 | GGTTTTTTTTTTTTT[G/T]GGGACAGGGTCTCAC | 5336 |
| rs77978782 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815272 | GCTCTCCCTGGTGGG[C/T]CCAGGCTAGAGCATG | 5336 |
| rs78015619 | snp | A/T | 0.00716266 | 0.059414 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960947 | TTTCTCACCTTACAA[A/T]AGAAAATATGGCTGT | 5336 |
| rs78025342 | snp | A/C | 0.0402882 | 0.136092 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959682 | GGCAGATGTTCAAAG[A/C]AACTTTCAAGAAAGG | 5336 |
| rs78064438 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820421 | ACATGGAATGAAACA[C/G]TAGACTGTGTTTTGC | 5336 |
| rs78074872 | snp | C/G | 0.126909 | 0.217598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944495 | GAGACAAGGTCTTCC[C/G]TCTGTCACTGAGGCT | 5336 |
| rs78083744 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812461 | tgagcttttttccta[C/T]gtttcttggctgcat | 5336 |
| rs78129236 | snp | G/T | 0.0729998 | 0.176553 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909587 | ACACCTGAATAACTT[G/T]TAAATTTTTTGTAGA | 5336 |
| rs78136311 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902348 | CAGGAACTGATTTCT[C/G]ACGGTTCTGGAGGCT | 5336 |
| rs78152797 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944770 | CATGAGCCACCGTAC[C/T]TGGCCAACTATGTCA | 5336 |
| rs78159944 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870328 | CTGAGGGTTTGAAAG[A/G]GTCAAGGAAATTGCC | 5336 |
| rs78177318 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868312 | TTCCCACTTCCCCTC[C/T]CTGGCCCTTAGTGAC | 5336 |
| rs78187745 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834638 | TCAGAGCTGGGGCTC[A/C]TTGAGGGATGTTCCT | 5336 |
| rs78192875 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815140 | ATTTAGGCTTAAAAT[A/G]AAGCACCTGTGATAT | 5336 |
| rs78262883 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841806 | TTCCCCCAGCTGCCA[G/T]GTCAGACGCTGCTAC | 5336 |
| rs78287508 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925518 | TGAATTGGTAGCATC[A/G]GTCCTCACTCTGCTT | 5336 |
| rs78300827 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807686 | ATTAGTCTGTTCTCA[C/T]GGCTATAAAGAGCTA | 5336 |
| rs78315151 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862970 | ATCTTCCCTTCCCCA[C/T]CCTGACCAATCACCT | 5336 |
| rs78354261 | snp | G/T | 0.113567 | 0.210272 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874760 | TAACCACCTGCCTAC[G/T]TTCCACCTCTCGAGC | 5336 |
| rs78369473 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848092 | CAAGACTTACTCTAA[C/T]GTTCCAGTAATCAGT | 5336 |
| rs78432615 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913557 | AGTCTCTAGCCAGAG[G/T]CCTGGGGGCCAAATC | 5336 |
| rs78439640 | snp | A/G | 0.0295035 | 0.117819 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960020 | CTCTCTCCAGCTGCT[A/G]CTGTGTAAAATCCAT | 5336 |
| rs78454823 | snp | A/G | 0.0579041 | 0.160767 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802404 | GGCGTGAGCCACCGC[A/G]CCCGGCCTCAGGTGG | 5336 |
| rs78463230 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831240 | TAGAATGTAATTCTT[C/T]GAGGCCAGGAATTTG | 5336 |
| rs78477851 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844719 | TAAAAAAAGAGTTAA[A/T]AAGTTATAGTAGACA | 5336 |
| rs78499251 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819025 | CATGAGGCAGGTGTA[A/G]CTCCTTCAATTTGCA | 5336 |
| rs78505092 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871167 | TTCATATGCCTTCCT[G/T]GTGGAAATGCGAATG | 5336 |
| rs78518082 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877924 | TCATCACATGGACCC[C/G]TTTTCTCTGTGTGCT | 5336 |
| rs78520081 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817447 | TTGTTGCGCACGCTG[C/G]AGTGCATCGTCTTGA | 5336 |
| rs78539888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870440 | ACAAATATGTCTGAA[A/G]TTGGAAGTCCAAAGA | 5336 |
| rs78547923 | snp | C/G | 0.249886 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792404 | CAGAATTGCTTGAAT[C/G]TGCAAGGCGGAGGCT | 5336 |
| rs78579348 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852344 | GGGTCATTCCCTGGC[C/G]CCTGCTGTCGCCTTC | 5336 |
| rs78596582 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778601 | GGACATCAATTGTCT[-/G]GGGGTTCTTTGCTCC | 5336 |
| rs78610796 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787626 | GCATGTATAGTGTGG[G/T]GGTTTTAGTATATTT | 5336 |
| rs78620323 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781767 | TTGTGGGATTTTTGG[A/G]TGAAATCCTGTACTG | 5336 |
| rs78628719 | snp | A/G | 0.084364 | 0.187256 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959667 | AACATTCCTCTTAGT[A/G]GCAGATGTTCAAAGC | 5336 |
| rs78639753 | snp | A/C | 0.040671 | 0.13668 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829624 | ACTTTAACAGTTTCT[A/C]CTCGTATGTTCTCCT | 5336 |
| rs78649754 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789954 | ATCTCCGTGGAGCCT[A/G]TATTGCTTTATTAGG | 5336 |
| rs78653935 | snp | C/T | 0.102014 | 0.201495 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878718 | CCCGTGGTCTTTATC[C/T]TGTCCACTCAGCAGC | 5336 |
| rs78659947 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806879 | CCAAGCAGGGTGATG[A/G]GGGCAGAGTTATGGG | 5336 |
| rs78690039 | snp | A/C | 0.0422178 | 0.139109 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940657 | CCAAGCTGGGTCATA[A/C]GACCAGCTCTTAAGA | 5336 |
| rs78716929 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871054 | TTTTAGTCAAGGAAA[C/T]ATAAATGAGAATGAT | 5336 |
| rs78717038 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954503 | ACATGCATTCCCCAT[C/T]CGCCAACTAGCCATG | 5336 |
| rs78720750 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891339 | AAAACGTGGGTAACT[A/G]AGGTCTGGAGACCGC | 5336 |
| rs78744279 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793556 | TTTTCACTTTTGCTT[A/G]GGCATATCTTCTCTG | 5336 |
| rs78744373 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781880 | TCCCCCCCCCCCCCC[C/G]CCCGCCCCCGAGACG | 5336 |
| rs78761750 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896847 | CCATTTAACAGATGA[A/G]TAAATTGAGACAAGG | 5336 |
| rs78762417 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909341 | TGTGAGGAAGGCTCT[A/G]ATGCCCTGACGTGGG | 5336 |
| rs78779783 | snp | A/T | 0.188 | 0.24219 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788699 | ATGTATCCTATCATG[A/T]GTGTGATCAAACTGC | 5336 |
| rs78786964 | snp | A/C/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933338 | AGAAGGCCCCATCCC[A/C/G]CTCTTGGGAAACCAG | 5336 |
| rs78791105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899807 | GGCTGTGAGCCCAGT[A/G]TCAGTCAATAATATA | 5336 |
| rs78798891 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873015 | CATTTCCTATCTGCC[C/T]AGATTTGGGGAAAAC | 5336 |
| rs78827236 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918844 | GGAGGCTCTTCTGTT[A/T]TGGATTTTTTCTGCT | 5336 |
| rs78835630 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928145 | TCTTAAAAGCCAGGT[C/G]ATAGAGCATGGGTGT | 5336 |
| rs78842618 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856780 | AAAAGGAGACTTGGC[A/G]GGTGTGGTTAAATTG | 5336 |
| rs78861486 | snp | A/G | 0.385168 | 0.210309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857031 | GATCTCATGCAACCA[A/G]TCTATTTTAGACTTC | 5336 |
| rs78891211 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909644 | CTGGTTTTGAACTCA[C/G]CTCAAGCAATCCTCT | 5336 |
| rs78907058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957490 | TTTAAGGAGTACTTA[C/T]TGTGTTTCCAAGAAT | 5336 |
| rs78921819 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945919 | TTTAATTTCTTCTGA[A/G]TGAATCATTTTTATT | 5336 |
| rs78951794 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879269 | TCAGCAGCAGGCTGA[C/G]TTGGTGACCTAAGCA | 5336 |
| rs78959456 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865966 | CTTTCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs79013350 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846274 | GAGGACCTACTTTTC[C/T]GGTGTGATTCATGCT | 5336 |
| rs79030206 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851052 | CTCAGTGGGGTGTGA[C/T]GGGGGATGAGTCCTT | 5336 |
| rs79056726 | snp | A/C | 0.129664 | 0.219133 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849449 | AAGGACAGATGCTCA[A/C]CATAGGCCAGTTCAA | 5336 |
| rs79066731 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892138 | CAGCATGTGCCAAGG[C/G]CCTGGGGCAGGAACA | 5336 |
| rs79071379 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786474 | TGTGCCCTGTCTGAC[A/G]GCATCAGGGATCGTC | 5336 |
| rs79074012 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782847 | GCACCTTACACCCAC[A/C]CTGCAGCATCAGAGG | 5336 |
| rs79075508 | snp | C/T | 0.19646 | 0.2442 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799225 | AAAACAACCCCTTAG[C/T]CCCCGCCACCCCCCT | 5336 |
| rs79078538 | in-del | -/C/CC/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781389 | TCCAGGAGGCCCCCC[-/C/CC/G]ACATTGATGAGCAGT | 5336 |
| rs79080750 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954821 | ATATAAATCATTCTG[A/C]TATAAAGACACATGC | 5336 |
| rs79087303 | snp | A/G | 0.253264 | 0.249979 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811367 | GGGATGGTTTTGCAC[A/G]TCGGGGTTCAGGACT | 5336 |
| rs79105869 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798898 | TTTCACCGGCCAGGT[A/G]TCTCTCTCCCCAGCA | 5336 |
| rs79107663 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929799 | TGGGAAAATCAAGGT[C/G]CTAAGTGACCGACCA | 5336 |
| rs79108496 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859539 | AGTAAACCAGGTGGT[C/T]CTTTTTTTTTTTTGA | 5336 |
| rs79117687 | snp | C/T | 0.0194272 | 0.0966238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873991 | CAAAATGTCAGAACC[C/T]TCTGGGGTGCCCTAG | 5336 |
| rs79124095 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868884 | GTAGGTGCCTCCTCA[C/T]TGGGGCATCACTGTA | 5336 |
| rs79130147 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855226 | GAAGAAAAAGAAAAA[C/T]GTAACCTGTTTTCTT | 5336 |
| rs79148604 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817773 | GTTACAGGCATAAGC[A/C/G]CCTGCACTCGGTTGT | 5336 |
| rs79159225 | snp | C/G | 0.089084 | 0.191327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818484 | GCTGTCTGCATGGGT[C/G]AATGCCATTCTTCCT | 5336 |
| rs79161751 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890392 | TTAAGGGCAGTTTGG[A/G]GGTTAAAGGCAAGAT | 5336 |
| rs79169767 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898659 | GCCATGCACAAGCCT[C/T]AGATGGATTCTTGGT | 5336 |
| rs79179080 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956503 | ACTTTTTAAACTGCT[A/T]GCTTCCCACACAATA | 5336 |
| rs79198598 | in-del | -/TG | 0.489434 | 0.0719116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782244 | TGAGATACAAGAAAA[-/TG]ACCTTTAGAAGGACA | 5336 |
| rs79234931 | snp | C/T | 0.0189856 | 0.0955633 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959296 | CTGACCCTCCTCTTG[C/T]TACCCGAAATGCTGG | 5336 |
| rs79254873 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929676 | GCTGGGATGACAGGC[A/G]TGTGCCACCATGCCC | 5336 |
| rs79255258 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821730 | CAGAGCCCCAAAATA[C/G]ATCTTTCTCCGCTAA | 5336 |
| rs79256102 | snp | A/C | 0.172028 | 0.23753 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807332 | GTGTGCATCTCTGCG[A/C]GGAGGGCACTGAGGA | 5336 |
| rs79281920 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859604 | CAGTGGCATGATCTC[A/G]GCTCACTGCGAGCTC | 5336 |
| rs79283826 | snp | C/T | 0.267874 | 0.24936 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900111 | ATGTATGCATGCACA[C/T]ATGCAAATTACATAT | 5336 |
| rs79341966 | snp | C/G | 0.159292 | 0.232964 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779901 | GGCGCAGTCCTTCCC[C/G]GAGACTTTTGGAGAG | 5336 |
| rs79351249 | snp | A/G | 0.182614 | 0.240747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859596 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 5336 |
| rs79369548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796731 | GGCCATGTGAAGACA[A/G]ATACAGAAATCTGAG | 5336 |
| rs79390187 | snp | A/C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824346 | ACCACGTTGGCCAGG[A/C/T]TGGTCTTGAACTCCT | 5336 |
| rs79391759 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824732 | TTTTTGTCCTTCCCC[A/C]TGATGTCACCTTTCA | 5336 |
| rs79412961 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824748 | TGATGTCACCTTTCA[C/T]TGGATGGTGACTCCC | 5336 |
| rs79422978 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812294 | gacctcgtgatccac[A/C]cgcctcagcctccca | 5336 |
| rs79434273 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829477 | CCCTCCTTGGCCTCC[C/T]GAAGTGTTGGGATTA | 5336 |
| rs79444755 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856077 | TCTTGGTCCCTCTTC[C/T]GGAACCCTAAATTCA | 5336 |
| rs79446864 | snp | C/G | 0.198944 | 0.244731 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846708 | AGTTCTTCCTGGCTT[C/G]ATCTATAGATTCAAC | 5336 |
| rs79451837 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812068 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 5336 |
| rs79465773 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839989 | TTGAGCCTACGAGTT[C/T]AAGGATGCAGTGAGC | 5336 |
| rs79479456 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815756 | GTAGGTCTTAAGTGC[A/G]CTATAATTGAGCAGT | 5336 |
| rs79481043 | snp | C/G/T | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800984 | AAGGAATGCAGGTGG[C/G/T]TTGTGCAAGCTGGAA | 5336 |
| rs79504588 | snp | C/T | 0.185788 | 0.241613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791485 | CATTTGGTGTCACCT[C/T]GCCTGGAAGGTTCCA | 5336 |
| rs79575976 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954854 | AGCAATCCCATTACT[A/G]GGTATATACCCAAAG | 5336 |
| rs79651141 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862072 | GAGGGAGCTTTGCAA[A/G]AGAAACTTTGACCAA | 5336 |
| rs79667821 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835255 | AGGTGAAGCAGTTAA[C/T]ATACTACCTTACGTA | 5336 |
| rs79668374 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898741 | AGTATGTCTAATGAT[C/T]AGTATGTCTAATGAT | 5336 |
| rs79668956 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881093 | CTGCTGGGGAATTGG[C/T]CATCCCATGCCTGTG | 5336 |
| rs79726200 | snp | A/C | 0.221439 | 0.248363 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778073 | AAAAAACCAAAAACA[A/C]ACACACACAAAAAAA | 5336 |
| rs79732035 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907502 | AAGCTCAAAATGCAT[C/T]GATATTTTAAAAAAG | 5336 |
| rs79737853 | snp | C/T | 0.109461 | 0.206758 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857029 | GAGATCTCATGCAAC[C/T]AGTCTATTTTAGACT | 5336 |
| rs79750033 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792710 | GCCTCTTGTAAAACT[A/G]TCAGCCCTCATGAGA | 5336 |
| rs79766885 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798788 | AGGAAGAGGAGACCC[C/T]GCAGAGCTCAGAAGA | 5336 |
| rs79773175 | snp | A/G | 0.177824 | 0.239355 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813699 | TACCTGAATATATTC[A/G]TTGGATGGCCAGGCT | 5336 |
| rs79773699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810609 | AGGTGTCCTTTCTGC[C/T]GTCCACTTAGTGCCT | 5336 |
| rs79776741 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824519 | AGCTTTTGTGGAGCC[A/T]GGTGTGGCTGGCACT | 5336 |
| rs79783478 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947349 | TAGTTCAGCTGCTAG[A/G]TCTTGAGATTTCATT | 5336 |
| rs79800996 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934657 | TCCCAGTAGATGGCC[C/T]CACCTTGGGTTTGTC | 5336 |
| rs79811595 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916655 | GACATATTTTTTTTT[G/T]GAAATGGAGTCTTGC | 5336 |
| rs79818114 | snp | A/G | 0.039522 | 0.134904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906721 | GGGCCACTGTACCCA[A/G]CCAAAAATGGCAATA | 5336 |
| rs79821482 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954801 | AAGACACATGCACAC[A/G]TAAGTTTACTGCAGC | 5336 |
| rs79821524 | snp | A/C | 0.115438 | 0.210697 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811216 | TCCCTCCTTGGGTCT[A/C]AGTGTCTGCATCTGT | 5336 |
| rs79851943 | snp | A/T | 0.129664 | 0.219133 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849233 | GGATAACGTACTGCT[A/T]TAAGGAGACAAGTCA | 5336 |
| rs79885646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911376 | GATTTTCTGAGACAC[A/G]TGGCAATAACTGTGC | 5336 |
| rs79901660 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865440 | GCTAGGAGCCCAAAG[A/G]AGCTCTCAGCCTCCA | 5336 |
| rs79911174 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895596 | AAAAGCAGCATTGAA[A/G]CTAGCTTGTCTTGGA | 5336 |
| rs79914340 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918908 | TGTTTCTTTTTTTTT[A/T]TAAAAAAAGTCACTG | 5336 |
| rs79951189 | in-del | -/C | 0.43088 | 0.172575 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852486 | AAGGGACTGGTTGAG[-/C]TTGTTGAGCTTGTGT | 5336 |
| rs79954624 | snp | C/T | 0.130008 | 0.219321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847970 | AATATTACAGAATCC[C/T]AGCAAGTTATTCTGT | 5336 |
| rs79955584 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807504 | CATCACTGTCACTAA[C/T]GCCACCATAAGAGCT | 5336 |
| rs80018030 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916826 | TATTTTTGGTAAAGG[C/T]GGGGTTTCACCATGT | 5336 |
| rs80047454 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849849 | AAGAGAATTGTTAGA[C/G]TAGACAGAAAGAGAA | 5336 |
| rs80049313 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821981 | AAATTCCTTAACTTC[A/G]CTGAGCCTTCTCTTT | 5336 |
| rs80062355 | snp | A/G | 0.078151 | 0.181571 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957561 | ACAGGGATGCTTGTG[A/G]TTGTGCTACAGGCAT | 5336 |
| rs80070108 | snp | A/G | 0.00659791 | 0.0570563 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921345 | TCTTGTTCCCATGGC[A/G]GTTATAACAGGGCAA | 5336 |
| rs80070900 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951830 | AGATGCCATAAATGT[A/C]AACAGCCAAATGAAA | 5336 |
| rs80079672 | in-del | -/GTTTT | 0.291493 | 0.246533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951490 | TGGTTTTATAGCTTA[-/GTTTT]GTCTTCATTTAAATA | 5336 |
| rs80080055 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794126 | AAGGAGACTCAGTGC[G/T]CATCCTAGAGGCGCC | 5336 |
| rs80084509 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799208 | CCTACTTCTGGGTGA[A/G]AAAAACAACCCCTTA | 5336 |
| rs80095587 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907373 | AGACAAACTGGCTGG[G/T]AAATCCTGAAAGTTT | 5336 |
| rs80107436 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922539 | CAACCCTGTGAAATA[C/T]ATAAAAATTTAATTC | 5336 |
| rs80118901 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859540 | GTAAACCAGGTGGTT[C/G]TTTTTTTTTTTTGAG | 5336 |
| rs80134881 | snp | C/T | 0.0387552 | 0.1337 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958183 | CCTATTATTTTCATC[C/T]TGGACAACTTTCTTA | 5336 |
| rs80159077 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901726 | TCCCGTTTACAGTTA[C/T]TGCAAATATTTCAAA | 5336 |
| rs80162145 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916304 | TAAAAAAAGAAAAAA[-/AA]CAACGTTTTTTAAAA | 5336 |
| rs80179667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861561 | ATGCCCTGCCTGCTC[C/T]GCCACGCTGGGCCAC | 5336 |
| rs80194345 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841016 | TAGTTCTGCATGAAT[A/G]TGAAGCATTAGAATC | 5336 |
| rs80195425 | snp | G/T | 0.225005 | 0.248747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916589 | TTAACCATTTTTTTT[G/T]TGTGTGTGGTGAGAC | 5336 |
| rs80201510 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945068 | AATGACAATACACCT[G/T]AGGGGTGTAAAAGGA | 5336 |
| rs80212463 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854316 | CTGAGTCCAGACGCA[C/G]AGATAGCTTTGCGGG | 5336 |
| rs80222169 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818808 | GTGGAGGGCAGCCTC[A/G]TGAGAACTGGTATTT | 5336 |
| rs80268988 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929269 | CTCTGTAGCGGGCCT[C/G]CTTGTTCTGGGCAGC | 5336 |
| rs80270711 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915670 | ACGATGATCCTAATG[C/T]TCCCCATGCGACGGG | 5336 |
| rs80275783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795729 | CCCAAGAGATGGGGT[A/C]TTGCTTATTGCCCAG | 5336 |
| rs80278285 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870602 | AGGGGGATTAGGGAA[C/T]GTGTGGAGGGTTTTG | 5336 |
| rs80292842 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818648 | CCAACTAGCCGGGCA[C/T]ACCTTTTCTCTGCAG | 5336 |
| rs80297959 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841346 | GGCTCAAGCCGTTCT[C/T]CTCAGCCTCCTGAGT | 5336 |
| rs80314689 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837070 | GAATTTATTCCAGGC[C/T]ATCCAAGTTAAGGTA | 5336 |
| rs80327777 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806027 | AAATTTTATTTAACT[C/T]AGTATATCCAAAGCA | 5336 |
| rs80332679 | snp | C/T | 0.209693 | 0.246729 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830679 | GTGTATATATATATA[C/T]ACACACATATATTTT | 5336 |
| rs80343087 | snp | G/T | 0.188316 | 0.242271 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790449 | TCACACCTTGAGAGA[G/T]CAGGCCTTCAGGCCC | 5336 |
| rs80346932 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853591 | CACCGTAGGGTTTGC[A/C/G]CCCCTATGAGAATCT | 5336 |
| rs111236624 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912114 | ATTTTTGTATTTTTA[A/G]TAGAGACAGAGTTTC | 5336 |
| rs111241223 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875521 | TAGAAGTAGAGAGAA[C/T]AGCGTAACAGACCCC | 5336 |
| rs111247260 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909584 | ACGACACCTGAATAA[-/C]TTTTAAATTTTTTGT | 5336 |
| rs111288642 | snp | A/C | 0 | 0 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778021 | GACTTTGTCTCAAAA[A/C]AAAAAAAAAACAAAA | 5336 |
| rs111324427 | snp | A/G | 0.135825 | 0.222405 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911867 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTT | 5336 |
| rs111327850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829296 | GTATTTTTAGTAGAG[A/G]TGGGATTTCACCCTG | 5336 |
| rs111330124 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866654 | TCCCAGGATGAGCTC[C/T]ACTGGGGCACCAGCG | 5336 |
| rs111332042 | in-del | -/C | 0.461923 | 0.132621 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781383 | TATTTATCCAGGAGG[-/C]CCCCCCACATTGATG | 5336 |
| rs111338797 | in-del | -/CA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899303 | ATACACACACACACA[-/CA]TAAATATATATGTGT | 5336 |
| rs111362226 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827790 | TGAAATCTCCTCATT[A/T]AAAAAAAAGCGTTGA | 5336 |
| rs111362391 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846194 | CTAGGAGGTTGTAGT[A/G]GCTGTAAGCCAAGCC | 5336 |
| rs111364529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857133 | CAGCAGAGGAGACTG[A/C]TGACTGAACCTTTGA | 5336 |
| rs111375906 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824187 | CACCCAGGCTGGAGT[A/G]CAATGGCGTGATCTC | 5336 |
| rs111388585 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840482 | ACAACTCACCGTAAT[A/G]TAGAATCAGTGGGAG | 5336 |
| rs111407264 | snp | C/G | 0.154993 | 0.231244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811102 | ACCCTGAGGTGTTCA[C/G]TGTGCTGGGGAAGGT | 5336 |
| rs111415571 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924691 | AGAACCTCATTGCAA[A/T]CCAATTCATACCTAG | 5336 |
| rs111416494 | in-del | -/TG | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884601 | TCAATTGTATGGATC[-/TG]TGTGTGTGTGTGTGT | 5336 |
| rs111438649 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830668 | TGTGTGTGTGTGTGT[A/G]TATATATATATACAC | 5336 |
| rs111441423 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814587 | GTAATCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 5336 |
| rs111456261 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910176 | GCTCACTGCAACCTT[C/T]GTCTCCCAGGTACAA | 5336 |
| rs111456474 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866400 | ATGAGAGGATGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs111459311 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945678 | TTGTAAAGAGGGAAT[A/G]GCTTTAGGAGGAGGA | 5336 |
| rs111464711 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866649 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs111465927 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882403 | CCTGGAGTCTGGTGG[A/G]GCCTCATGTGGCTCC | 5336 |
| rs111469764 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902090 | GGCAAATGGTTTCTG[A/G]TAAGCAAGTCAGCTG | 5336 |
| rs111487552 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904172 | TATCATGCTGCCATT[A/C]ACAAGGGACACTGAG | 5336 |
| rs111491648 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780612 | GATGCAGCTGCCTTC[C/T]CCCACCAGCGACTGG | 5336 |
| rs111504749 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777664 | TTGTGAAGTCACAAA[C/T]GAGTCCTATGGCTTG | 5336 |
| rs111511893 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896536 | TGAGGTCACATTGCG[C/G]CACTGCACTGCAGCC | 5336 |
| rs111518977 | in-del | -/GTGGAGGTACCCAAAGAGGAGGAA | 0.0437281 | 0.141251 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835045 | TCTCAGTGGGAGGAG[-/GTGGAGGTACCCAAAGAGGAGGAA]GTGGCCTTCCAGGTG | 5336 |
| rs111533716 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893260 | GATATGGCTCCTAGC[A/G]TAGCCGATTGCACCA | 5336 |
| rs111542751 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846287 | TCCGGTGTGATTCAT[G/T]CTCCAGACATCCCCC | 5336 |
| rs111553163 | snp | C/T | 0.000413931 | 0.0143803 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81880939 | CAAAAAGGATTCGTC[C/T]GTGTTCATCCTGGGG | 5336 |
| rs111563675 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866451 | ACCAGCATGAGAGGA[C/T]GCTAGCCTCTCCCTT | 5336 |
| rs111580740 | snp | C/T | 0.141596 | 0.225274 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827919 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 5336 |
| rs111602780 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824190 | CCAGGCTGGAGTGCA[A/C/G]TGGCGTGATCTCAGC | 5336 |
| rs111609476 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866514 | ATGAGAGGACGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs111611330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944023 | CCAATGAAGGCATCC[A/G]CGGAATTCAGTAAGA | 5336 |
| rs111611909 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838165 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 5336 |
| rs111617380 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933559 | AGGCCTGGAGAGTAA[C/T]TGTCATGCTGTTTTT | 5336 |
| rs111619838 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960400 | GCAGCACTGATAGAT[A/C]AAAACCACCACTGCA | 5336 |
| rs111622557 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802113 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 5336 |
| rs111628568 | in-del | -/CTT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837706 | TTTTTTTTTTTTCTC[-/CTT]GATGCTGTGCATTTT | 5336 |
| rs111634911 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833405 | GCCAGTATTCTGGCC[C/T]GGGGTGGCCGTTCCC | 5336 |
| rs111637055 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957589 | CATGTAATGGGGTGC[A/G]GGGCGGCCGGGGTTG | 5336 |
| rs111638889 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804128 | TAAGGAATTGCCAAG[A/T]CTGTTTGCCAAAGCA | 5336 |
| rs111639914 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925659 | TTGGGAGGCCGAGGC[A/G]GGTGGCTCACTTGAG | 5336 |
| rs111663298 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910466 | CTGAGGCCCTGGCTG[C/T]CGCAATGGCCTGGCC | 5336 |
| rs111670531 | snp | C/G | 0.310386 | 0.242597 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888432 | GGGTTTCACCATGTT[C/G]GCCAGGCTGGTCTCA | 5336 |
| rs111672433 | in-del | -/AAG | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925892 | TCTGTCTCAAAAAAA[-/AAG]AAAAAAAAAAAATCC | 5336 |
| rs111678972 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894284 | AAGTAAAAAAATTAG[-/C]CTGTGTGTAGTGGCA | 5336 |
| rs111697677 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890452 | TGTCATAATTTTCTT[G/T]TTGTTCTGATTTTGG | 5336 |
| rs111698525 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778376 | CCCTGCCTCTTAGAA[A/T]ACAGAAGCTATAACT | 5336 |
| rs111703614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781108 | AGAGAAAAATTTGCC[C/T]GTTACATCATCAGTT | 5336 |
| rs111706353 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866353 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGTTGAGCT | 5336 |
| rs111723349 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866682 | GCGTGAGAGGACGCT[A/G]GCCTCTCCCTTGCTC | 5336 |
| rs111732831 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830693 | ATACACACATATATT[A/T]TATATATGTATATAT | 5336 |
| rs111750011 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851489 | CGTGCTGTTTTTTTA[C/G]TCTTTTCACATGGCC | 5336 |
| rs111800643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851716 | TGGGGTTTCACCTTG[C/T]TGGCCAGGCTGGTCT | 5336 |
| rs111841794 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798094 | CATTGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 5336 |
| rs111849947 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81779570 | GCACCCTCGGGGACC[C/T]CGGCCCGCCGTGCCC | 5336 |
| rs111856762 | snp | A/G | 0.100231 | 0.200173 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929430 | CGATAGAGTCTCGCT[A/G]TGTCACCCAGGCTGG | 5336 |
| rs111861589 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955668 | TTGACTCAATAGCAA[C/T]GTGGCCATGACAGGA | 5336 |
| rs111863188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826776 | GTAGCAAGAACCTTC[C/T]CAAAGCCACTTAGCT | 5336 |
| rs111868520 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845756 | TGCCCCTGCCTGATG[A/T]AAGATCAAGGGGTGG | 5336 |
| rs111894845 | snp | C/T | 3.3423e-05 | 0.00408783 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883367 | AAGGTGTGTGGGTGC[C/T]TGAGGGAGCTGGCGG | 5336 |
| rs111918467 | snp | C/G | 0.250168 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792389 | TGGGAGGCTGAGGCA[C/G]AGAATTGCTTGAATG | 5336 |
| rs111922848 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807048 | GGCTTTCTCCTGAGT[C/T]GTCCATTCTACCTTC | 5336 |
| rs111929204 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810152 | ACTCACCACCACGCC[C/T]AGCTAATTTTGTATT | 5336 |
| rs111931465 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827085 | TGTGGCCTAGGGCTG[C/T]ATGTCCTTGTTGACC | 5336 |
| rs111946415 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929557 | TGGGCCACCGTGCCT[A/G]GCTAATTTTTGTATT | 5336 |
| rs111947694 | in-del | -/CTTCTTTTT | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823981 | TCCTTCCTTCTTTTC[-/CTTCTTTTT]CTGTTTCTTTTTCTT | 5336 |
| rs111962646 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878088 | CCGGGTTCACGCCAT[C/T]CTTCTGCCTCAGCCT | 5336 |
| rs111969284 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901185 | GCTGGAGGTGTCCAG[C/T]GACCTGGGTGCTGTT | 5336 |
| rs111998378 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912921 | CGTTCTCCAGGGCAG[G/T]ATGTTCTGTAGTAAC | 5336 |
| rs112004836 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839386 | ATATAGTCTTTGTAT[A/G]ATGAGAGTTTTCTGT | 5336 |
| rs112007343 | in-del | -/ACAA/ACAAAC/ACAAACAA/ACAAACAAAC | 0.506537 | 0.137117 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781028 | AGACTCCATCTCAAG[lengthTooLong]ACAAACAAACAAACA | 5336 |
| rs112011952 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862612 | TGGTGGCTGACACCT[A/G]TAATCCTAACAGTTT | 5336 |
| rs112021989 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826320 | AGAGATGGGGGAACC[G/T]AGAAAAGCATCAAGT | 5336 |
| rs112025109 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866170 | GCATGAGAGGACGCT[A/G]GCCTCTCCCTTGCTC | 5336 |
| rs112030485 | snp | C/T | 0.234982 | 0.249549 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812338 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCTGTTG | 5336 |
| rs112036633 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954218 | TATAGTAACAGGGTC[C/G]CGCTATGTTGCCCAG | 5336 |
| rs112041150 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780925 | CCAGCTACCCAGGAG[A/G]CTGAGGCAGGAGAAT | 5336 |
| rs112091089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883538 | CTGTCTGATGCCACT[A/G]AAACTCTGGATGAGA | 5336 |
| rs112101745 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838180 | GCCTCCTGGGTTCAA[C/G]TGATTCTCTTGCCTC | 5336 |
| rs112103926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874660 | TGGTGACTTATAATC[A/C]CCAGAACTAAATCCA | 5336 |
| rs112113196 | snp | A/G | 0.00329471 | 0.0404537 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908640 | TTCTCCATGCCAACC[A/G]ATGAGGCAGGGTGGC | 5336 |
| rs112113666 | in-del | -/GCTGCT/GCTGCTGCT/GCTGCTGCTGCTGCT/GCTGCTGCTGCTGCTGCT | 0.57878 | 0.166018 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834591 | CCCTGGATCTGCAGA[lengthTooLong]GCTGCTGCTGCTGCT | 5336 |
| rs112115039 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905084 | TAGATACAGGGTTTT[C/G]CCATGTTGGCCAGGC | 5336 |
| rs112127659 | snp | C/T | 0.131723 | 0.220251 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813371 | GTTTGTAGTTCTCTT[C/T]GAAGAGGTCCTTCAC | 5336 |
| rs112128079 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804027 | GGACATTCATGTACA[A/C]GTTTTTGTGTGAACA | 5336 |
| rs112135616 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942949 | TACAAGGAGGGCTGC[C/T]CAGTGCATAAAAATG | 5336 |
| rs112190603 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909308 | GTTTAATGTGAGTTG[A/G]GGGGATTTGTGAAAG | 5336 |
| rs112196117 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860971 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAGCAA | 5336 |
| rs112236064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954713 | CATGGTGTATATGTA[C/T]CACATTTTCTTTATC | 5336 |
| rs112247612 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877789 | GCATCGCTCCTTGGC[G/T]TGTAGATGTCATTGC | 5336 |
| rs112249898 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953418 | TTACTGTACCTTTTT[A/T]GTAAGCTTAAGCTTC | 5336 |
| rs112260550 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839778 | CATTTAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 5336 |
| rs112265830 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846838 | AAGGTGTGTTTTTTT[G/T]CTCTTTCTCTTTCCT | 5336 |
| rs112272072 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845157 | GTTGCCCAGGTTGGT[A/C]TTGAACTCTCTGGTT | 5336 |
| rs112280570 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902883 | GGCAAGAGAGCTTGT[C/T]CAGGGAAACTCCCAT | 5336 |
| rs112287263 | snp | C/G | 0.157642 | 0.232314 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815961 | TGGCTACTCAGGAGG[C/G]TGAGGCAAGAGAATT | 5336 |
| rs112291962 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789832 | TTTCTTTCTCCTTCC[C/T]TTCCCACCTTTGCCC | 5336 |
| rs112292373 | snp | A/C/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936045 | TCATCAGAACCCCTT[A/C/G]AATGTCAAAGAGGGA | 5336 |
| rs112299980 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780094 | GGATTCCAGCAGGAC[A/G]GTGGGGCGGGGCTCT | 5336 |
| rs112311537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808536 | TCTCCCTCTGTCGCC[C/T]AGGCTGGAGTGCGGT | 5336 |
| rs112315567 | snp | A/C | 0.0487025 | 0.148254 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959969 | TACCATATCAAAGAA[A/C]CTGACATATGGCGGC | 5336 |
| rs112344221 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866508 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs112360216 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878667 | ATCTTGGCACGTCAG[A/C]CATCACCTCCATGTG | 5336 |
| rs112365458 | snp | C/G | 0.193966 | 0.243639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803796 | AAGTGATTCTCGTGC[C/G]TCAGCCTCCTGAGTG | 5336 |
| rs112374290 | snp | A/C | 0.5 | 0 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895874 | GCGGACTACCAAGAT[A/C]AAGTTTGACGACGTC | 5336 |
| rs112378666 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779967 | TCTGCGTAATTATGC[A/G]TGTGTCTGTGCGTGT | 5336 |
| rs112408302 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876560 | ACTTCTCCTGGGGCC[C/T]GACTCAGAGATGACA | 5336 |
| rs112412945 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799732 | CGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCACC | 5336 |
| rs112423646 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812027 | TACATCCTCTCCAGC[A/G]TCTGTTGTTTCCTGA | 5336 |
| rs112424333 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784334 | GACCCTGGTAAATGC[C/T]GCAGGCTGTGCATAC | 5336 |
| rs112432467 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843740 | CAATGAAATGATCTG[C/T]TTAAAATACTAAAGA | 5336 |
| rs112440815 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783592 | TCTACATGACTTTGA[G/T]CAAGTAATGTGACCT | 5336 |
| rs112453425 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892337 | GATGGTTACTCTGAT[G/T]GCAACAGAAGGAGGA | 5336 |
| rs112457837 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946535 | GTTCCCCATAGTTTC[A/C]CTTCAGCAAGAGCCA | 5336 |
| rs112459140 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866476 | TCCCTTTCTCCCAGG[A/G]TGGTCTCCACTGGGG | 5336 |
| rs112469001 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933677 | TGTGGATTGACTTAG[G/T]TAATATCCCTCAAGT | 5336 |
| rs112481697 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849750 | CACTCCAGCCTGGGC[A/T]ACAAGAGCAAAACTC | 5336 |
| rs112485612 | snp | C/T | 0.137867 | 0.223442 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865844 | CCTCTCCCTTGCTCC[C/T]AGGGTGAGCTCCAAC | 5336 |
| rs112487444 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955432 | AGAGTAGTCAGGGAT[A/C]CTCTGAAACAGATGA | 5336 |
| rs112545988 | snp | C/G | 0.039522 | 0.134904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926886 | ATCAGCCCCCAGTAA[C/G]TCATTAGTAATTAAA | 5336 |
| rs112562122 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858526 | GTGTGGGCTCTACAG[G/T]TTTTCAAATAAGAGC | 5336 |
| rs112574023 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954373 | ACTTTATTCTGTAAA[A/G]TTTTACTTTAAGTTC | 5336 |
| rs112574887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808417 | TGTACTGGAGAGGCT[G/T]TGTGGCCCCAAGCCC | 5336 |
| rs112602737 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898171 | AACATTATCTCATTC[A/G]TGACTAGAGGAAGTT | 5336 |
| rs112608620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878817 | TATCTTGCCTCTCAC[C/T]GTTGGTTCTCTTGCA | 5336 |
| rs112609736 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860033 | TGGAGGGCAGTGGCA[C/G]AGTCATAGCTCGCTG | 5336 |
| rs112609922 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866536 | CTTGCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs112627200 | snp | A/G | 5.90092e-05 | 0.00543149 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783120 | TGGTCCCTTGTCCTG[A/G]TTTCTGTCTAATTGA | 5336 |
| rs112637460 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801576 | ATACTCCCGATTCCA[A/G]CAAACACGTCTTCGC | 5336 |
| rs112640731 | in-del | -/AC | 0.364609 | 0.222182 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880569 | TATGTAAAGCTTGAA[-/AC]ACAGCAAAAAATTGT | 5336 |
| rs112648604 | snp | A/C | 0.5 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81891484 | TAGTTCCTCACGTAC[A/C]TGTTTTCACGAGAAA | 5336 |
| rs112662663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841514 | CCAAGGTGCTGGGAT[G/T]ACAGGCATGAACCAC | 5336 |
| rs112662891 | in-del | -/A/AA | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853330 | GTGAGATTCTGTCTC[-/A/AA]AAAAAAAAAAAACAA | 5336 |
| rs112665689 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836677 | ACTCAGGAGGCTGAG[A/G]TGCAGTGAGCTGAGA | 5336 |
| rs112671601 | in-del | -/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942918 | GAAGAAAAACAATTA[-/T]TTTTTTTTTTTTTTA | 5336 |
| rs112679072 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866011 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGGGCT | 5336 |
| rs112690808 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914111 | TCAGTCCGCTGCACA[C/T]GGATTGAAAACCTGC | 5336 |
| rs112701561 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866182 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGAGCT | 5336 |
| rs112707234 | snp | C/T | 0.0178638 | 0.092805 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891454 | TGATGATTCGGTCTT[C/T]GTGTTTGACTCTTTT | 5336 |
| rs112714222 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851210 | TAGACTCTTGTGGAC[C/G]TGGCAAAAATAGTAC | 5336 |
| rs112720754 | in-del | -/TCTC | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844936 | AGACACCATGTTCTT[-/TCTC]TCTTTTTTTCTGAGA | 5336 |
| rs112743678 | snp | C/T | 0.0437281 | 0.141251 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960128 | TCCTGGTGCTACAAC[C/T]GGAATCCACCATGAG | 5336 |
| rs112761099 | in-del | -/A | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814700 | ACTCTGTCTCAAAAG[-/A]AAAAAAAAAGACACC | 5336 |
| rs112763388 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838101 | CTTTTTTTTTTGAGG[C/T]GGAGTCTGGCTCTGT | 5336 |
| rs112772117 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942693 | TTCTGAGCACTTTGA[A/G]GCCGAGAGACTATGA | 5336 |
| rs112777423 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958701 | CAGAGAGACCAGAGC[C/T]GTGCTGCAGGGGCAG | 5336 |
| rs112781068 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901929 | TATTCTGAGAAAAGG[G/T]TCTGTAGCTTTCCCC | 5336 |
| rs112787227 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778743 | CAGCGCAGCCTCAAC[G/T]AGGGCTTCAAATTAG | 5336 |
| rs112797817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955750 | CCAACGAAAGTCCCA[C/T]GGATGCGTCTAGTTG | 5336 |
| rs112804572 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881911 | CCTGCCTTGGCCTCC[C/T]GAAGTGCTGGGATTA | 5336 |
| rs112806963 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844974 | TTGCTCTCTTGCCAG[C/G]CTGGTGTGCAGAGTT | 5336 |
| rs112828651 | snp | C/T | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923160 | TGTGTCACTACAATA[C/T]AGGGTCACTCCCACC | 5336 |
| rs112833318 | snp | A/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927416 | GCTTGGAAGGATTTC[A/T]TTATGCAGGAGAATT | 5336 |
| rs112847188 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907310 | TTCATCGGGGGAAAA[A/T]AAAAAGAAGTCATTA | 5336 |
| rs112866202 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849693 | GGAGAATCACTTGAA[C/T]CCAGGAGGCGGAGGT | 5336 |
| rs112895477 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868031 | CAGCTGAACCTCACT[A/G]TGTGGCTTCGAAGAA | 5336 |
| rs112906428 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882418 | GGCCTCATGTGGCTC[C/T]CACTCCAGAGCACTC | 5336 |
| rs112911514 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873034 | TTTGGGGAAAACATA[G/T]TTCTTAGAGTGGATC | 5336 |
| rs112918501 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959891 | TCAGCTCCTCACTTC[A/C]TTCTACTTTAAAGCC | 5336 |
| rs112920457 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838649 | GCGTTAGGACAAATA[C/T]CTAATGCCTGCAGGG | 5336 |
| rs112920505 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866637 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGAGCT | 5336 |
| rs112924208 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899153 | GAGGTCACGCCATTG[C/T]ACTCCATCCCGGGCA | 5336 |
| rs112927556 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929983 | TGAGCCTCAGTTTTA[C/G]TACTACTAGCTGTAT | 5336 |
| rs112942016 | snp | A/G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822710 | TGTAGTGAGTGAACC[A/G/T]AGTTCATGCCGCTGC | 5336 |
| rs112947035 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863857 | CAGGAGGTGGCAAAG[C/G]GTGAGGGGGTTGCAG | 5336 |
| rs112961627 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844400 | GGCTCACTGCAACCT[C/T]TGCACCCCCACAATG | 5336 |
| rs112976324 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880415 | AAAAACTGGCACAAG[G/T]GGGCAAAGATAGAGA | 5336 |
| rs112987269 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811230 | TCAGTGTCTGCATCT[A/G]TCAAATGGGCACACC | 5336 |
| rs112990942 | in-del | -/AT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830647 | AAAAAAATGTGTGGG[-/AT]GTGTGTGTGTGTGTG | 5336 |
| rs113009181 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905183 | TGAGCCACTGCGCCT[A/G]ACCAGTATGGGCAAT | 5336 |
| rs113013805 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803659 | CCTCCCTCCCTCCCT[C/T]CCTCCCTTCCTTCCT | 5336 |
| rs113029658 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820509 | TAGTTTTTCCTTTTC[C/T]GTTGCTGAGCAGCAT | 5336 |
| rs113030180 | in-del | -/GAATTGTATTTG | 0.438105 | 0.164671 | cds-indel | PLCG2 | GRCh38.p7 | 16:81962193 | GGGCCACTAAGTGAT[-/GAATTGTATTTG]GAAGCAAAAAGGATG | 5336 |
| rs113035491 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780376 | AATCGGGGCGCATCC[A/C]TGGAGAGTCCTTGGG | 5336 |
| rs113050796 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888847 | TTTATAAACAAAATA[C/T]TGTTGGAATACAACC | 5336 |
| rs113056453 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861345 | CTTGAAGGTGACTTC[A/G]TGTCTGGTCAGTGTC | 5336 |
| rs113073324 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929894 | TTGTATCATCTTCCC[C/T]CATCCCTGTATCTGC | 5336 |
| rs113086658 | snp | C/T | 0.274124 | 0.248833 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899289 | ATATATATATATATA[C/T]ACACACACACACACA | 5336 |
| rs113088759 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877662 | GCTGCTGGTGGCTGC[A/C]AGCAGTCCTACAAGT | 5336 |
| rs113092547 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893614 | CTTTGGCGGCTCGGG[C/T]GGAGAAGTTCCCCCA | 5336 |
| rs113094259 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887627 | TCACCACCTGATTTG[C/T]GTCTGTTCTTCTATT | 5336 |
| rs113104341 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848406 | TTGGAAGGGGGTGTG[C/T]GGATGTGCAGGGCTG | 5336 |
| rs113109566 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824395 | CACCTCAACCTCCCA[A/G]AGTGCTGGGATTACA | 5336 |
| rs113123633 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929704 | CCCAGCCTGCTTTCC[A/G]CATTTATAACCTGCT | 5336 |
| rs113134249 | in-del | -/GTAATCCCAGCACTTTCGGAGGCTGAGGCGG | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898927 | CAGTGGCTCACGCCT[lengthTooLong]GTGGATCAACTGAAT | 5336 |
| rs113141646 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877869 | TGTCATTGCATCGCT[C/G]CTTGGCTTGTAGATG | 5336 |
| rs113142862 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792727 | CAGCCCTCATGAGAA[C/T]TTACTCACTATCACG | 5336 |
| rs113148922 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838802 | ATATATATATATATA[A/T]ATATATGTAAATAAC | 5336 |
| rs113151559 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844701 | TGGATTGTGCATTTT[C/G]CATAAAAAAAGAGTT | 5336 |
| rs113181624 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866678 | ACCAGCGTGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs113191536 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939314 | ATCTTAGCCCCTAGA[C/G]GGCAGGAGGGACAAG | 5336 |
| rs113192250 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874071 | GTTGACCCCTGGTGG[C/T]CAGAATGCCACATTG | 5336 |
| rs113206957 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842557 | GTCTGTCTGTTTGCT[C/T]GCTTGAATATGTCTT | 5336 |
| rs113211084 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778599 | ACGGGACATCAATTG[C/T]CTGGGGTTCTTTGCT | 5336 |
| rs113221518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824660 | GTTATAATTAAAGGG[C/G]AACACTGAGGCCAGG | 5336 |
| rs113237525 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876844 | AATTAACTGCTGCCT[C/T]CACGGTGCACCCGTA | 5336 |
| rs113237990 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953503 | TATTTTTCCCCCCAA[C/G]AAACAGGAGAAAAAC | 5336 |
| rs113242386 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855905 | AGTTGGTAGAGATGG[A/G]GTAGGAGGGCAAGGC | 5336 |
| rs113252062 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920644 | GCCACATCACAAGCC[C/G]TAAGGTGACATGAGG | 5336 |
| rs113252891 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877998 | TTTTTTTTTTTTTTT[C/T]TGAGAGGGAGTCTCG | 5336 |
| rs113268178 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866394 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs113282708 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866539 | GCTCCCAGGATGAGC[A/T]CCACTGGGGCACCAG | 5336 |
| rs113298118 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878946 | GCCAATGAGCTTCCG[A/G]TTGCTTCAACAAGCA | 5336 |
| rs113312393 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902731 | CCATTCTCACACTGC[G/T]CATAAAGACATACCC | 5336 |
| rs113312523 | snp | C/T | 0.00810922 | 0.0631574 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908398 | CTTTCAGAAACCCCT[C/T]CTCTCTTTGCGGCCC | 5336 |
| rs113313312 | in-del | -/AGAT | 0.294138 | 0.248177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940715 | CTTCCTACACAGCTG[-/AGAT]GAGATAGACACTTCC | 5336 |
| rs113371178 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917078 | CCCGGACCCTGGTAA[C/T]CACCATTCTACTCTC | 5336 |
| rs113376523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944519 | TGAGGCTGAAATTCA[G/T]TGTTGTGTGATCATA | 5336 |
| rs113395256 | snp | A/G | 0.0376841 | 0.13244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916497 | AAGTTGTTTATATGT[A/G]TCATGTACAACATGG | 5336 |
| rs113395397 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908685 | CAGGCAGGAATTGGG[C/T]AGGCTGGGACCTGAA | 5336 |
| rs113395699 | in-del | -/C | 0 | 0 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960400 | GCAGCACTGATAGAT[-/C]AAAACCACCACTGCA | 5336 |
| rs113395854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874619 | AGCTGGATTTCTCAG[C/G]CTCCTGCAGGAGACA | 5336 |
| rs113396778 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879444 | AACCTTTTGGTGGGA[C/G]CTACTCCTTTGAGAT | 5336 |
| rs113397265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894232 | CCAAGAGTTTGAGAC[A/C]AGCCTGGGCGACATG | 5336 |
| rs113403496 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860516 | AAGAGGGCACCCTTT[C/G]CTGATGATTTATTGT | 5336 |
| rs113426328 | snp | C/T | 0.444444 | 0.157135 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910340 | AGGTGATCCACCCGT[C/T]TCGGCCTCCCAAAGT | 5336 |
| rs113426730 | snp | A/C/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952581 | AACCAACCAGGGAGC[A/C/G]CTCCCAATGGCCACA | 5336 |
| rs113445158 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892024 | GCCATGTCCTCATGT[A/G]CTGGGAGGAAGACCT | 5336 |
| rs113482985 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886538 | GGCAGCATTTTTAAT[A/G]GGAATGAAAACTTGG | 5336 |
| rs113485652 | snp | C/G | 0.469544 | 0.119585 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803641 | TTTCTTCTTCCCTCC[C/G]TCCCTCCCTCCCTCC | 5336 |
| rs113495987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826923 | TCCCTGCTGGAGATC[C/T]GCAGAACCAGCCTCC | 5336 |
| rs113500704 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856006 | TTAATTTGGTAAGGA[C/G]ACCAGAAGAACCCGG | 5336 |
| rs113512081 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803663 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 5336 |
| rs113513343 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940436 | GTGAGAGGGTGGCAA[-/G]GGGAGAGACCTTTGG | 5336 |
| rs113521610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828813 | ACATAGAAGGTTTCA[A/G]CAAATGTGAATTTAT | 5336 |
| rs113523554 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922862 | AAGAAAATTTCTAAC[C/G]AAGGAAGTTCTATCT | 5336 |
| rs113523732 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866385 | CACTGGGGCACCAGC[A/G]TGAGAGGACGCTGGC | 5336 |
| rs113525853 | snp | C/G | 0.0197687 | 0.0974348 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960032 | GCTGCTGTGTAAAAT[C/G]CATGCGTGGCCAAAG | 5336 |
| rs113528092 | snp | A/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929594 | AGAGCTAGGGTTTCG[A/C]CATGTGGGCCAGGCT | 5336 |
| rs113528192 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939346 | GGAATGCTTGCTCTT[C/G]CAGGAAAAGCCAGGA | 5336 |
| rs113529789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866328 | CACTGGGGCACCAGC[A/G]TGAGAGGACGCTGGC | 5336 |
| rs113533948 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785529 | TTCTTAATTTTGCTC[A/T]GGAATAAAGAGATGG | 5336 |
| rs113539756 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878209 | CAGGATGGTCTCCAT[A/C]TCCTGACCTAGTGAT | 5336 |
| rs113562683 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844599 | ATCGCTGGGATTACC[A/G]GCGTGAGCCACTGTG | 5336 |
| rs113584400 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954971 | ACAGTGTAAAAGTGT[G/T]CCTATTTCTCCACAG | 5336 |
| rs113601134 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783441 | CTATCTGTGTGACCT[C/T]GGATAAGTCCCTTAA | 5336 |
| rs113650383 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844954 | TTTTTTTCTGAGACA[A/G]GGTCTTGCTCTCTTG | 5336 |
| rs113652744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948247 | TTCTCCTAAGTTGTC[A/G]TATTATATCCCATCT | 5336 |
| rs113675336 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812429 | ttgatttgcatttct[C/G]taatgaccagtgatg | 5336 |
| rs113678037 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936068 | AAGAGGGAGATTCCT[C/G]GTTTCCTTTTATAAT | 5336 |
| rs113699477 | snp | C/T | 0.294576 | 0.245994 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800511 | GAGGATGATGGCTTC[C/T]AGCTTCATCTATGTC | 5336 |
| rs113713074 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865848 | TCCCTTGCTCCCAGG[G/T]TGAGCTCCAACTGGG | 5336 |
| rs113725270 | in-del | -/A | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896582 | ACCCTGTCTCAAAGG[-/A]AAAAAAACCCAAAAA | 5336 |
| rs113736942 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843803 | CTTGTCAGAAGCAAA[C/T]GCTGGGATGAAAGAA | 5336 |
| rs113750593 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928794 | CAGTGAGTATGATGC[C/T]ATGTCTGCTATTAAT | 5336 |
| rs113751215 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885053 | CCACCATGCCTGACA[A/G]TTTTTTTTTTTTTTT | 5336 |
| rs113755819 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889847 | ATTTTTAGTAGACAG[C/G]GTTTCACTATGTTGG | 5336 |
| rs113758309 | snp | A/C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849771 | AGCAAAACTCTGTCT[A/C/G]AAAAAAAAAAAAAAA | 5336 |
| rs113818298 | in-del | -/GG | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905858 | GAGATGGGATTTAGT[-/GG]CGTGTTGCCCAGGGT | 5336 |
| rs113818545 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942675 | TTATCTTTGGTTTTA[A/T]AATTCTGAGCACTTT | 5336 |
| rs113819045 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933272 | GTTGACGGAGTTCCC[A/G]CACTGGGCACAGCTA | 5336 |
| rs113847096 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790556 | CTCTGGCAATTTCCT[C/G]ACGGGGTTCTGGTTA | 5336 |
| rs113851485 | in-del | -/AAG | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860227 | ATTTTTTTTTAAAAA[-/AAG]CAAACGCAGTTTTGG | 5336 |
| rs113857166 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876219 | TTGTAGAGACAGTTT[C/T]ACCATGTTACCCAGG | 5336 |
| rs113862797 | snp | C/G | 0.162253 | 0.234095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780854 | CAACATGGTGAAACC[C/G]CATCTCTACTAAAAC | 5336 |
| rs113870293 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886089 | CAGTTTAGTAGGGAA[C/T]GATTAAAGTTAAATT | 5336 |
| rs113870915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851384 | TCCGTTTTCTTGTTA[C/T]TTTGCATTTGTTTTG | 5336 |
| rs113877492 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945184 | TATTGTTTGAAGGTG[A/G]TAAAGCAACTGAGAG | 5336 |
| rs113879948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850700 | GATATTTAAGCATGT[A/G]GAAGCGGGGAACTTC | 5336 |
| rs113888605 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953102 | CAGACAAAAGTTGCT[C/G]GACATTCATACAAAA | 5336 |
| rs113889084 | snp | C/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943042 | ATGTCTCCGATTTAA[C/G]AGGCACACGCCTAGT | 5336 |
| rs113898194 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904655 | TGGGCACAGGTGGTG[G/T]TGTTGTTTATTCACC | 5336 |
| rs113911917 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814479 | GGGCAGATCACATGA[C/G]GTCAGGAGTTCGAGA | 5336 |
| rs113912293 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894382 | TGTGGTGAGCTGTGA[C/T]TGTGCCACTGCACTC | 5336 |
| rs113924235 | snp | A/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858868 | AGCTTTTTGGGGATT[A/T]AATGACTATCATCAG | 5336 |
| rs113931977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860268 | TAGATTAATGCATTG[C/T]CATTTCGGAAATCAT | 5336 |
| rs113937963 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901154 | ATCCTCTCTCGGAGA[C/T]AGCCCCATGCGAGGT | 5336 |
| rs113939998 | snp | G/T | 0.444444 | 0.157135 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854885 | AGCTGAATAAGTGAT[G/T]ATTAGATAGTTTTAA | 5336 |
| rs113950536 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838799 | TATATATATATATAT[A/G]TATATATATGTAAAT | 5336 |
| rs113963924 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813604 | GAGCTTAAAACAACA[A/C]TTCTGTGGGTCAGGA | 5336 |
| rs113970793 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819182 | CATGGAAGACAAAGA[-/C]CTTGTTGGGTGCCGG | 5336 |
| rs113973665 | snp | A/T | 0.184521 | 0.241273 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828265 | TTTTTTTTTTTTTTG[A/T]GACAGAATCTTGCTC | 5336 |
| rs113976297 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933166 | GTCTGCATTCCTCTC[G/T]AACTGGTTTTTATAT | 5336 |
| rs113983451 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837549 | AGGGACCCCCGTGTC[A/G]TGGGTGCCATGGCAA | 5336 |
| rs113984824 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866625 | GCATGAGAGGATGCT[A/G]GCCTCTCCCTTGCTC | 5336 |
| rs113986803 | snp | A/G | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788768 | TCTCTTGTGGCACAG[A/G]GCCAGAGCCCTGCTT | 5336 |
| rs114013114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904545 | GTTTGCACCCCGGTC[A/G]CCTTAGTCTAATCCC | 5336 |
| rs114041507 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944365 | CTTAATACAGTATAA[C/T]GATTATTTACACAGT | 5336 |
| rs114049140 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923872 | GAAGTCTTTCTAAGT[G/T]GCAAGCAGTCTGCTA | 5336 |
| rs114050040 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807550 | TATGTTTATGTACCT[C/G]TTACAGCTCTAAGAG | 5336 |
| rs114050826 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944024 | CAATGAAGGCATCCA[A/C]GGAATTCAGTAAGAT | 5336 |
| rs114074422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888507 | GGGTCTGAGCACTTT[C/T]TGTGCACCAGGTGCT | 5336 |
| rs114097832 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825416 | GCTTCAGCTTCCCAA[A/G]TAGCTGGGACTACAG | 5336 |
| rs114109221 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897381 | ATCCTATGCTTCAAT[C/G/T]TCCATGTTAAAAAAT | 5336 |
| rs114117465 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922019 | TGAAGGATGTTTTGG[C/T]GATGAGAACAGTCAC | 5336 |
| rs114140686 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856535 | CTGTCCCTCTGTGCC[A/G]TCTTGATTAGAAGCA | 5336 |
| rs114143389 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805594 | CCAATTAAAAAGTGG[A/G]CGAAAGATCTGAACA | 5336 |
| rs114147336 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817410 | ATATTACTATTATTA[C/T]TTTTGAGAAGGAGTT | 5336 |
| rs114173548 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819631 | GCTCTTTCGCCCAGG[C/G]TGTAGTGCGGTGGCG | 5336 |
| rs114180406 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952519 | TAACATTTCAGTAAA[C/T]AAAGAAGTGCTGAAA | 5336 |
| rs114194996 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883416 | TCTCACCCTTCTGCC[A/G]CCTGTGCTCACCTGG | 5336 |
| rs114200362 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928482 | GTATCTCTGCTAAAC[A/G]GTGTGCTTTGGAAAC | 5336 |
| rs114215669 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785927 | ATCAGTTCACTCTTT[A/C]ATTCTGCCCTTTCAG | 5336 |
| rs114219889 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820526 | TTGCTGAGCAGCATT[C/T]CAGTGACCGAATATA | 5336 |
| rs114229093 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870196 | GATTGCTACACAGTT[A/G]CCATTTAATTCTTTA | 5336 |
| rs114262189 | snp | C/G | 0.00533497 | 0.0513714 | missense | PLCG2 | GRCh38.p7 | 16:81937830 | TTCTGCAGCCTGAGA[C/G]CATGAGGACAGAGAA | 5336 |
| rs114277798 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793803 | AAGGGGGAGCTATCC[C/G]TGCTTTATTCATAAA | 5336 |
| rs114305682 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877651 | GACACCGCCTGGCTG[C/T]TGGTGGCTGCCAGCA | 5336 |
| rs114327983 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950731 | ACAATTTGAAGATAA[C/T]AATTTTCTAAATATA | 5336 |
| rs114332311 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798642 | AGGCCAGGGGTAGGC[A/G]TGAGTTTTGGGAGGT | 5336 |
| rs114336903 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898061 | AGCTGGTATTAACAG[A/G]CACTGTGCAGTGGCA | 5336 |
| rs114356439 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924732 | ATCAAAGATGCAGCC[A/G]AGTTACCCATTGAGC | 5336 |
| rs114361686 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914894 | CAGTGTTTCTCAAAG[A/G]GTTGGGGTGTGAGGA | 5336 |
| rs114403976 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799956 | CAGACCCCACATACT[C/G]AAGAGCAAGGGATCC | 5336 |
| rs114413745 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815465 | CTGAGAGACCACCCC[C/T]TAGAGGCTTCCTCAT | 5336 |
| rs114446251 | snp | G/T | 0.00507745 | 0.0501293 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956912 | CCTGCAAAAACTTTT[G/T]GGGGGTCTCTAGGCA | 5336 |
| rs114459690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926145 | AAGCTAGGCAGCATG[C/G]CAGGGGCATGATAGG | 5336 |
| rs114466443 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816504 | TTTTTTTGAGACACG[G/T]TCTCATTCTGTTGCC | 5336 |
| rs114472783 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839460 | GCCTATTAAAATATT[A/C]ATAGGCTGTATATAA | 5336 |
| rs114484047 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929228 | CTGCTTTGAAGTGGG[C/T]GTGGTGCAGCTCCCA | 5336 |
| rs114496028 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951991 | TTGTATTTATTGAAC[C/G]TAACCACTTCTGTCT | 5336 |
| rs114501233 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861968 | GTGCTCACCGGCTTC[C/T]TCTCCTCTACCTCCC | 5336 |
| rs114501579 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894947 | GGCTCCAGTGTTACC[A/G]AAACGACTCATCATG | 5336 |
| rs114516822 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883763 | TCAAGCCTGCCAGGT[C/T]CCCTGGGAGATAAAC | 5336 |
| rs114530774 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915543 | ATTCTCTTTTCTCCC[A/G]GGGAAGTTAGTTGTG | 5336 |
| rs114570910 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922781 | AGCTTTTCCCACTAA[C/T]ATTTGCTTGCCGTGT | 5336 |
| rs114579320 | snp | C/T | 0.01442 | 0.0836782 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893667 | GCCCCCCAACCCCTG[C/T]GGCTGCCACTCTCAC | 5336 |
| rs114594161 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845324 | TACATCTTTGTTTTT[C/T]TTCCCCTACATTTTT | 5336 |
| rs114601418 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921049 | AGCTTCTTCCTGTGT[C/T]TACTCATGGGCCAAA | 5336 |
| rs114618894 | snp | C/T | 0.00262972 | 0.0361655 | missense | PLCG2 | GRCh38.p7 | 16:81928585 | AATCCCTTAGGGTCT[C/T]TTTGCAGAGGAATAT | 5336 |
| rs114620875 | snp | A/G/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920843 | TGTTGATGTGCTGTC[A/G/T]TTGAACCTGGAACGT | 5336 |
| rs114623928 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805953 | TCATGTGTGTAGTTT[A/G]AAGTTTTCTAGTTGC | 5336 |
| rs114641154 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901553 | CCCCGAAGAATCCAC[G/T]GTTAGAATCAGAGGG | 5336 |
| rs114642466 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909059 | CTTGTGCATTCATTC[A/T]TCCACCCACTTATCC | 5336 |
| rs114651604 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921977 | AATGCATTAAGAGAC[C/G]TTAGTAGCAAAAACT | 5336 |
| rs114660464 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872098 | CTTTGGGAGCCCAGG[C/T]GGGTGGATCATTTGA | 5336 |
| rs114663482 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930805 | TGTAAAAGATTATAT[C/G]TAACAACATAGAAAA | 5336 |
| rs114663707 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797256 | GAGGGATCTAGTTAA[A/C]GATGTCCCTTGGTGA | 5336 |
| rs114674757 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818016 | ACCTGGTTGTCATCT[A/G]CTCTCTGTTCCTTCC | 5336 |
| rs114688616 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839868 | CCAGCCTAGGCAACA[C/T]AGTGAGACCTTGTCT | 5336 |
| rs114718283 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861651 | CTGGTCTCTTTCAGC[C/G]TCGGAGGTGATGCCT | 5336 |
| rs114741216 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793866 | CCCAAGTTAAGGAAA[A/G]GGCAGAGCTACAATT | 5336 |
| rs114751436 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795921 | GTGCAAGGGATGCTG[C/G]GAAACATGCCCTAGC | 5336 |
| rs114754914 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944858 | AGTCCCCCATAGATA[C/T]CAAGGGCCAACTGTA | 5336 |
| rs114780818 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922397 | TACCTGTTATGGTTG[C/T]TTAAGGATTAAAGGA | 5336 |
| rs114798296 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874872 | ACCTCTAACTAGGCT[A/G]TAATAACAGTATCAT | 5336 |
| rs114813422 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888139 | AATAAATGACTTGCG[C/G]AGTTGTGTGGACTAA | 5336 |
| rs114834283 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798909 | AGGTGTCTCTCTCCC[C/T]AGCACTACCAGCCAC | 5336 |
| rs114836755 | snp | G/T | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840812 | AGGCAGCTCCCTTCC[G/T]AGTGGCAAGGAACAG | 5336 |
| rs114845770 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785148 | GGTCGTGAGAGAGTC[C/T]ACGCAAGGATTCCTC | 5336 |
| rs114849889 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942177 | CTTGGTTACCCCGAC[A/G]TCCTCTTGAAGGATG | 5336 |
| rs114853677 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782538 | TGAGCTGGGTGCTGG[C/T]AGGATTTGAATGGTG | 5336 |
| rs114882834 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929303 | TGACCCTCCCTGGGC[A/G]GGCACGGGCATGCTC | 5336 |
| rs114919903 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898571 | ATTTGCCTTCATTTC[G/T]ATTGAGTGACGTGAT | 5336 |
| rs114921598 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851931 | TTAATTGTCTGCTCT[A/C/T]CTCCTCTAGCTCCCA | 5336 |
| rs114926434 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858133 | AAAGGGGATGCTTTC[C/T]TTGCCTTCTGCAAAA | 5336 |
| rs114945346 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793823 | TTATTCATAAAGAGA[C/T]TGAGTCTTGGGGAGA | 5336 |
| rs114951604 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946037 | GACCTCTGGCTTCCA[C/G]AAAGTCAGCCCCCAG | 5336 |
| rs114952272 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937079 | GGTGGGTCAAACAGC[A/G]CTTGCATTTTGATCA | 5336 |
| rs114956198 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872932 | GCTGGCCACACAGTG[A/T]GGCCACCTGATGGGT | 5336 |
| rs114989552 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804865 | TTCTTGAAAGCTTGG[A/G]AGCAGTATTGAGCAT | 5336 |
| rs114992826 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816301 | GCTTGAACCTGGGAG[A/T]TGGAAGTTACAGTGA | 5336 |
| rs114993267 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894265 | GAGATCGTATCATTA[C/T]GAAAAGTAAAAAAAT | 5336 |
| rs115004789 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791522 | TCACTCACACATCTG[A/G]TACCTTAGTGGTGAT | 5336 |
| rs115021547 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777480 | CAAAGGAATTGCCCC[C/T]AGATGTAGTCATTTT | 5336 |
| rs115031275 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795090 | AAAGAGGACCTGATG[A/T]GTGTTGGGCAATGTG | 5336 |
| rs115066116 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799987 | AGGGTCTGACTGCCT[A/G]GGTTCAGATCTTGGC | 5336 |
| rs115084540 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916602 | TTTTGTGTGTGGTGA[C/G]ACTTAAAGTCTACCC | 5336 |
| rs115100804 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893653 | TGAGGTGCAGGCTTG[C/T]CCCCCAACCCCTGTG | 5336 |
| rs115109778 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901621 | TTTGTTTAACCTGTA[C/T]ATAAAACTTAATACT | 5336 |
| rs115120037 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856475 | TAATAGCAACCATGG[G/T]TATTAGCAAGCCATA | 5336 |
| rs115148168 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792742 | TTTACTCACTATCAC[A/G]AGAACAGCATGGAGG | 5336 |
| rs115154204 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840192 | CAATCAACGAAGGGC[A/G]ATGAGATGGCTGCCT | 5336 |
| rs115163086 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890702 | CCATATGAGGTCGTT[C/G]TCACGCAGCAGAAAT | 5336 |
| rs115168660 | snp | C/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958865 | CTGCTGCTTGAAAGA[C/G]GTAGACAAAAGTTAG | 5336 |
| rs115179082 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855141 | CTTGAACCAGTGAGC[C/G]AAGATTGCATCACTC | 5336 |
| rs115184717 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940341 | GTTTGATTTCATTTT[C/G]AAATATTACATGCGG | 5336 |
| rs115187616 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852176 | TAGACAAGGTGGTCC[C/T]TGCCACTCCCAGGCT | 5336 |
| rs115195639 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866806 | CTCCTCTCCCCACGA[C/T]CCCTCTCGCTGCCGC | 5336 |
| rs115196202 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825586 | AGGCGTGAGCCACCG[C/T]GCCCAGCCCGAGATG | 5336 |
| rs115210011 | snp | A/C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917656 | GCTGAACATTTTTTA[A/C/T]GTAACTGTTGGCCAT | 5336 |
| rs115235883 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898435 | TGTTCTAGTAAGGGT[G/T]TGTGGATCAGGATCG | 5336 |
| rs115250436 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877749 | GCATGTAGGCGTCAT[C/T]GCTTCTTGGCGTGTA | 5336 |
| rs115277251 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920996 | GACAGGGCCTCTCTG[A/C]TTTTGGGTTAGTTTC | 5336 |
| rs115288714 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857037 | ATGCAACCAGTCTAT[G/T]TTAGACTTCTGGCCT | 5336 |
| rs115293846 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928183 | ACAGGACATGGGGAG[C/G]CACAGAAGGTTCTTG | 5336 |
| rs115300321 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928888 | GATATTATTACCAGC[A/G]TCACTCTTATTATTT | 5336 |
| rs115304988 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831513 | TTGTCTCAGTTTTAC[A/C]CCTGGGGACATGGTG | 5336 |
| rs115307706 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852339 | CACTTGGGTCATTCC[C/T]TGGCCCCTGCTGTCG | 5336 |
| rs115311333 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821204 | CCTGGCCACATTACC[C/T]GCTTTATCAGATTGT | 5336 |
| rs115314940 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795793 | CAGCCTTGAACTCCT[C/T]GGATCAAGTGATCCT | 5336 |
| rs115315772 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818127 | CTTTACAGGGCTCTC[A/C/G]TGAGTATTCAGCCAG | 5336 |
| rs115341001 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872916 | GCATGCAGAGCTGTG[G/T]GCTGGCCACACAGTG | 5336 |
| rs115346388 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915172 | AGGCAGGGTGGTGGA[A/G]GGTGAGTAGCTCTCC | 5336 |
| rs115357520 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798750 | AGCAAAATTAGGCAA[A/G]GCATGGTGAGAGCAT | 5336 |
| rs115370742 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888761 | CTTCATACTAACAAA[C/T]GTAAAGAGCTATCAT | 5336 |
| rs115399341 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807604 | TAATTCCACAACTGT[A/G]TGTGTTCAATACGCA | 5336 |
| rs115409391 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807132 | CAGGTGGTCAGTGGA[C/G]ACCTCACAGCAGAGG | 5336 |
| rs115424998 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960618 | TTGTTTTCCAAATTC[A/G]ATCTCAGAATCTTTT | 5336 |
| rs115433450 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856090 | TCCGGAACCCTAAAT[G/T]CAAGGTCAGCACAGT | 5336 |
| rs115443929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890105 | GTAGAGCCATGCGAA[C/T]GCCCGAAAAGACGTC | 5336 |
| rs115472157 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869365 | CTCTCTCATGAAGCC[A/G]TGGCTTGCCTTTGAG | 5336 |
| rs115481801 | snp | C/T | 0.0364509 | 0.129988 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778413 | ACTTGGAAGTGAAAT[C/T]CAAGTGCCTGACAGC | 5336 |
| rs115497977 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931821 | GAGCACCTCTTGTTA[C/G]AGAGAGGCAGGGATA | 5336 |
| rs115502796 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923154 | CAATATTGTGTCACT[A/G]CAATATAGGGTCACT | 5336 |
| rs115504013 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915258 | ACTTCTCCTTGCCCT[C/T]TACATATTTGTAAAG | 5336 |
| rs115524804 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804504 | GATTGGCAAGGATGT[A/G]CTTCTTGGCTTGAGT | 5336 |
| rs115533522 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878908 | AGGGGCCAATTCCTG[C/T]AAACACGTTCCCAGG | 5336 |
| rs115563301 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835035 | ACACTGTTTTTCTCA[A/G]TGGGAGGAGGTGGAG | 5336 |
| rs115570507 | snp | G/T | 0.000465815 | 0.0152542 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889159 | GATCTCTCGTTCTCT[G/T]TGTCATTTTAAGGAG | 5336 |
| rs115583707 | snp | A/G | 0.00615664 | 0.05514 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81927178 | GGAGCTAGAAAAGCA[A/G]GTGAGTCCCCCTCTT | 5336 |
| rs115615361 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961433 | AATTTGGGCTATGTG[C/T]TTATTGATTCAGCTC | 5336 |
| rs115616214 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950687 | ACTGGACTAGATTCA[A/G]AAGACACAAAAAGAT | 5336 |
| rs115630309 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885698 | TTTTTAAATGCCATC[C/T]GATACCCAGCCTGCA | 5336 |
| rs115701969 | snp | C/T | 0.0272675 | 0.113535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923231 | GCCCCAAACCCTAAC[C/T]CCTAACCCCTAACCC | 5336 |
| rs115721445 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813722 | GCCAGGCTGGAAGTT[C/T]CCAGGCAGCTTTCTG | 5336 |
| rs115733596 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948945 | ATGAGAACTGTAACA[C/T]ATAACTCATAGGATC | 5336 |
| rs115733960 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929415 | TATTATTTCTTTTCG[C/T]GATAGAGTCTCGCTG | 5336 |
| rs115738695 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899314 | CACACATAAATATAT[A/G]TGTGTGTATATATAC | 5336 |
| rs115741964 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947214 | TGTGTTGATGCAGAT[G/T]TGACTTCCTTGATGA | 5336 |
| rs115760153 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888164 | GACTAAGTGAGATGA[C/G]CATAGGAGGAAGAAA | 5336 |
| rs115778978 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933957 | CCCTTGGACAGAGCC[C/T]TGATGGGCAGTCAGA | 5336 |
| rs115804613 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903632 | GGATGCTTCCAGCAC[A/G]GTGAAGGCAGGATAA | 5336 |
| rs115811204 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826204 | CGGCCCCTTTGCCAC[C/G]TTCATTTCTGGCATC | 5336 |
| rs115813013 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855607 | ATGGGACCTGGTGCC[A/G]CCTTTAAGAAGCTCT | 5336 |
| rs115816567 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863666 | CTGTTTTCTGTAGCA[C/G]CTACACCTTCCCAAG | 5336 |
| rs115819614 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807897 | GATCTCTCAAGAACT[C/T]ACTGAATATTGCAAG | 5336 |
| rs115820215 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781861 | CATCTCATTTCATGT[C/T]CTTTCCCCCCCCCCC | 5336 |
| rs115840182 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818148 | ATTCAGCCAGCTAGT[C/G]TGTTAAGCTCTTACT | 5336 |
| rs115853660 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886171 | TAGGGAGACTGGGGC[A/G]TGTAGATTTACCCCA | 5336 |
| rs115856729 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888995 | GCAGAGAACATTTGC[A/T]GACCCCTGGCAGAGG | 5336 |
| rs115866157 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867174 | CCGTCTCCAGGGCAG[C/T]GGCTGGGCAGTGACG | 5336 |
| rs115874927 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795663 | AGGTTTCTATGGGCC[A/G]TACCTGAAGTGGATG | 5336 |
| rs115876052 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778121 | TGGCACATGCCTGTG[A/G]TCCCAGTGCTTTGGG | 5336 |
| rs115918588 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934957 | TCAATTATCTCCTAT[C/T]GGGTCCCTCCCATAA | 5336 |
| rs115919016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950315 | AATTTACGATCAGAA[A/G]TACTACAGTGTATTA | 5336 |
| rs115921257 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915109 | AGGTTTGAGCACATA[A/C]GGAAATCAGTGTAGT | 5336 |
| rs115930867 | snp | A/G | 0.00981155 | 0.0693506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880863 | TCCGTTTTTGCATTA[A/G]GTGACTTGTCTAAGG | 5336 |
| rs115934710 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827772 | AAATGTAGGTTGTTA[C/G]TGTGAAATCTCCTCA | 5336 |
| rs115951920 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923204 | TAACCCTAACCCCAG[C/T]GCTAAACCCTAGCCC | 5336 |
| rs115974594 | snp | A/G | 0.00214042 | 0.032644 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938951 | CCTCTGCTTTTAAAC[A/G]TCCGGCCAGTGAATC | 5336 |
| rs115980171 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810286 | CACCGTGCCCAGCCC[A/G]TGCTTCTCTCCTATC | 5336 |
| rs115992929 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835068 | ACCCAAAGAGGAGGA[A/G]GTGGCCTTCCAGGTG | 5336 |
| rs115993119 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850382 | AAAAGTTTCAGTGCA[C/T]GAAAAGGATCTTTCT | 5336 |
| rs116028696 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948703 | GGAGACCTGGAGGGA[C/G]ACAAAGGCCCTCCTT | 5336 |
| rs116033842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942128 | TTCCTCTACTGAACT[C/T]ATCCAGCAGAGAGGG | 5336 |
| rs116044047 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824631 | TGGGAGAGACTGGGC[A/T]TTCAGATTCAGCGGT | 5336 |
| rs116045950 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834772 | CCCAGGACGAGGACA[A/G]TCTCCTTTAACAAAA | 5336 |
| rs116080155 | snp | A/T | 0.0189856 | 0.0955633 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961333 | ATCAATCTACATAGA[A/T]GAAATAATTGTGGAG | 5336 |
| rs116099114 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860286 | TTTCGGAAATCATTT[C/T]CGTGTTGATGCACAG | 5336 |
| rs116111920 | snp | C/T | 0.0189856 | 0.0955633 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778431 | AGTGCCTGACAGCTG[C/T]CTAGGTGCCCCTGAA | 5336 |
| rs116119863 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796088 | GAGTCTTGTAGGAAT[C/G]CAGGAGAATGAACAG | 5336 |
| rs116129264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897791 | CTCAGGTGATCCTCC[C/T]GCCTCAACCTCCCAA | 5336 |
| rs116135775 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933418 | GCCCGCATTGTTACA[C/T]GGTCTGTAGCCACCT | 5336 |
| rs116139566 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894241 | TGAGACCAGCCTGGG[C/T]GACATGGTGAGATCG | 5336 |
| rs116142376 | snp | C/G/T | 0.025641 | 0.110417 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823202 | GATGGATTGTTTTCA[C/G/T]TTCAGCCTAGGGGAG | 5336 |
| rs116149037 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797003 | CTATGGATGGGTTGT[A/G]GTTTGTCATAACGGA | 5336 |
| rs116163115 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882315 | GTGTTCCCTAGTGTT[C/G]CCTACCTGATACCTA | 5336 |
| rs116172443 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866775 | TGGGCTCCACTGGGG[C/T]ACCAGCATGATCTGG | 5336 |
| rs116185162 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946574 | GATGCCTTCCTAGAT[A/C]GACTCATCCTTTCTG | 5336 |
| rs116225262 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845915 | AATGCTGGCTCTTGC[A/G]CTTGTGGCTGGTGAC | 5336 |
| rs116232604 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804164 | ACCATTTACTTTCCC[A/G]CCAGCAATGTATGAG | 5336 |
| rs116243104 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922613 | TTATATCATTATTCA[A/G]GGGCAGAGCAATGAT | 5336 |
| rs116245982 | snp | A/G/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902035 | GTCTCAGGCACATCC[A/G/T]AGTTCCAGCTCAGAG | 5336 |
| rs116254974 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867469 | GCTAGCACAGATAAG[A/G]TACCAAACTGATCGG | 5336 |
| rs116255838 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882751 | CCCACCTCATTCTTG[C/T]TCACCCCACCTCATT | 5336 |
| rs116282799 | snp | C/T | 0.00614921 | 0.0551071 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927066 | CAGCGCCCCCATGTC[C/T]TCTCTTCTTATCCAG | 5336 |
| rs116284182 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904594 | CCTGCCCAGCCTGTT[A/C]CCTCTGGACTGCGGC | 5336 |
| rs116285170 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821182 | CAGGCGTGCGTGAGC[C/T]GCCGTGCCTGGCCAC | 5336 |
| rs116292999 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780303 | TACTGGAGCCACCCA[A/G]TTTTCCAGGGCTGTG | 5336 |
| rs116300654 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915142 | TTTGTGATGAGTGCT[A/C]CAAAGGGATTGGTCA | 5336 |
| rs116308929 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860351 | TAATGCTGCTGTGGA[A/C]ACCTTTGGGTCTATC | 5336 |
| rs116336167 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868422 | ACTTACTCTGCATCC[C/T]TCTTGTCTCTTCACA | 5336 |
| rs116356173 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927824 | AAGAGACTGGCAGAA[G/T]AGAGGTGCAAGTGGG | 5336 |
| rs116392731 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961418 | TTAATAATTTAGTGA[A/C]ATTTGGGCTATGTGT | 5336 |
| rs116398362 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830984 | CTTGCTCTTCCTACA[A/G]CCAACCATACACATT | 5336 |
| rs116405351 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807851 | AGCAAGAGAGAGAGG[C/G]AGGGAGGTGCCACAT | 5336 |
| rs116458694 | snp | A/C/G | 0.00557734 | 0.0525397 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800074 | CATCTGTAAAATAGG[A/C/G]TAATAATGGTACCTA | 5336 |
| rs116461035 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798493 | TGGAGAAGGAGCGTC[A/G]ACAGGGTGAAGGTGA | 5336 |
| rs116466123 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959099 | ATATGGCTTTTTAAA[A/G]GAGAGGAGAGTGCTG | 5336 |
| rs116469255 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792719 | AAAACTATCAGCCCT[C/G]ATGAGAATTTACTCA | 5336 |
| rs116481318 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877685 | CTACAAGTGTTCCTC[A/G]GTGTGTAGATGGCAT | 5336 |
| rs116482675 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880218 | TGCACTCCAGCCTGG[A/G]TAACAGTGAGACCCC | 5336 |
| rs116489563 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809746 | CTGATTGGCTAGCCT[C/T]GTCACTTCTGTCCTG | 5336 |
| rs116511355 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888901 | CTGTGGCTGCTTTTG[C/T]AACACAACAGCGGAG | 5336 |
| rs116536188 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862368 | TTTGCAGCCGTGGCT[A/G]TAATAAGCACTTTAC | 5336 |
| rs116566744 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902538 | GGAGATATCTTTGGC[C/T]TCTTTTATAAGGGCA | 5336 |
| rs116568878 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831595 | CTGGGTCTCTGACCA[G/T]TGCTGGGAAAGAGGG | 5336 |
| rs116592478 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873517 | CCAGGATTGAGAAAA[A/G]CTCGATTTACTCAAG | 5336 |
| rs116593049 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890436 | ATCAGATCTGTTTCA[C/G/T]TGTCATAATTTTCTT | 5336 |
| rs116604613 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796653 | ATAATGGAATAGAGT[A/G]GGCCCTAATCCAATA | 5336 |
| rs116640858 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823564 | AGGATCTGGCTCTGT[C/T]GCCCAGGCTGGAGGG | 5336 |
| rs116642266 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808844 | GTGGGCCTGGCCTCT[A/G]TTTCCCCCTATGCAA | 5336 |
| rs116648068 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901473 | GGTGACTCAGGGACC[C/T]GGGGCCCCCGCATTC | 5336 |
| rs116655788 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866819 | GACCCCTCTCGCTGC[C/T]GCTCTGGTAGCGCCT | 5336 |
| rs116661544 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851496 | TTTTTTTACTCTTTT[C/T]ACATGGCCTTTTTGT | 5336 |
| rs116662042 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833322 | ACTGGGGCCTTCTTT[C/T]GCAATCTGTCCACAC | 5336 |
| rs116674073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888397 | AAGAAAAAAAAAATG[C/T]TTGTATTTTAGTAGA | 5336 |
| rs116689594 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819522 | CCTGCCCTGAGGTGT[A/G]AGATCTTCCCAGCCA | 5336 |
| rs116702733 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897814 | CCTCCCAAAGTGTGG[G/T]GATTATGGGCATGAG | 5336 |
| rs116716982 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825906 | CATAGGGTGTTAGGT[A/G]GATCGTAGAGAAAGA | 5336 |
| rs116723431 | snp | C/G/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945097 | GAGAAATTGGGGAGA[C/G/T]AAAAGGAACAGGTTT | 5336 |
| rs116736370 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924958 | TTCCAGGCACACTGG[C/T]GTTCCCTCACTGGGC | 5336 |
| rs116745495 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852182 | AGGTGGTCCCTGCCA[C/T]TCCCAGGCTCATGTT | 5336 |
| rs116751708 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951041 | CACCCAGCCTGGAAT[A/C]CAGTGGTGTGATCAT | 5336 |
| rs116757850 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893553 | GGATTGTGTATTTCT[G/T]TCCTAGGCCTTAGCT | 5336 |
| rs116758417 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907607 | TAGATGCTGGGGTGA[C/T]GCCCTGCAGGGCTCC | 5336 |
| rs116768284 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798902 | ACCGGCCAGGTGTCT[C/G]TCTCCCCAGCACTAC | 5336 |
| rs116777059 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780503 | TATGCCAGCCTCAAG[C/G]AGTTTCTCTTGCAAA | 5336 |
| rs116786455 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901292 | TTCCCAGCACTGCAG[A/G]GGAGATGGGTGATTA | 5336 |
| rs116793333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936018 | TCCACAGTGATACCA[A/G]TTGGGACAATATCAT | 5336 |
| rs116793633 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918749 | AGACATTTTTAAAAA[C/G]ACCCTCTTGGCTGTA | 5336 |
| rs116798351 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807261 | GGTCAGCTCTGGGAC[A/C]CAAGAAAGGGCAGGG | 5336 |
| rs116799253 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847577 | TTAGGGGTTGTGTGC[C/T]AGAAAATGGGGTTGG | 5336 |
| rs116804054 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785103 | GAGATCCTAGGAGGA[G/T]CCGGTGAAAGGGTGA | 5336 |
| rs116818704 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883069 | TTGAGATTCCGATGT[C/T]AGGGTCCCTCTGAAT | 5336 |
| rs116819605 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871730 | GGTGTATGTTTTGAT[C/G]TGACAGTGGCATCCT | 5336 |
| rs116843078 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789415 | CCTGCCCAGTCTCCC[A/G]AGTAGCTGAGACTAC | 5336 |
| rs116859630 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877517 | GGAGGTTAAAAGTCC[A/G]AAATCCAGGTGTTGG | 5336 |
| rs116866940 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854254 | GGGTGGCAGCAAATG[C/G]CCGGGTAGGGTCTTA | 5336 |
| rs116871589 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930952 | ATTGTTTTAGTAATT[A/T]GTAAAAAATATTTAT | 5336 |
| rs116874097 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875477 | TCTTAATTTTTGAAT[C/G]CTTTGTATTAAAGAA | 5336 |
| rs116906243 | snp | G/T | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892726 | AACTTGTGTCATGGA[G/T]GTTTGCTGTGCAGAT | 5336 |
| rs116941826 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877678 | AGCAGTCCTACAAGT[A/G]TTCCTCGGTGTGTAG | 5336 |
| rs116993118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854737 | TGCCCCTTTCTAGCT[G/T]TGTGTCTTTAGGTGA | 5336 |
| rs117005653 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937962 | CCCTGGGGGCTGGGC[C/T]GATGCTGTCTTGAGA | 5336 |
| rs117044854 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796031 | AGGCAGCTCTAGGTG[A/C]CCCAGTGAAGGCTGA | 5336 |
| rs117077093 | snp | A/G | 0.00135203 | 0.0259651 | missense | PLCG2 | GRCh38.p7 | 16:81923570 | GTGCCCTCATCCACA[A/G]TGTCTCCAAGGAGCC | 5336 |
| rs117077358 | snp | A/C | 0.0126979 | 0.078662 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961544 | AAATAACATAAAAAT[A/C]AAAAATTTATTAGGC | 5336 |
| rs117081674 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892640 | CTAGAAGACAGTTAA[C/G]AAATACAAACTTAAA | 5336 |
| rs117105981 | snp | C/G | 0.0930568 | 0.194599 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832461 | GTGGCATGATCACGG[C/G]TCACTGCAACCTCTG | 5336 |
| rs117128903 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792054 | AGGAATGGCATGCAT[A/G]TCGATGGTAGGCAGG | 5336 |
| rs117130976 | snp | A/C/G/T | 0.00279258 | 0.0372817 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953380 | GAGTCTAGGTGGTTG[A/C/G/T]GGTATGTGAGAACAT | 5336 |
| rs117133150 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834454 | GACCCCAGCTTGCCC[A/C]ACCTGCCTGAGCCTC | 5336 |
| rs117135604 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830209 | TCTGTGGTCCCAGCT[A/T]CTTAGGAGTCTGAGG | 5336 |
| rs117170490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930622 | GCTTTGTGGTGTGCA[C/T]CTGTGGTCTCAGCTA | 5336 |
| rs117188390 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842405 | GACTCGGAGCCGTCT[A/G]AGGGCAGGACTGTGT | 5336 |
| rs117201095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847523 | CTAGGAGCCCCCAGC[C/T]CTACAAAAAGATACT | 5336 |
| rs117206377 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936864 | ATCTATTCATCAGTA[C/G]CCTCCTTTACATTCT | 5336 |
| rs117206583 | snp | A/C | 0.0166418 | 0.0897655 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950208 | CTGCAGTGTTTACAA[A/C]AAGAGGCCTAAAGGC | 5336 |
| rs117233649 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916235 | TACAGGACTTTTTGA[C/T]GAAATCGCTTAAAGC | 5336 |
| rs117238340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889562 | CTTAACTCACTTAGA[A/G]CCAGCTGAATGGGAG | 5336 |
| rs117257099 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930663 | TGAGGTGGGAGGATC[A/G]CATGAACTTGGAAGG | 5336 |
| rs117260449 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819363 | CTGAGGCTTCATCTG[C/G]TACCAACCCTGTGAG | 5336 |
| rs117261090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899520 | GAAATGAGACTCATG[C/T]GATGCACACGTGTTC | 5336 |
| rs117268490 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796910 | GCAGGCCTAACACAC[A/G]AATACACTCTCATGT | 5336 |
| rs117281444 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794196 | GCCTGGAAAAGGGCT[G/T]TTGGGGACAAGGGTG | 5336 |
| rs117282904 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908024 | CCTGATTGGCCTTAG[A/G]TGGAGGCCGGTGCTC | 5336 |
| rs117333528 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823284 | TCTGGTGAGCCCCTG[C/T]GGCCGGGGCAGCTGC | 5336 |
| rs117353962 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862160 | ACCCACGAGACGAAT[C/T]GTGTTTCCTGAAGGA | 5336 |
| rs117353991 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836556 | GACCAGCCTGGTTAA[C/T]ATGGTGAAACGCCAT | 5336 |
| rs117360379 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793313 | TCCTTTCTGAGGGAC[C/T]TAGTTGAGCAGTCTT | 5336 |
| rs117374883 | snp | A/C | 0.0107246 | 0.0724382 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962332 | TCTTCTAACCAACAA[A/C]AAGTTAATAATTAGA | 5336 |
| rs117406804 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892038 | TGCTGGGAGGAAGAC[C/T]TCCATTGAAAGTTAA | 5336 |
| rs117425235 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897792 | TCAGGTGATCCTCCC[A/G]CCTCAACCTCCCAAA | 5336 |
| rs117455719 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848902 | TCATAGCAGGCATTG[A/G]GAGGTTTTCTGAGTT | 5336 |
| rs117465906 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794963 | ATAGCCCTTCTCTTA[A/C/T]GCTGAATAGCTGAGG | 5336 |
| rs117471231 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820277 | TTCCATCGCAGGAGA[A/C/G]AGGGTTCCCTCACTT | 5336 |
| rs117476144 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877181 | ACAGAAGTGTCGGGC[A/G]CGGTGGCTCACGCCT | 5336 |
| rs117477174 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788679 | TTGGTGTCATCCTTA[A/G]TTTGATGTATCCTAT | 5336 |
| rs117490803 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924254 | TTCTGTCTGAGAGCA[A/G]TAAGAACTTGCTCAT | 5336 |
| rs117500363 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785522 | TTTTTTGTTCTTAAT[C/G/T]TTGCTCAGGAATAAA | 5336 |
| rs117503313 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887976 | CAGCCCTGTTTGCCT[A/G]TTCTTTTGAAAAGAG | 5336 |
| rs117525018 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902109 | GCAAGTCAGCTGTCC[C/T]GTCCTTTTCTCTACT | 5336 |
| rs117542781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933102 | TCCTGCCGCGTGAAG[G/T]TTCCTGAAATGAAGC | 5336 |
| rs117585223 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798704 | TGAGAAAGAAGGAAA[C/T]GGGAACTTACTAATT | 5336 |
| rs117594647 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869438 | ACATCTTAGTTCAGA[C/G]AGAGGGATCATGGAC | 5336 |
| rs117595326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843568 | ATTTTTCGCGTGAAT[A/T]CAAAGCATCTACAGC | 5336 |
| rs117599504 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920577 | ATGGAAGATAGCAGT[A/G]AATGGGATCTGGGGA | 5336 |
| rs117621599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902350 | GGAACTGATTTCTCA[C/T]GGTTCTGGAGGCTGG | 5336 |
| rs117623053 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880258 | GAAACCTGGCAGTGA[A/G]GATATAGAAAAAGGT | 5336 |
| rs117631133 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920819 | CTTCCATGGAGGTCA[C/G]TTTCAAGTTGTTGAT | 5336 |
| rs117637926 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794208 | GCTGTTGGGGACAAG[C/G]GTGCCGAAGTGAGAG | 5336 |
| rs117640739 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868860 | CACCCTATACTGGGG[A/T]TCTCCAGTGTAGGTG | 5336 |
| rs117654182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882386 | TAATTTTGCCCTGAT[G/T]GCCTGGAGTCTGGTG | 5336 |
| rs117654596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880217 | CTGCACTCCAGCCTG[A/G]GTAACAGTGAGACCC | 5336 |
| rs117660518 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838855 | ATGGTGCATGTAAGG[C/G]TCAAGGCTTTAAGCA | 5336 |
| rs117675832 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943123 | ACCTGATAGCCTCCC[A/G]GAATGCCATGGAGCA | 5336 |
| rs117704063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913302 | CATGTTCTTACGGTG[G/T]TAACAGTCTGCTATA | 5336 |
| rs117705563 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851794 | CTGGGATTACAGGCG[G/T]GGGCCACCAGTGCCC | 5336 |
| rs117711114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806078 | CAATATAATTATTAA[C/T]GAGATATTTGATTCT | 5336 |
| rs117723193 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943365 | ACATGGCCAGCAGGA[A/G]GAAAAGAGAGCTAGT | 5336 |
| rs117725296 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902219 | AAGGAGCGAGTGTGA[A/G]TTTTGTTGACATTCC | 5336 |
| rs117742783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848635 | CCCCTGCTCTGCTCA[A/G]TCATCAGTAATTTGA | 5336 |
| rs117750022 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856996 | AGATTCTTCCCCAGA[A/G]CTTTCAGAAGGAATT | 5336 |
| rs117770574 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836242 | AAACTGAGGCCCAGG[C/G]AGGTAAAATGACTCT | 5336 |
| rs117771065 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842191 | TCCAGAACTCCCTAC[A/C]AAGGGAGGCTTTCTC | 5336 |
| rs117824271 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821585 | TCAGTGCTGGCCCTA[C/G]TTGTTGCCTTGTGTG | 5336 |
| rs117832870 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841181 | GGGCAGGCCCACCCC[C/T]TATCTGCAGGCCAAA | 5336 |
| rs117835631 | snp | A/C/T | 0.00206417 | 0.0320606 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81912621 | TGACAGCCTGAGCCG[A/C/T]GGAGAGGCAGAGGAC | 5336 |
| rs117847874 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804920 | GGCACTACAAGCTCA[C/G]ATGTATCCATGTGAT | 5336 |
| rs117859182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914103 | AGGTGTGTTCAGTCC[A/G]CTGCACACGGATTGA | 5336 |
| rs117868352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872750 | AGGTGGCTGTGGTTT[C/T]TGCAGTTAGCTGCAT | 5336 |
| rs117874225 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796650 | ATCATAATGGAATAG[A/T]GTGGGCCCTAATCCA | 5336 |
| rs117901581 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827695 | AGTGCATGTGTGCCT[G/T]GTGTAAAGTGGACAG | 5336 |
| rs117902527 | snp | A/G | 0.039522 | 0.134904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848730 | CGCTGTGTGCCAGCT[A/G]CTCTGATAGGGGTGG | 5336 |
| rs117917414 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838904 | CATTCCTCGGGTCCC[A/G]GTGACCCAGTCCTCT | 5336 |
| rs117949086 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810943 | GAGGCACCAAGGGAG[G/T]TTATGCACCTGAGAA | 5336 |
| rs117950991 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880097 | AGAAAAAATATTAGC[C/T]GGGCATGGTGGCGCA | 5336 |
| rs117952806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920021 | ATGAGCCATGTGGGT[A/G]TGTTCTGGAGGAAGA | 5336 |
| rs117954043 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923744 | CTTCTTAGGAAGGTG[G/T]CTTGGTGCATGCTCT | 5336 |
| rs117959600 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957632 | TAATATGTCTAAATC[C/T]TCTAAGAAAGAATCA | 5336 |
| rs117963709 | snp | A/G | 0.105924 | 0.204309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864760 | CTGGTAAGTGTCACG[A/G]GGCTGCCATCCTTAA | 5336 |
| rs117964717 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872442 | TTTTGTGTGTGTGTG[A/C]TGGAAGGGGTTGGGA | 5336 |
| rs117978715 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817851 | CCAGGCCAGGGTAGG[C/G]AAAAATGAGACAAGC | 5336 |
| rs117979034 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904748 | AGCAAAACAACATCC[C/T]TGCCCTCATGGGGTT | 5336 |
| rs117980239 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828822 | GTTTCAACAAATGTG[A/T]ATTTATTTCCCCTTA | 5336 |
| rs117991680 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783065 | GGAAGGTTAAGTCCA[A/G]GGCCCTCCCAGAGTG | 5336 |
| rs118019082 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905755 | CCTTGACCTCCCAGG[C/T]TCAAGTGATCCTCCC | 5336 |
| rs118020419 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803453 | ATATTTTGTTTATCC[A/G]TTCATCACTTGATGG | 5336 |
| rs118092709 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786726 | CTCCGTTTGATTGGG[A/C]AGCTGGTTCAGATCC | 5336 |
| rs118095029 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953202 | AAGGCAGCACAATGA[C/T]TAAAGGTTCTGTGGG | 5336 |
| rs118097094 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789699 | GGGGCGTATTATTAT[A/G]ATAAGTCCCCCGGAT | 5336 |
| rs118118936 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951348 | TACTGGAAAGGAGAC[A/T]GAACCCCAAATAATA | 5336 |
| rs118188837 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792115 | CCACATGAGCATGTC[A/G]ACTCTGAATCCCAAT | 5336 |
| rs137863303 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900314 | ACTTGAAAAAAAGAT[C/G/T]AGAGACTTTTTTCTG | 5336 |
| rs137875486 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845727 | GTGGGTAGTGGGATC[A/G]TCATTCACCAAGATG | 5336 |
| rs137901349 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827907 | TCCAACCTGATCAAC[A/G]TGGAGAAACCCCGTC | 5336 |
| rs137905951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796104 | CAGGAGAATGAACAG[C/T]CTCATCGCTGGGCTG | 5336 |
| rs137918666 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875670 | ATTTAATACCTGGCT[A/G]CGTGACTGCTACCCT | 5336 |
| rs137923686 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949836 | ACAAAGCAAAGGCAT[C/G]GAAAGGTAAAATAAA | 5336 |
| rs137929451 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879421 | AAAAGGCTAAGTTTG[C/T]GGCTCTTAACCTTTT | 5336 |
| rs137952624 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920037 | TGTTCTGGAGGAAGA[A/G]AGGATAGCATGCGCA | 5336 |
| rs137975710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924238 | GGTTTTGTGGGGTGA[C/T]TTCTGTCTGAGAGCA | 5336 |
| rs137977069 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840256 | GGCCCCTGAGCTGCC[C/T]ACCCTGTCATGGCCT | 5336 |
| rs137980491 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803956 | AGAGTGCTGGGATTA[C/T]AGGTATGAGCCACCG | 5336 |
| rs137983640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863592 | CTGGATCAGTTGCTG[A/G]ATTGCTGTGTATATA | 5336 |
| rs137994706 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809097 | GTGCTAAGCCAGGCC[G/T]GGTCTCTCTGAGCAT | 5336 |
| rs137996063 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857389 | AATGGATTCTTGTTT[A/C]AAATCCTGTATCTTC | 5336 |
| rs137996393 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881187 | GTTCTGTAGAAAAGC[C/T]TGTGTGCCTCAGGGC | 5336 |
| rs137998840 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961713 | AAAAAGATCATAGTA[C/T]CTATCAAATAACTTA | 5336 |
| rs138001996 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901756 | AATAATGTTGTGCTC[A/G]TCATCACTTTGGAAT | 5336 |
| rs138019296 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848740 | CAGCTACTCTGATAG[A/G]GGTGGAGCTCAGTGG | 5336 |
| rs138021178 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823133 | TCACAGGAAAGTGGC[C/T]TCTTGGATGATGGCG | 5336 |
| rs138032952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789056 | GTATAGGGTATTAAC[C/T]ATGGCATGTGTATAC | 5336 |
| rs138040387 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922140 | GCTCTGTTTGCAGGT[C/G]GGGGAGAGAAAGGCA | 5336 |
| rs138059619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816906 | AGGCACCTGGGGCCA[C/G]ATCCGGTTCTGCCTC | 5336 |
| rs138078413 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877690 | AGTGTTCCTCGGTGT[A/G]TAGATGGCATTGCTC | 5336 |
| rs138081910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836181 | CATACCCTAGAGACT[A/G]TCCAAATGACACAGC | 5336 |
| rs138109253 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898883 | AACGTAAATATGTGT[A/G]TAAATGAAATACAAA | 5336 |
| rs138112860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942343 | AAAAAACAAAGGTCA[A/G]AACCTCAAGGGAGAT | 5336 |
| rs138117070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888941 | TGCGACAGACACCGT[A/G]TGGCTCAGAGAGCCC | 5336 |
| rs138128599 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860147 | TGGCTTATTTACTAT[G/T]ATTATTATTATTATT | 5336 |
| rs138143938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819603 | TTATTATTATTTTTT[A/G]AGACCAAGCTTCGCT | 5336 |
| rs138158454 | snp | A/G | 0.0555041 | 0.157071 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912723 | CACCTTCAGGTGGGT[A/G]CGAGGGTGGGAGGCA | 5336 |
| rs138161681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956144 | CTTCATATAAATGGC[A/G]TCGTGTGATTTGTGA | 5336 |
| rs138170755 | snp | A/C | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800685 | ATTATTATTATTATT[A/C]TTATTGTTATTTCCA | 5336 |
| rs138175513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930900 | AAAAATGCCAAGTTG[C/T]TTAGCTATATTTTAA | 5336 |
| rs138188815 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919005 | TTCTGTGAAGGACCA[A/C]AGAGTGAATATTTTA | 5336 |
| rs138190834 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890992 | ACATGGTAAAATTCT[C/G]TCTCTACTAAAAATA | 5336 |
| rs138199457 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892965 | TTCTCCTGCCTCAGC[C/G]TCCCGAGTAGCTGGG | 5336 |
| rs138225792 | snp | C/G | 0.0189856 | 0.0955633 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959109 | TTAAAGGAGAGGAGA[C/G]TGCTGGGTTGGGAAG | 5336 |
| rs138238586 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916518 | TACAACATGGTGTTT[G/T]GAAATATGTATACAT | 5336 |
| rs138248642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818834 | TATTTAGGTAGAATA[C/T]GAATAGGGGGATTTG | 5336 |
| rs138250202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928471 | TTCCACAGGCAGTAT[A/C]TCTGCTAAACGGTGT | 5336 |
| rs138255155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885986 | TTTATTGGGCACAGT[C/T]ACGTTAGGTCTGAGC | 5336 |
| rs138257975 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875621 | CTTTGCAGCAGACAT[C/G]AAGCAGCGTATCAGG | 5336 |
| rs138285572 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953123 | TCATACAAAATAACT[G/T]ACTAGTATTCTTCCA | 5336 |
| rs138287889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829780 | GTCCACTCTCTCCTG[C/G]TGGGCATTTGTGCTG | 5336 |
| rs138302952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871130 | CATGACAGAGCTGTG[A/G]GCAAAATGTAGAGAA | 5336 |
| rs138307047 | in-del | -/CAAGCTTGGGTTGAAAATATT | 0.102726 | 0.202016 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944282 | GTGGACTCAACCAAC[-/CAAGCTTGGGTTGAAAATATT]CAAGCTTGGGTTGAA | 5336 |
| rs138308994 | snp | C/T | 2.52995e-05 | 0.00355656 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938957 | CTTTTAAACGTCCGG[C/T]CAGTGAATCCTTTGT | 5336 |
| rs138330842 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867433 | TGTGGTCATTATGGG[A/C]ACACTGGGTTGGAGT | 5336 |
| rs138333841 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824237 | CTCCCGGCTTCAAGC[A/G]ATTCTCCTCCCTCAG | 5336 |
| rs138350722 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814568 | GGCATGGTGGCATGT[A/G]CCTGTAATCCTAGCT | 5336 |
| rs138358558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947413 | TCACAGGTGCAGCTC[A/G]GCATTTCTGTCCACA | 5336 |
| rs138376432 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912218 | GATTACAGGCGTGAG[C/T]CACTGTGCCCAGGCT | 5336 |
| rs138383369 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855322 | ACACACATGCACTTT[C/G]CTCACTTTACTCAGG | 5336 |
| rs138393877 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849224 | TGACTGTGGGGATAA[C/T]GTACTGCTTTAAGGA | 5336 |
| rs138407047 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813073 | TGCTGTTTTGTTGAC[C/T]ATAGCCTTGTAGTAT | 5336 |
| rs138437425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809897 | ACGTGTGGCTGAGAT[A/G]CATACTGTGTAGCTC | 5336 |
| rs138450037 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819863 | TGCTGGGATTACAGC[C/T]GTGAGCCACTGTGCC | 5336 |
| rs138484935 | snp | C/G/T | 0.0275645 | 0.114116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851175 | AGTGTCTTTAGTTAC[C/G/T]TTTTATTTTGAAATA | 5336 |
| rs138489612 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793962 | AATGATCTCAAAGAC[A/G]TATCAGATCTGTGTG | 5336 |
| rs138504153 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798707 | GAAAGAAGGAAATGG[G/T]AACTTACTAATTTGT | 5336 |
| rs138507881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922316 | TGGTCGATGTGGGGC[A/G]AATTACTTTCTCTCT | 5336 |
| rs138520066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939824 | TCACAGCTGAAGGAT[A/G]CGGAGATTGTCTTAC | 5336 |
| rs138526726 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881761 | GCGATTCTCCTGCCT[C/T]ATCCTCCGAATAGCT | 5336 |
| rs138530681 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906767 | AAGTTGGGCCAGGCG[C/T]GATGGCTCATGCCTA | 5336 |
| rs138555944 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881455 | ACTGTGCCTCATGAT[G/T]TCCCAAGTGGGGAAT | 5336 |
| rs138556273 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924557 | GGCTGAGATTTGAAC[C/T]GCCAGGCCTTTTGAC | 5336 |
| rs138595663 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904212 | CACTGTTGACACTTA[C/G/T]CTTTCACGTTCTTTG | 5336 |
| rs138607110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903873 | CCCCACACCTGATAC[A/G]CTGTGGCCCACTTCT | 5336 |
| rs138608711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802534 | GACCTACCACCTTCT[C/T]TTGATGAGGAACCTA | 5336 |
| rs138619052 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805410 | AGGCTGAGGCAGGAG[A/G]ATGGCGTTAACCCAG | 5336 |
| rs138637229 | snp | C/T | 0.01396 | 0.0823719 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895880 | TACCAAGATCAAGTT[C/T]GACGACGTCGTGCAG | 5336 |
| rs138639901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857283 | TCTCCTGAGCAGCTG[A/G]GGTTGAGAAACTCTG | 5336 |
| rs138647934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901672 | GCAGCAAGCCACTTG[C/T]GGGCTCTGTCACCAG | 5336 |
| rs138648611 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836336 | TTGGCCCACGTGTCA[C/G]CCATGGACTCGTATT | 5336 |
| rs138674506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921931 | AGAAATGAAATCTTG[A/G]AAAGTTGTGGGCAAA | 5336 |
| rs138679084 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902289 | ATTTCAGTCTGTTCC[A/T]GCAGCTATCACAAAA | 5336 |
| rs138683716 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909955 | CAGAGCTGGGATTTG[A/T]ATCCAGGCATCCTGG | 5336 |
| rs138687132 | in-del | -/CTGGCTGGCTTGTCTCTGATTGG | 0.14665 | 0.227637 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907926 | TCTGGGTACCATGTC[-/CTGGCTGGCTTGTCTCTGATTGG]CTGGCTGCCCCAGGT | 5336 |
| rs138696023 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807355 | ACTGAGGAGGATGGG[C/G]TTCTCAGATCCTGGG | 5336 |
| rs138699122 | snp | C/T | 3.34465e-05 | 0.00408927 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81785985 | TCTCCCTGGAGCGGC[C/T]GACAATGTCCACCAC | 5336 |
| rs138722780 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845069 | GAGTAGCTGAGACTA[C/G]CAGTGTGCACCAGCA | 5336 |
| rs138733190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843021 | GGACCTGGGAAGACC[C/T]GAGGTGATGCTGGGA | 5336 |
| rs138733602 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932925 | TGCCCTCCAGTGTCT[C/G]TGATGCCACAGTACA | 5336 |
| rs138735087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868745 | GTATTGAGATTATCT[A/G]GTCATTTGACATCAT | 5336 |
| rs138736461 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814991 | TAAGAAGTTACTTTT[A/C]TTATTATCAGGACTG | 5336 |
| rs138737146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805554 | AAAAAAACCAAAAAC[A/G]AAAGCTCAACAATAA | 5336 |
| rs138743621 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780301 | GATACTGGAGCCACC[A/C]AATTTTCCAGGGCTG | 5336 |
| rs138756210 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816738 | AACTCCTGGGCTAAA[A/C/G]CAGTCCTCGCATTTC | 5336 |
| rs138761791 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879080 | GAGCTCCCTGAGTGG[G/T]GGAATGCGGTGCGGG | 5336 |
| rs138762798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840057 | GCATGACCTTGTCTC[C/T]AAAAAAACTTAAAGA | 5336 |
| rs138766176 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926632 | CTGAGGGAAGCACTC[-/A]ACGTTTATGCATTTT | 5336 |
| rs138810554 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874978 | TTTTTTTTTTTTTTT[A/T]TTTGAGACAGAGTCT | 5336 |
| rs138834146 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959439 | AATACAGTGCCAAGA[C/T]TTGGGGGTGTGGATG | 5336 |
| rs138859004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888718 | AAGTGACCTGGAAGG[C/G]TGATGTAACTACTAT | 5336 |
| rs138860210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906866 | AACATGGCGAATCCC[C/T]GTCTCTATTAAAACT | 5336 |
| rs138871258 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788580 | TCTGTTTCAGCCACA[C/G]GATGTAAAAGTACCT | 5336 |
| rs138887931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950071 | CAAGAGAGTAAAAAT[A/G]ATGTAAAGAATCAGA | 5336 |
| rs138902212 | in-del | -/TT | 0.45843 | 0.138046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892848 | GTGAGGAACATAAAC[-/TT]TTTTTTTTTTTTTTT | 5336 |
| rs138903395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873998 | TCAGAACCCTCTGGG[A/G]TGCCCTAGATTGCCC | 5336 |
| rs138907413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852467 | TTTCAGAAGAAAGGG[A/G]AAGAAGGGACTGGTT | 5336 |
| rs138923790 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860172 | ATTATTATTATTATT[A/T]TTTTTTTTTTTTTTT | 5336 |
| rs138932132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869431 | CCAGAGTACATCTTA[C/G]TTCAGACAGAGGGAT | 5336 |
| rs138940490 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890172 | TATCTGTAGGAGTAA[A/C]TGAGGAAGTTGCTAA | 5336 |
| rs138945368 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846211 | CTGTAAGCCAAGCCA[A/C]TGACTGACTGGCAGG | 5336 |
| rs138960735 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935920 | TAGTTTAAAAAAAAA[A/C]GTAAATTACAGTAAT | 5336 |
| rs138971659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930703 | CAGGGAGCCAAGATC[A/G]CACCACTGCACTTCA | 5336 |
| rs138977751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826611 | CTTCTCTACAATACT[C/G]AGTGCTTCAAATGGT | 5336 |
| rs138980316 | in-del | -/TCTT | 0.330714 | 0.236612 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857637 | GGGAGCTCTAGTCTC[-/TCTT]TCTCTTCTCTAAAAA | 5336 |
| rs138981519 | snp | C/T | 0.00137411 | 0.0261757 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81883290 | TGACAGGCCGGATGC[C/T]TCTGCTGTTTACCTG | 5336 |
| rs138982257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894009 | TCATCTGTATCTCCT[C/T]AGCTTCCTCCTGGGC | 5336 |
| rs138997701 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834823 | CTTCTTGGCCATGAG[A/C]TGAGGAGTTTTTATT | 5336 |
| rs139002906 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893605 | AACTCAGAGCTTTGG[C/T]GGCTCGGGCGGAGAA | 5336 |
| rs139003082 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855526 | CTCATTCATTCTTTT[A/C]CTACATGTCTTTTGA | 5336 |
| rs139016787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870694 | GACTTTTTCCTTTCA[A/G]AAGCCATGACACTGA | 5336 |
| rs139030224 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812015 | TTCCTATTTCTCTAC[A/G]TCCTCTCCAGCATCT | 5336 |
| rs139047795 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897360 | AGTTTGGGCAAAGCA[C/G]TTACCATCCTATGCT | 5336 |
| rs139052577 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876740 | AGGTCCTGGGATGTT[G/T]CCCAGAGTGACATAA | 5336 |
| rs139061512 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961043 | AAAGTGAAAGACTTA[C/T]CAACAGGGCACAAAT | 5336 |
| rs139075792 | in-del | -/TG | 0.0998734 | 0.199905 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832558 | CATGCCCAGCTAATT[-/TG]TGTGTGTGTGTGTGT | 5336 |
| rs139124866 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874520 | TCCCCTAACCTGTTA[A/C/G]CAAATTGTTTACTTC | 5336 |
| rs139133108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831366 | GGACGTGACCATCAT[C/T]GTGAGAATCTGTGGA | 5336 |
| rs139139807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832984 | ATGACAGTAACTGAG[G/T]GAAACAAGTCACGCT | 5336 |
| rs139156476 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894186 | GTAATCCCAGCACTT[C/T]AGGAGGCTGAAGTGG | 5336 |
| rs139157594 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936620 | AAGTGACAGAGGCTG[A/G]GTTAGTCTGGCTTAG | 5336 |
| rs139158169 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798917 | CTCTCCCCAGCACTA[A/C/G]CAGCCACTCCAGGAT | 5336 |
| rs139165099 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782573 | CCAGGGATCTTTTGG[C/T]CGTGAAGATCTGTTT | 5336 |
| rs139186738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856190 | AGCCTCAGTTTCCTC[C/T]GCATCTGTGTGGGAA | 5336 |
| rs139186831 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815639 | CAAGTCCCTCTTCAG[C/T]TGCTGGGAGTCTGAG | 5336 |
| rs139201133 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813510 | TTGTGATTTTTGCAC[A/G]TTGATTTTGTATCCT | 5336 |
| rs139221979 | snp | C/G | 0.0543475 | 0.155628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779508 | CCAGGGCGCTGCGTC[C/G]GAGGGGGTCTGCGTC | 5336 |
| rs139225692 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860181 | ATTATTATTTTTTTT[A/T]TTTTTTGTAAAGGTG | 5336 |
| rs139234505 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851501 | TTACTCTTTTCACAT[G/T]GCCTTTTTGTTGTTG | 5336 |
| rs139250459 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854037 | AGGTCAAGGTCAACC[A/G]GACAGTTGACCTTTA | 5336 |
| rs139252338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948222 | AAATTGTTCTCTGCA[A/G]GTAAATAGTTTCTCC | 5336 |
| rs139280368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818068 | TCACTTCCTCTCTGT[C/T]GGCTCGTGTCCCCTG | 5336 |
| rs139297646 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821462 | GGCTGTTGCCTTCCT[C/T]GAGGGCTCGAATGCT | 5336 |
| rs139307832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826887 | AGTTCTTCTTCTGTA[C/T]CCATTTGAGGTCTTG | 5336 |
| rs139313863 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795115 | AATGTGCTTGTCACT[G/T]GGGATAAAGTAGTGA | 5336 |
| rs139325562 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925715 | CAACCTGGTAAAACC[C/G]TGTCTCTACTAAAAA | 5336 |
| rs139333012 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863905 | GAGTCCATTTATCTC[A/T]TTCAGCGTGAATGCA | 5336 |
| rs139337893 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799518 | TAGCCTTGAACTCCT[A/G]GCCTCAAGAGATCCT | 5336 |
| rs139377884 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948698 | CCTGGGGAGACCTGG[A/C]GGGACACAAAGGCCC | 5336 |
| rs139381037 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926488 | TGTTGTTAGTGTTGT[A/T]ATAAAGATAGGGAAC | 5336 |
| rs139398781 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859002 | TTAGAAAGTTGGAAG[A/G]CTCCTCCTTTTGGTT | 5336 |
| rs139422638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800795 | ACTCTATACGGCAAA[A/T]TGCTCCTTGCAGATT | 5336 |
| rs139424957 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922792 | CTAACATTTGCTTGC[C/T]GTGTGGGTGTTCATT | 5336 |
| rs139449579 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815800 | ACACAGTGGCTCACG[A/C]CTGTAATCCCAGCAC | 5336 |
| rs139462941 | snp | A/G | 0.00099221 | 0.0222513 | missense | PLCG2 | GRCh38.p7 | 16:81934526 | GCAAAACCAAGGACA[A/G]CTTAGGTAACATCTT | 5336 |
| rs139478069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781230 | ATAAAAAGGGAATTG[C/T]ATTATACTCATACAG | 5336 |
| rs139485898 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820566 | ACTCCCCCATTCTCC[C/T]CATGGGAGATCTTGG | 5336 |
| rs139488059 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786303 | TGTGTTCTTTTATTC[A/G]TCTTAAAATGAAAGC | 5336 |
| rs139504585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876606 | TTAGCTACCAGAAGA[A/T]ATTAGTTTATCTATT | 5336 |
| rs139530370 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920267 | TGTGGTTACTTTGTC[-/T]CCATTCCTACCACAT | 5336 |
| rs139538057 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929284 | CCTTGTTCTGGGCAG[C/T]CCATGACCCTCCCTG | 5336 |
| rs139551854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853569 | TGGATCCCTCGCATG[C/T]GTAGTTCACCGTAGG | 5336 |
| rs139565830 | snp | C/G | 0.00127566 | 0.0252231 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907780 | AGTGCCCCAGGTAGG[C/G]GGACACCCTAGCCAC | 5336 |
| rs139566096 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951512 | CTTCATTTAAATAAC[A/G]TAATTCCAATTTCAC | 5336 |
| rs139603366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846677 | GGATAGGAAGACTCA[A/G]TATTTTCAAGATATC | 5336 |
| rs139610832 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808389 | AGAGAGAGGGAGGAG[A/G]GTCCTGAGAGACTGT | 5336 |
| rs139622121 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913020 | TGAGGCACAGCAAGA[G/T]TAAGTAACTTGCTGA | 5336 |
| rs139627018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797714 | GTTGAGATAGGGCAC[C/T]TCTGTGACAACTTCC | 5336 |
| rs139629803 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806687 | TAGAATGCTGAAAGG[C/G]GGATCATGAGGGTCC | 5336 |
| rs139649028 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907095 | ATGTATACATATGTA[A/T]GAAACCTGCACAGTG | 5336 |
| rs139649867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869625 | TAGTGAAATGAATGC[A/G]TGTATGTCTTTTGGA | 5336 |
| rs139686191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910888 | CAAATTCCTGGCACC[A/C]TGACCTGTGTCCTTT | 5336 |
| rs139688458 | snp | A/C/G/T | 0.00429189 | 0.0461614 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927053 | TGCCACCTGGTGACA[A/C/G/T]CGCCCCCATGTCCTC | 5336 |
| rs139720470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789548 | CCCACCTTGGTCTCC[A/G]AAAGTGCTGGGATTA | 5336 |
| rs139734873 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894272 | ATCATTACGAAAAGT[-/A]AAAAAAATTAGCTGT | 5336 |
| rs139751775 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853265 | GAACCTGGGAGGCAG[A/G]CGTTGCAGTGAGCTG | 5336 |
| rs139751819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827070 | GCCCCATGATTGTGC[C/T]GTGGCCTAGGGCTGC | 5336 |
| rs139764162 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795223 | ATGTTGGATCGTGAT[A/G]GACGCTAGGAAGGAA | 5336 |
| rs139768152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792717 | GTAAAACTATCAGCC[C/G]TCATGAGAATTTACT | 5336 |
| rs139774559 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792805 | GGGTCCCTCCTATGA[C/T]ACATGAGGATTATGG | 5336 |
| rs139777058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937276 | GAGAGGTGAAAACTG[A/T]TACATCGTCGTCCAT | 5336 |
| rs139782584 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849639 | TTCCAGGTCTGGTGG[C/T]GGATGCCTGTAATCC | 5336 |
| rs139782896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810785 | GCAAAGCACTGTATT[C/G]AGTTCTGATAGAAGG | 5336 |
| rs139790675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856223 | TGAGAGCAGCAGTCT[C/T]TGCCATGGGTGTACG | 5336 |
| rs139791862 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894350 | GGGAGGATCGCTTGA[A/G]CCCAGGAGGTTGAGG | 5336 |
| rs139806528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902715 | TCACCTTCTGTGTTA[C/T]CCATTCTCACACTGC | 5336 |
| rs139812084 | in-del | -/GGA | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936938 | TTAATAAGTCCCCGT[-/GGA]GGAGGCACATGTAGG | 5336 |
| rs139812594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851632 | ATTCTTCTGCCTCAT[C/T]CTCCCAAGTAGCTGG | 5336 |
| rs139814662 | snp | C/T | 0.00259529 | 0.0359292 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889123 | TGGGAAATGAAGAAT[C/T]TTATCAGTTCTCACT | 5336 |
| rs139817920 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865303 | TTCCTCCCCTGCAGC[A/G]ATGGGGGCTCAGCCT | 5336 |
| rs139825416 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920156 | ATAAGGATGAGGGTT[C/G]ACAGGTGACTTATCA | 5336 |
| rs139857058 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834564 | AGAGAGCACTCGTCA[C/T]GTGGTTGATAGACCC | 5336 |
| rs139869432 | snp | A/G/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799738 | GCTGGGACTACAGGC[A/G/T]CCCGCCACCACACTT | 5336 |
| rs139889652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857868 | ATGTGTTAAATGGGA[A/G]TATAATAGTACTTCC | 5336 |
| rs139890311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831585 | GGACCCCTGGCTGGG[C/T]CTCTGACCAGTGCTG | 5336 |
| rs139890570 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896798 | GTACAGGTGATCATA[C/T]TGATTCTTTGCCACA | 5336 |
| rs139935992 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777971 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 5336 |
| rs139938294 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789309 | TCGCTCTCTGTTTTA[C/G]AGACAGGGTCTTGCT | 5336 |
| rs139966263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878372 | TGATTGCACCTTGCA[A/G]AGACCCTAATTCCAA | 5336 |
| rs139975981 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815359 | ACAGTGAGATCCTTC[G/T]GTGTAGCTGAGCCTC | 5336 |
| rs139983000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780755 | TTCTTGGTCAGGCAC[A/G]GTGGCTCACACCTGT | 5336 |
| rs139989281 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927399 | TAATCAGGTTGTGTT[C/G]GGCTTGGAAGGATTT | 5336 |
| rs139998242 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883778 | CCCCTGGGAGATAAA[C/G]TAGCACAGCTTTCCT | 5336 |
| rs140025721 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943104 | CTATTGGAGTGTAGG[C/G]GCTACCTGATAGCCT | 5336 |
| rs140027301 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951256 | CGTGTCAGCCACTGT[A/G]TCCAGCCCTCAAAAG | 5336 |
| rs140033248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878580 | TCCAAGAGCTGTCTA[C/T]GCTTCCCTTCTTCCT | 5336 |
| rs140035456 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900490 | AGGGCAGATGTGGGG[G/T]TTGTGCCCCCCGAGC | 5336 |
| rs140039435 | in-del | -/T | 0.0973687 | 0.197999 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916138 | CTTTTCTTTCCTCTG[-/T]TTTTTTTAGAAGGAA | 5336 |
| rs140042892 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902419 | CAAGTTGTAGGCTGC[C/T]GACTTCTAGTTGTGT | 5336 |
| rs140068325 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949631 | AGTCAGAAAAGAAAA[C/G]TTTTAGATAGGGAGG | 5336 |
| rs140070662 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946338 | ACGGCCCGTGAATAC[A/C]ATTGGCAGATGGACT | 5336 |
| rs140080521 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824004 | TCTGTTTCTTTTTCT[C/T]TTTCCTTTCCTTTCC | 5336 |
| rs140083359 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943357 | ACATATTTACATGGC[C/T]AGCAGGAGGAAAAGA | 5336 |
| rs140086442 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889561 | GCTTAACTCACTTAG[A/C]GCCAGCTGAATGGGA | 5336 |
| rs140103404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886368 | GGTCACACAGATGCT[C/T]ATATGGAATAATCAC | 5336 |
| rs140108285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900935 | TACTAACACTGTGAC[C/T]TTAGGCAAAGTCATT | 5336 |
| rs140145309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806314 | GGCAGGTACTATGAT[A/C]ATCATAGTGGTGCTC | 5336 |
| rs140146128 | in-del | -/CCAACTCC | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940484 | AACAATCTCGAGGGT[-/CCAACTCC]CCAAACCCTTCAGAA | 5336 |
| rs140159850 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926242 | AGACTGTGCTGGGCC[A/G]TGGCTGCCATGTTGA | 5336 |
| rs140181910 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843817 | ATGCTGGGATGAAAG[A/G/T]AGAACTCAATAGAAT | 5336 |
| rs140182620 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808878 | GGGGCTTATCAGAGC[A/G]TGCTGGAGGGGCTCC | 5336 |
| rs140189909 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783545 | GGGGCTTGGGACTCA[A/G]GTGAGGGTTTTGATC | 5336 |
| rs140190236 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807611 | ACAACTGTATGTGTT[C/T]AATACGCATTATTTC | 5336 |
| rs140199639 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917411 | CTTCAGATATATACC[A/G]AGAAGTGGGATTGCT | 5336 |
| rs140211608 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778206 | CATAGTGAGACCTCA[C/T]GTCGAAAAAAGAGAA | 5336 |
| rs140213432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852093 | CTGAGATCTCCTTTC[C/T]CACTCTCATCTCCAG | 5336 |
| rs140215528 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812508 | GAAGTGTCTGTTCAT[A/G]TCCTTTGTCCACTTT | 5336 |
| rs140222726 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882783 | TGGCTCACCCCACCT[A/C/T]GTTCTGGCTCATCCC | 5336 |
| rs140233812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879779 | TGTACAATGCACAGA[A/T]AATGGGCTGGTGCAA | 5336 |
| rs140247098 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827573 | GCAGCTGGATAGGTG[A/G]CCTAAATAAGAGAAG | 5336 |
| rs140276699 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954783 | TTTGCTGTTGTACAT[A/G]GTGCTGCAGTAAACT | 5336 |
| rs140284969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797923 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTA | 5336 |
| rs140291541 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795887 | ACCTTCTATTGAACA[G/T]AATTTGGCATGTGAC | 5336 |
| rs140324192 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804472 | ATGTTAGCTTGCAGC[A/C]CATGGGCATGGACAC | 5336 |
| rs140331036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946966 | ATCTGGGATTTGTGC[A/G]TCTATTGCCCGGGGA | 5336 |
| rs140335244 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903326 | GTAGGGAGACAAACC[C/T]GTCAACAGAGAAACA | 5336 |
| rs140341432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901708 | GTCATGAGTGTTTTC[A/G]TATCCCGTTTACAGT | 5336 |
| rs140358179 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919426 | CAGTAGGGTTTGTGT[-/A]AAAATTGTTTGGCCA | 5336 |
| rs140363214 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944935 | TTGTAATTTTTTTTA[C/G]TGTTGCTGTATGTTT | 5336 |
| rs140364937 | snp | C/G | 0.108048 | 0.20579 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957247 | GAGGTTGCAGTGAGC[C/G]GAGATCACACCATTG | 5336 |
| rs140365947 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923911 | CCATGCATTGTCTAA[C/T]CAAATCTTCAACCAA | 5336 |
| rs140383644 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844483 | CATGCCCCCATGCCC[A/G]GCTAATTTTTGTATT | 5336 |
| rs140420405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782802 | TTGAGTGGTAAGGGC[C/T]CCTCCAACAGTTGAA | 5336 |
| rs140446395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842368 | CATATGCCGGCCTGG[A/G]CAGGGCCTGTCCTCC | 5336 |
| rs140446834 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921622 | ACTGACCTCCTTGCA[C/G]TGCAAATGCTATCTC | 5336 |
| rs140454408 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878969 | AACAAGCAGAGTGTC[C/T]GGGCAGGGAGTTGCA | 5336 |
| rs140455097 | snp | A/C/T | 0.0135201 | 0.0812654 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891390 | AGCTGTTCTTCCCCC[A/C/T]TGGTGGGCGCAGACC | 5336 |
| rs140465427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841999 | CACCTTGGTGGAGCC[C/G]TCCTGGGGCCACGTG | 5336 |
| rs140466131 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870060 | CCTGGAAAAATTATC[C/T]CATTTTATTGCTTAT | 5336 |
| rs140482100 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805336 | AACTCTGTCTCTACT[A/G]AAAATATAAAAAATT | 5336 |
| rs140509793 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931231 | TTAACCTAAGTACAT[C/G]TGCAACGACCCTATA | 5336 |
| rs140525315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854990 | TGAGGCGGGCAGATC[A/G]CTTGAGGTCAGGAGT | 5336 |
| rs140532745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903087 | CCAAAGCTACCATCT[C/G]CAAATACCATTACAT | 5336 |
| rs140532877 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866367 | TGCTCCCAGGTTGAG[C/T]TCCACTGGGGCACCA | 5336 |
| rs140532919 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839890 | ACCTTGTCTCTACTA[A/C]AAAGAGAAAACTTAG | 5336 |
| rs140543304 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953069 | CTGCATCGCCTCAAA[C/T]AAATTATAAGAAGAC | 5336 |
| rs140545777 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892723 | GTCAACTTGTGTCAT[A/G]GAGGTTTGCTGTGCA | 5336 |
| rs140547757 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909205 | TGGGCAATGAAAAAG[C/T]AGTCACTCAAATGAT | 5336 |
| rs140552921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918198 | GTAGAAGCCTCTTAG[C/T]TTGATAAAATCCCAT | 5336 |
| rs140555758 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960368 | GACTAGTAACAGGCA[C/T]ATTCTGAAAGATGGA | 5336 |
| rs140592379 | in-del | -/CAAACAAACAAA | 0.115088 | 0.210473 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957296 | AGAGGGAGACTCTGT[-/CAAACAAACAAA]CAAACAAACAAACAA | 5336 |
| rs140604145 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830515 | TTTCACCACGTTGGC[C/T]ATGCTGGTCTTGGAA | 5336 |
| rs140604250 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810895 | GACTATATTTATAAC[A/G]AAAATGAAGGTAACT | 5336 |
| rs140604704 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798555 | CATCACAGCCTGGGG[A/G]CCACTCCACTGTCAC | 5336 |
| rs140608512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787568 | AATAGATTGATTGAG[A/G]CATAATTCACATAGT | 5336 |
| rs140615628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785258 | TGGCCGTCACCCCAG[C/G]TGCTTTGCTGGGGCA | 5336 |
| rs140643132 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829553 | CCATGATACCTTTGC[C/G]AAAAGTGAGAAATTA | 5336 |
| rs140655514 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872709 | GAAAGGTGTGAGGGC[C/G/T]TGGGGAGTACCTGGA | 5336 |
| rs140662156 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934962 | TATCTCCTATCGGGT[C/T]CCTCCCATAACACGT | 5336 |
| rs140662374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872205 | TGGTGGTGTGCACCC[A/G]TAATCCCAGCTACTT | 5336 |
| rs140681224 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828496 | ACCCATCTCGGCCTC[C/T]CAAAGTGGTGGGATT | 5336 |
| rs140696241 | in-del | -/AACACACACAC | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778069 | ACAAAAAAAACCAAA[-/AACACACACAC]ACAAAAAAAACGCTA | 5336 |
| rs140709361 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943779 | AATCACATTGTAGCG[A/T]TAGGGAAAAATAGGT | 5336 |
| rs140760111 | in-del | -/CAAAAAAAAAAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849771 | AGCAAAACTCTGTCT[-/CAAAAAAAAAAAA]AAAAAAAAAAAAAAC | 5336 |
| rs140760413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903745 | GTGCTCTTCCCTGTT[C/G]CCAGCTCATTCCTTC | 5336 |
| rs140763460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947272 | GTAGGGAGCCAGGGG[C/T]GTTGTGTGGGGTTCT | 5336 |
| rs140765953 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829360 | GTGATCTGCCCGCCT[A/C/T]GGCCTCCCAAAGTGC | 5336 |
| rs140771689 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793619 | TGAGTGACGGATTCT[C/G]AAACATATGAGCTGT | 5336 |
| rs140779455 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811177 | TGGGCTTGCCTCCTG[A/T]GTCTCCCATTCTGTC | 5336 |
| rs140797952 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850670 | ATTTTAAAGGGGCTA[A/C]AGTAGGCAGGGAGTG | 5336 |
| rs140824683 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892557 | GAAATTGATTTCACA[A/G]TTCTCTCTTCCCCAC | 5336 |
| rs140825090 | in-del | -/CC | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948406 | GCACATTTGAGAAAA[-/CC]CTGGCTGCCCCACGA | 5336 |
| rs140833314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881313 | TTCCTTGTTAAACAG[A/G]TTTAACTGAATTAAA | 5336 |
| rs140852962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946509 | GTAGGAAAGGGTGCC[A/G]GTACTTGTAAGTTCC | 5336 |
| rs140864062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944628 | CATCACTGTGCCCAG[C/T]TAAATTTTTTATTTT | 5336 |
| rs140875009 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824041 | TTCCTTTCCTTTCCT[G/T]TCCTTTCCTGTCCTG | 5336 |
| rs140877512 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925438 | TTGCCAGAAGTGGGT[C/G]TGGAGAAATGGTGCG | 5336 |
| rs140877714 | snp | C/T | 0.00159981 | 0.0282373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859203 | GATCACTTTGGATTT[C/T]GATCCTCATTCTATC | 5336 |
| rs140879259 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791402 | ATAAACAAGCAGATT[A/T]GTGGGTCATAGATCT | 5336 |
| rs140908912 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848158 | AGAACAGGATCAAGA[A/G]CGCAGAAATAGACCC | 5336 |
| rs140921325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788315 | AGACAGAGTCTCGCT[C/T]TGTTGCCCAGGCTGG | 5336 |
| rs140941252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923073 | AGGCTTGCTGAGCAC[C/T]GGCACTGTGATGACA | 5336 |
| rs140943078 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947972 | CCCTTTTCTACTTCA[C/T]AGACGACTTTAAATG | 5336 |
| rs140943185 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880110 | GCCGGGCATGGTGGC[A/G]CATGCCTGTAGTCCT | 5336 |
| rs140976184 | snp | A/C | 0.0182019 | 0.0936463 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962705 | GCAATCTGCCCAGAA[A/C]TTTTTTTAAAAACTG | 5336 |
| rs141003838 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926149 | TAGGCAGCATGGCAG[A/G]GGCATGATAGGGACG | 5336 |
| rs141005933 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899188 | GTGAAACTCCATTTC[C/T]AAAAGAAAAATAAAT | 5336 |
| rs141008652 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810644 | TTCTGCAATTTCTTT[-/C]TTTTTATTTTTTGCT | 5336 |
| rs141013922 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803142 | TTTTTTTTGTGAGAC[A/G/T]GAATCTCACTCTGTC | 5336 |
| rs141020929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832431 | ATCTCACTCTATCAC[C/T]CAGGTGGGAGCGCAG | 5336 |
| rs141021204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924344 | CTGGACCTGGCTTAG[A/G]AATCTGAATAGCAGC | 5336 |
| rs141027112 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953683 | CTTGACTAGAGTGGT[-/G]GTTCCTCAAGTCAAG | 5336 |
| rs141049260 | snp | C/G | 0.000819926 | 0.0202309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937923 | AGCCAGCCCTCCCTT[C/G]CTGCCAGGGGAGCCA | 5336 |
| rs141054654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895299 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 5336 |
| rs141057774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784100 | GATTAGTCTGTTTCC[C/G]CATGGGCAGAGAGCA | 5336 |
| rs141077980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868808 | TCCTCCATGACCATT[C/T]CTGAAGGGTGGAGAC | 5336 |
| rs141121447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812929 | CCATTTATTAAGTAG[C/G]GAATCCTTTCCCCGT | 5336 |
| rs141123814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906487 | TGGAGTGTGGTGGTA[C/T]GATCTTAGCTCACCA | 5336 |
| rs141124014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931305 | AGGACCCTACTGAAT[C/T]TACTGCATCCCTTGA | 5336 |
| rs141137598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929975 | GTTTGAACTGAGCCT[C/G]AGTTTTACTACTACT | 5336 |
| rs141146998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863118 | GAAGTATATCATGTT[G/T]TCATGCTCCCGTCAC | 5336 |
| rs141149204 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901628 | AACCTGTACATAAAA[C/G]TTAATACTTCCTTCC | 5336 |
| rs141151445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879686 | CTAAGTGCTTATCCA[A/G]TCGCAGTGTCATTGA | 5336 |
| rs141161130 | in-del | -/T | 0.148996 | 0.228688 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806129 | AAAATCCAGTGTGTG[-/T]TTTATACCTATAACA | 5336 |
| rs141185023 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822067 | CCTTACGCTGCAGAG[A/T]TGCTGCAAATAGGGA | 5336 |
| rs141192488 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822508 | ATGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 5336 |
| rs141239808 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803878 | ATACAGACAGGGTTT[C/G]ACTATGTTGGCCAAG | 5336 |
| rs141242816 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882470 | TCGTGGCTTCTGAGG[A/G]GGCCCTTGGGTCTGG | 5336 |
| rs141257242 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855756 | GGTTTTGAGGCTTCA[C/G]TAGGAGTTTGGAGGA | 5336 |
| rs141266744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863448 | GCTTATCTACTTCTC[C/T]ATCGATGGACACTTG | 5336 |
| rs141273259 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845441 | ATCACTATCACTCCT[G/T]TTGTTCACATGAAGA | 5336 |
| rs141286650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919817 | ACAACAAAGACCCTG[A/C]CGTTGTGCTGCTTAT | 5336 |
| rs141294329 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805235 | CCAGGCTCGGTAGCT[C/T]ATGCCTGTAATCCCA | 5336 |
| rs141294634 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961501 | ATTATAGGATACTAT[A/T]TAATACTTTTGGTAC | 5336 |
| rs141302098 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81791550 | GATGGCTGGAAGACT[G/T]AGCTTAGCTGGGATT | 5336 |
| rs141336756 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958515 | CAGCCTGCTCAGTTC[A/G]ATGTACTTTAACTAC | 5336 |
| rs141349608 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914650 | GGGCTCCAGAGATGC[A/G]GGAGTGATAAAAACA | 5336 |
| rs141354037 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848372 | GGGCTGGCTTCCAAA[G/T]GGTGCTTGTTTGGGC | 5336 |
| rs141369813 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955002 | CCTCGCCAGCATCTA[C/T]TGTTTCCTGACTTTT | 5336 |
| rs141383842 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799317 | CTTTATTCACAAGAC[A/G]TTTTCACAACATGCG | 5336 |
| rs141403225 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912484 | GATTTCCATGGTCGT[A/T]TCCAGGGCCAGGTTC | 5336 |
| rs141404588 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827910 | AACCTGATCAACATG[G/T]AGAAACCCCGTCTCT | 5336 |
| rs141406568 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854692 | TGCTCACTGATGTGT[A/G]TTTGGGGTCATGGTT | 5336 |
| rs141407473 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939286 | GACCCAGAGGATCAG[C/T]CTAACCTGGGAGATC | 5336 |
| rs141412980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796187 | CTAGAGCTGCTGATG[G/T]TGATGTCTCTTAGAC | 5336 |
| rs141414476 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873502 | ATCTTATGCAATTGA[C/G]CAGGATTGAGAAAAG | 5336 |
| rs141438413 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935745 | ACCCACATTGCAACC[C/G]TACCTGTGGGCTTTG | 5336 |
| rs141447790 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793238 | CATAGAGTTAAGGAG[C/G]TGGTTGTCTGTGAAT | 5336 |
| rs141452730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904535 | CTGCAGTGCTGTTTG[C/T]ACCCCGGTCGCCTTA | 5336 |
| rs141455533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794949 | TTCTTGATGGTGCTA[C/T]AGCCCTTCTCTTATG | 5336 |
| rs141465231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890106 | TAGAGCCATGCGAAC[A/G]CCCGAAAAGACGTCT | 5336 |
| rs141471585 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852323 | AGTCACTGAGCCAGG[A/G]CACTTGGGTCATTCC | 5336 |
| rs141480003 | in-del | -/GATT | 0.103794 | 0.20279 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859505 | TTGTGACAGGAGAGA[-/GATT]GATTGACCGTGAAGA | 5336 |
| rs141488015 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825036 | TGGCCTCTAGAGCTG[A/G]GAAAGGCAATGGGTG | 5336 |
| rs141488164 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851426 | TACGAAATCTTGTCA[C/G/T]GTGTAGGTGGGTATG | 5336 |
| rs141494299 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800531 | TCATCTATGTCCCTG[C/T]GAAGGACACGATCTC | 5336 |
| rs141495169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794053 | GCAGGACAGAAACAC[A/G]TGAATTCCTTACGTG | 5336 |
| rs141507346 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896940 | CTTTTCTGTCCCACC[A/G]GAAGATCTTGGTCTG | 5336 |
| rs141513236 | snp | C/T | 0.000483434 | 0.0155397 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939856 | AGAAGGGGGCAGCTC[C/T]AATGTGGCCTCTCAT | 5336 |
| rs141531769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895533 | CCACTGCACTCCAGC[A/C]TGGGCAACAGAGCGA | 5336 |
| rs141549335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945722 | TATGAACTACTAAGG[A/G]ACAGAAAGATTTCCT | 5336 |
| rs141564515 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792295 | GAGACCAGCCTAGCC[A/T]ACATGGCGAAGCCCC | 5336 |
| rs141587683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942573 | TAAACCAGTTGGAGC[A/G]CAGGAAGGAAAGCAG | 5336 |
| rs141593245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885459 | GTGAGGCACTGTGCC[C/T]GGCCCACTTTGCCAG | 5336 |
| rs141594055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849112 | TGGGGTTGGAGGGGT[C/T]ATCACAGGGCTGTGG | 5336 |
| rs141597852 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900013 | CCAATAGATAAGAAA[A/G]ATCAACTACAGATAC | 5336 |
| rs141610541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789089 | CTGTGTAACAAACCT[G/T]CATGCTCTTCACATG | 5336 |
| rs141615226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941533 | GTTACTAGATGAAAC[A/T]AGACTTTGGGAAAAT | 5336 |
| rs141629566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835770 | TCAAGGTGTTGGTAG[G/T]GCAGTGCTCCCGCTG | 5336 |
| rs141633110 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900320 | AAAAAAGATTAGAGA[C/G]TTTTTTCTGTAAGTT | 5336 |
| rs141636099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846027 | GTTCTTGTGAGGAAC[A/G]ATGAGTTAATACAGA | 5336 |
| rs141685932 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875525 | AGTAGAGAGAATAGC[A/G]TAACAGACCCCCATG | 5336 |
| rs141685990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898020 | TAGCCCTTCTAAGTG[C/T]CAACCTCCATCAGGC | 5336 |
| rs141690434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833183 | AGCATGAGGATACCA[C/T]GTTTGGGGTTCAGCA | 5336 |
| rs141693204 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840232 | GCTTAGAATTGAGCC[C/G]TGACAGCTGGCCCCT | 5336 |
| rs141693337 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815433 | GACCCTGTCTTTCCA[C/G]CGGGAAACTGCAGGG | 5336 |
| rs141711666 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834402 | GCGCGGGTGGTGTTG[A/G]AGAACTCTGGGCCTG | 5336 |
| rs141716135 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838255 | CCATGCCTGGCTAAT[C/G]TTTATATTTTTAGTA | 5336 |
| rs141718134 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814212 | GGGTCTGAAGGATAG[A/G]CTGTCTTTTTGCTTG | 5336 |
| rs141718763 | snp | A/C/G | 1.70261e-05 | 0.00291766 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81785949 | CCCTTTCAGCTTCCT[A/C/G]ATTTCTCCCGATTCC | 5336 |
| rs141724460 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779656 | CCCGGGCCGGCGCCA[A/C]CTCTCCGGTCCGTGC | 5336 |
| rs141729703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876127 | AACTCCCTGGCTCAG[A/C]TGATTCTCCCACCTC | 5336 |
| rs141740715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896710 | TTCTACAGGCGGAAT[C/T]CAAGCAGCCAGTAAT | 5336 |
| rs141743621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879188 | GCCACACACTGGGCT[C/T]CCTCCAGATGTAAAT | 5336 |
| rs141747389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842658 | TTGGGGAAAAAGCCA[C/T]GTTCCTGGTGTCAGG | 5336 |
| rs141755615 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939511 | TGTGAGGCTGGGCTC[A/T]CCCCTGCCAGCTGTA | 5336 |
| rs141759444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836889 | TACATGAGTGCACAG[C/G]TGTCAGGACCCCTGC | 5336 |
| rs141764477 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877268 | GACCATCCTGGCTGA[A/C]ACGGTGAAACCCTGT | 5336 |
| rs141767011 | in-del | -/TGCA | 0.313082 | 0.241911 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940202 | GGCTTGGAGAGCAGG[-/TGCA]GTGTACAGCCTGTCG | 5336 |
| rs141827939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932415 | GTCTTCGATGATGGA[G/T]TAAGGGCTGTCTGTT | 5336 |
| rs141832072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928343 | ACGGATTGGAAAATG[A/T]AACTCCGAACCTCCT | 5336 |
| rs141860914 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958985 | TTCAAATGCAGCCAT[C/T]TCCCTTGGGGCAGAT | 5336 |
| rs141868099 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926568 | GTGTACTAGGTAGGC[A/G]CTGTCCCAAGCACTC | 5336 |
| rs141869694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781560 | TTTAGTAGCTGCTCA[C/G]AGGTTGCCCTAAAGG | 5336 |
| rs141891101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816791 | ACAGGCATTAGCCAC[A/G]GTGCCCAGCCAGAAA | 5336 |
| rs141892788 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780164 | GGGGCGGGGTGGTAA[A/C]GGGGTGACATGGCGC | 5336 |
| rs141935868 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886385 | TATGGAATAATCACT[G/T]CAGCACTTTGTGTGC | 5336 |
| rs141941061 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927888 | ATGTGGTTGTGTTCC[A/G]TGTGCTTGGGCTGAG | 5336 |
| rs141950806 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884933 | CACCCCCTTGCCCAG[G/T]CTGGAGAGCAGTGGC | 5336 |
| rs141955636 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810191 | AGATGGGGTTTCACC[A/G]TCTTGGCCAGGATGG | 5336 |
| rs141984757 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924879 | TGTCCGTCTGCTTCT[C/T]CCAGTTCAGAGGCTC | 5336 |
| rs141992122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954072 | GTCTTGCCCAGGCTG[A/G]AGTACAGTGGCATGA | 5336 |
| rs141996694 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807467 | CAGGAAGCCCATCAA[A/G]CCCCCACATCGTCAT | 5336 |
| rs142001658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952396 | GGATTCTCAATTCCA[G/T]ATATTGCTAAATATC | 5336 |
| rs142006523 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888886 | TTGCCTACGGATCAT[C/T]TGTGGCTGCTTTTGC | 5336 |
| rs142010836 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930788 | ATTATTTATTCTTTA[C/T]ATGTAAAAGATTATA | 5336 |
| rs142022471 | snp | C/G | 8.28109e-05 | 0.00643418 | missense | PLCG2 | GRCh38.p7 | 16:81869219 | TCTTTTGCAGCATCA[C/G]TCTCCGAGAGTTGAA | 5336 |
| rs142030124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929809 | AAGGTCCTAAGTGAC[C/T]GACCACCACATGTGC | 5336 |
| rs142036806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817026 | GCACTGGATGCGTTA[C/G]ATGCTGGGGAAATAG | 5336 |
| rs142052005 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914258 | TGACACAACCGGATC[A/G]GGGCCTCACCTGATG | 5336 |
| rs142075604 | in-del | -/GGT/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955620 | CTCACTCAGTGGCTG[-/GGT/GT]TTTTCCTCTTTTTCT | 5336 |
| rs142092577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887654 | TATTTTTCATTGTTT[C/T]GGACATTGCATCCAG | 5336 |
| rs142098187 | snp | C/T | 2.88538e-05 | 0.00379817 | missense | PLCG2 | GRCh38.p7 | 16:81889263 | CTGAGCCTTTCTTGT[C/T]TGTGGATGAGGTGAG | 5336 |
| rs142099020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851809 | TGGGCCACCAGTGCC[C/G]GGCTTGTTTTCACAT | 5336 |
| rs142100765 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866887 | CAGCTGTTCCTTGGA[C/G]CACTCCCAGGGCTGA | 5336 |
| rs142103409 | snp | A/C/G/T | 0.00199529 | 0.0315338 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807890 | ACAGCCAGATCTCTC[A/C/G/T]AGAACTCACTGAATA | 5336 |
| rs142108360 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949448 | TCCTCTTTGGTGCTG[A/C]AAACTAAAAGACTCC | 5336 |
| rs142126670 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957353 | CCTTGACTCTAGTTC[C/T]CTTTGTTCTAGAAAT | 5336 |
| rs142131380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827295 | AGGATCAAGTGATCT[C/T]ATCTCAGTCTCCCAA | 5336 |
| rs142131420 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807200 | CACAGGGTCAGCTCC[A/C]CATGTCTTGTCCCAG | 5336 |
| rs142140333 | snp | A/G | 0.00182875 | 0.0301833 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81870887 | TGAGCTCAGCTTTGA[A/G]CAGTTCCATCTCTTC | 5336 |
| rs142152450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869451 | GACAGAGGGATCATG[A/G]ACATATCTGAGGACC | 5336 |
| rs142167125 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826622 | TACTCAGTGCTTCAA[A/C]TGGTGATAGCAGCAG | 5336 |
| rs142172570 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827329 | CCTGGGACCACAGGT[C/G]TATGCTCCCATGCGC | 5336 |
| rs142174816 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795630 | AGAGGAAGAGCAGAG[C/G]ATGGCTCAGGAGGTT | 5336 |
| rs142191653 | in-del | -/TTGA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859511 | CAGGAGAGAGATTGA[-/TTGA]CCGTGAAGAAGTAAA | 5336 |
| rs142192435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868520 | TTGGTTCCTCTGGGT[A/G]GCAGGTAGAGTCAGT | 5336 |
| rs142200863 | in-del | -/AAATC | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948166 | TAGCAATGGAATAAT[-/AAATC]AAAGAAAAAAGGACC | 5336 |
| rs142205534 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886867 | TATTTTTATTTTCAT[A/C]CTTATTCTTTGCCAT | 5336 |
| rs142208528 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846615 | AGCAGAACATCGGGC[-/T]TATGGCTAATGCTTA | 5336 |
| rs142216358 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946763 | CTTTTTCCTCCTTTA[C/T]GCCAGAATTCTTTCC | 5336 |
| rs142223658 | in-del | -/GTT | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787932 | GCAGAATCACGATAC[-/GTT]GTATGGGTATTCCAC | 5336 |
| rs142227086 | snp | A/C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961196 | GAATTCAGTGATTCT[A/C/G]CTATCATAAAGCTTC | 5336 |
| rs142249173 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791033 | TAAAATAGGGTTTTG[C/G]TCTGAACCCTGTTTG | 5336 |
| rs142275175 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808595 | GCCTCCCAGATTCAA[A/G]CCATTCTCCTGTCTC | 5336 |
| rs142277407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847477 | ATCACATCGTTGGTT[C/T]CCCTGGCAGCCAACC | 5336 |
| rs142279533 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808580 | CTCGCTACAACCTCC[A/G]CCTCCCAGATTCAAG | 5336 |
| rs142287797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809705 | AGCCTGTGTGTGCCT[A/G]TGCATGTGTCTTTCT | 5336 |
| rs142287870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944460 | ATATGCAAATACTAC[A/G]CCACTGAATTAATTA | 5336 |
| rs142298179 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901329 | TGCCTAGGGATGCCA[C/T]GGTAACATTTGGATT | 5336 |
| rs142335703 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920097 | GCACCAAGAGGAAGT[C/G]AGCATGGCCGGAATC | 5336 |
| rs142336349 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955043 | TATTCTTAATAGGGA[-/G]GAAAGTCATTACTAA | 5336 |
| rs142340119 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877534 | AATCCAGGTGTTGGC[A/G]GGGCCACACCCCTCG | 5336 |
| rs142340436 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918926 | AAAAAAGTCACTGTT[C/T]TGCTAGTTGAGTCAC | 5336 |
| rs142346178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941995 | CTTTTAGATTAGTCT[A/G]ATAAGGCTTAGGAAT | 5336 |
| rs142401330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821139 | TCAAATGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 5336 |
| rs142418180 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815983 | AAGAGAATTGCTTGA[A/G]CCCGGGAGGTGGAGG | 5336 |
| rs142420181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941225 | TCTGAGCAGCAGGCA[C/T]GCTAGAAAATCCAGG | 5336 |
| rs142426845 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893235 | GTCATTCTTACGGCA[-/G]GTTTTGGTGGATATG | 5336 |
| rs142427712 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922162 | AGAAAGGCAAGGGTA[C/G]TGCTTAGCCTCTGGC | 5336 |
| rs142443536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854832 | TTCATGGGGGTATTG[C/T]GAGGAGTATGTTAAG | 5336 |
| rs142465920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917486 | ACTGTTTTCCATAGT[A/G]GCTATGCTAATTTAC | 5336 |
| rs142470341 | snp | A/C/G | 0.0123225 | 0.0777027 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855464 | GCAGCTGTCAAAGTT[A/C/G]AGCAATATAGGGACA | 5336 |
| rs142470398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878790 | GCCTTTGGGATGCCC[A/G]ACTGTCTTCCTTATC | 5336 |
| rs142502547 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817881 | CTCCCTGTGCTTATG[A/C]ACATGTTCTCACGTT | 5336 |
| rs142502661 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800155 | TGGGTATCATAGTAC[C/G]TGGCAAATATCCCAA | 5336 |
| rs142515900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800822 | GATTGAACAGATCTT[C/G]AGATGGGGAGATGAT | 5336 |
| rs142523781 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959657 | CTGAAGAAAGAACAT[G/T]CCTCTTAGTGGCAGA | 5336 |
| rs142544454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872427 | CACATTTAATGTTGA[C/T]TTTGTGTGTGTGTGC | 5336 |
| rs142557912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856907 | ATGTGAGGATGGAAA[A/C]AAAGGTCAGCAGATG | 5336 |
| rs142570471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934079 | GAACTAGAATTTGAG[A/T]CACTCTAACAGTGTG | 5336 |
| rs142578563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829283 | CCGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 5336 |
| rs142579839 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857545 | GTTCTGGTGAGGGCT[C/G]TCTTCCTGACTTGCA | 5336 |
| rs142585673 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780981 | GCAGTGAACCCAGAT[A/C]ATGCCACTGCACTCC | 5336 |
| rs142608151 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949912 | AGTAAATAAACTATA[C/G]TGCAGAGGGAGATTT | 5336 |
| rs142612993 | in-del | -/A | 0.0715223 | 0.175059 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782302 | TATTCAAACTCAGCC[-/A]TATTTGTATTTACAA | 5336 |
| rs142625805 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811145 | CGTATGACAGCAGTG[C/T]TGGGGTTGAACAAGC | 5336 |
| rs142646723 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907621 | ACGCCCTGCAGGGCT[C/T]CTGGGCTCCACAGTT | 5336 |
| rs142647352 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780621 | GCCTTCCCCCACCAG[A/C]GACTGGAGTATGGGC | 5336 |
| rs142662858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869907 | TGCTTACAGGGAAAT[A/G]CTCATTCTTCTTAGG | 5336 |
| rs142671992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843386 | CTTCTTAGCTGAATC[C/T]AGTACATTCCTGAAA | 5336 |
| rs142673803 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805582 | TAAGAAAACAACCCA[A/G]TTAAAAAGTGGGCGA | 5336 |
| rs142696091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836210 | GCTGACCCAATCCCT[A/G]CATTTCTCAGAGGGG | 5336 |
| rs142704158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903893 | GGCCCACTTCTTTCT[A/G]TTTCAAGAAATGAGG | 5336 |
| rs142706260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840732 | TCCTGCTGTGCGGCT[C/G]GATTCCTAACGGGCC | 5336 |
| rs142707750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867175 | CGTCTCCAGGGCAGC[A/G]GCTGGGCAGTGACGC | 5336 |
| rs142709966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931035 | TTCTTTTGATCAAGA[C/T]GAACACATGTCTATA | 5336 |
| rs142742653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788809 | CATGTGGAGGTGGCC[A/G]TCTTCCCTCTTGACT | 5336 |
| rs142778986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807395 | CTGGATCTGAGATCC[A/G]AGTTGCAAAGGAAGA | 5336 |
| rs142792946 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806705 | ATCATGAGGGTCCAG[A/C/G]TGTGGGGCTGGGGAC | 5336 |
| rs142797744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935954 | AGCCTAAAAGGTGGT[C/G]GGAAAACTAGGCCCC | 5336 |
| rs142823422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953126 | TACAAAATAACTGAC[G/T]AGTATTCTTCCAAAG | 5336 |
| rs142825971 | snp | A/G | 0.00272592 | 0.0368175 | missense | PLCG2 | GRCh38.p7 | 16:81923501 | CTCAGAGAACCGTGA[A/G]AGCTCTGTATGACTA | 5336 |
| rs142833673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909683 | CCTCCTGAAGTGCTA[C/G]GATTACAGCTGTAAG | 5336 |
| rs142833782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883432 | CCTGTGCTCACCTGG[C/T]CACCTGTGCTCACCT | 5336 |
| rs142842781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880343 | AATTTATCAAAGCCA[A/G]TGTGCCTACAATGTG | 5336 |
| rs142859528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874178 | ATTATATTATATATT[A/G]AAATCTAGATATTTG | 5336 |
| rs142863579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912774 | GGCAAGGACAGATGC[A/G]GAGAGACAAGGGGGA | 5336 |
| rs142872580 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950547 | AGAAATATACAACTT[C/T]GTGTCCTACAAATGG | 5336 |
| rs142900383 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804921 | GCACTACAAGCTCAC[A/G]TGTATCCATGTGATC | 5336 |
| rs142914707 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894991 | GTAGCAGTTACTCTA[C/T]AGACTTTCTTCCCGT | 5336 |
| rs142914833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856714 | AATACTGCCCTCCCA[A/C]GATGCCCATGTCCTA | 5336 |
| rs142929093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865077 | CTGGAACAGGCAGCT[A/G]GGGAGTCACAACCAT | 5336 |
| rs142941381 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962109 | AGGACCGGTCTTCGG[G/T]CAAGGGTATACGAGT | 5336 |
| rs142947445 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920980 | GCACGCAGCAGGCCA[A/G]GACAGGGCCTCTCTG | 5336 |
| rs142955968 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888471 | AGCTCAGGCAGTCCA[C/T]CCGCCTCGGCCTACC | 5336 |
| rs142974393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849423 | TCTTTAGTTATGTAT[A/G]ATTTTTCTGTAAGGA | 5336 |
| rs142995039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783747 | CCATGGGGGCACCTT[A/G]TTCATCCCTTTGTCC | 5336 |
| rs143010428 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945309 | AATCAGTAGATATGA[C/T]ATAAATGCTTTCAAG | 5336 |
| rs143014916 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828980 | CCATTCTCTCAAACA[C/T]TGCTAGTCTCAGGAA | 5336 |
| rs143025883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791970 | CATAAATCCGAGGAC[A/G]TCACTTGCACCAACT | 5336 |
| rs143032936 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809498 | TCCCTGTCCACCACC[C/T]CATTCCCCTTGCAGT | 5336 |
| rs143058849 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906339 | CTCTATCCCTTTACC[G/T]AATGTGTATATCCAT | 5336 |
| rs143061456 | in-del | -/CTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816649 | TGCCCAGCTAATTTT[-/CTT]AATTTTTTTTTTTTT | 5336 |
| rs143080576 | in-del | -/C | 0.124837 | 0.216412 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915786 | CTCGGCACCCCAGAG[-/C]CCCCCCTGCCTGCCC | 5336 |
| rs143089796 | snp | C/T | 0.119978 | 0.213528 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813053 | CTATTTTGGTACCAG[C/T]ACCATGCTGTTTTGT | 5336 |
| rs143106118 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826454 | GAGGTCAAAGTGCTC[A/G]ACCTCGTGTGCCTCA | 5336 |
| rs143112127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794606 | TTTGGGCCTCCATTT[C/T]CTTATCTATAAAATG | 5336 |
| rs143131374 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788473 | TTTTAGTAGAGACGG[C/G]GTCTCACTGTGTTAG | 5336 |
| rs143148947 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874822 | GAGGATAAGAAATGT[A/G]ATCTCACGTTTGTGT | 5336 |
| rs143149504 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942471 | ATTCATGGGAGGAAT[C/G]AAATAGAATGAACAG | 5336 |
| rs143154621 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831768 | CTTGCCCCAATCCTG[C/T]CTTGTCTGAAAGGGA | 5336 |
| rs143195637 | snp | C/T | 0.00282913 | 0.0375041 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919523 | TCGCATCAACCGGGA[C/T]GGCCGGCACTTTGTG | 5336 |
| rs143196340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926519 | AATGTTTTAGCTGAA[C/T]AATAATAAGAGCTAA | 5336 |
| rs143214451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937175 | ATAGAGATCGTGGGC[A/G]GGGATGCAAATAGGT | 5336 |
| rs143214549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872845 | GAGTTGTGAAGACAG[G/T]CATTTTTAAGTGATG | 5336 |
| rs143220930 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960993 | TACTGTAGAGCATGT[C/T]CCAAGGTGTAAAAAT | 5336 |
| rs143226295 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878891 | GTCCTGCTCTGCGTC[C/T]CAGGGGCCAATTCCT | 5336 |
| rs143229201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839832 | AAAATGGGAGGATCA[C/T]TTGAGGCCAGGGATT | 5336 |
| rs143248102 | in-del | -/TAG | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905612 | TCTTGTTCCCATTTT[-/TAG]TAGTCAAGTGAGTTT | 5336 |
| rs143269352 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873221 | TGTCCTCTCACTTAG[C/G]CTTTTCTATAAAATG | 5336 |
| rs143291650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935587 | GTTAACTTACCGGGA[C/G]GCCAGTCCCTAGGAA | 5336 |
| rs143296899 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893366 | GAGGACCCAGAGAGC[A/G]GCCATGGGGCCTTGT | 5336 |
| rs143299165 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834764 | CAAGGGCTCCCAGGA[C/T]GAGGACAATCTCCTT | 5336 |
| rs143370371 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823230 | GAGGTCTGGCTTCCC[C/T]GGGGCTTTACCTCGA | 5336 |
| rs143372180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870687 | ATAGCATGACTTTTT[C/G]CTTTCAAAAGCCATG | 5336 |
| rs143372861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908996 | GTCTCCTCCATAAAA[C/T]GAGGACTCTAGGGCT | 5336 |
| rs143393250 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813419 | TTCCTAGGTATTTTA[C/T]TCTCTTAGTAGCAAT | 5336 |
| rs143403265 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828864 | TTTTTCTTTTCTGAA[-/T]GCCGAGGTGGGTGGA | 5336 |
| rs143403868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932030 | CTCCTGACAGAAAAC[A/G]TTCACTGAGCTCACC | 5336 |
| rs143408961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813634 | AATTTGGGCAGAGCT[C/G]AGTCAGTGGATTTGC | 5336 |
| rs143415977 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863692 | CCAAGGCAGTGCACA[A/G]GTTTCTGTTTTCTTC | 5336 |
| rs143426125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926397 | GCATGTCTGGGCACG[A/G]CCTTGCCGGGAGGAA | 5336 |
| rs143426277 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861552 | TCATCCAAAATGCCC[G/T]GCCTGCTCCGCCACG | 5336 |
| rs143433272 | snp | A/C/T | 0.0115206 | 0.075079 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903102 | CCAAATACCATTACA[A/C/T]TGGGGATTAGGTTTC | 5336 |
| rs143441994 | snp | A/C/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807397 | GGATCTGAGATCCAA[A/C/G]TTGCAAAGGAAGAGC | 5336 |
| rs143448182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826152 | AGAGATACCACCATC[C/T]AGCCAGGTCCCCATG | 5336 |
| rs143463560 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924632 | CCTGTCCTCTTGCAA[A/G]ATGCCTTAATCCAGG | 5336 |
| rs143465688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868987 | GCATCACCCTACCCT[A/G]TGAGTCTGCTATGTG | 5336 |
| rs143475811 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927673 | ACTCCACCAAGGATG[A/G]TATCTTTGTAATGAG | 5336 |
| rs143497337 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805486 | CCTGGGTAACAGAGC[A/G]AGACTCCATCTCAGA | 5336 |
| rs143499334 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927511 | CACATTTATATTGGA[C/T]AGCCAGACATTGAGA | 5336 |
| rs143545978 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805477 | GCACTTCAGCCTGGG[G/T]AACAGAGCGAGACTC | 5336 |
| rs143566139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804010 | GTGAATAATACTGCG[A/G]TGGACATTCATGTAC | 5336 |
| rs143569477 | in-del | -/ATA | 0.467234 | 0.12373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835583 | GACTCGGTCTCAAAT[-/ATA]ATAATAATAATAATC | 5336 |
| rs143574106 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903674 | AGCTCGGCCATGGAG[A/G]GTCCATGGCTTCTCA | 5336 |
| rs143575989 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807119 | GCATTTCCTTCTCCA[C/G]GTGGTCAGTGGAGAC | 5336 |
| rs143588885 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824029 | CTTTCCTTTCCTTTC[A/C]TTTCCTTTCCTTTCC | 5336 |
| rs143615613 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896232 | CACTTTCAGAACCCC[C/T]GAAAGAGAGGGAAAG | 5336 |
| rs143618645 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785897 | CCTGTTAACTAAACC[C/G/T]CTTTCAGTACTAAAA | 5336 |
| rs143637627 | snp | C/G/T | 0.000482448 | 0.0155244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927199 | TCCCCCTCTTCGATC[C/G/T]TCTTACAGGAAGAAG | 5336 |
| rs143648148 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859652 | CCATTCTCCTGCCTC[A/C]GCCTCCCAAGTACCT | 5336 |
| rs143650265 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818583 | TTATCTGCTTGGTGG[C/G]GGCTGTGTTTCTGGA | 5336 |
| rs143658063 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957086 | GTTGGATCACCTGAG[A/G]TCAGGAGTTCAAGAC | 5336 |
| rs143694433 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919269 | GTCACTCGGCCATAT[G/T]TCTTCTGAGACACAG | 5336 |
| rs143694497 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891203 | AACAATGTATATATG[G/T]TAAGCATAAACCCTT | 5336 |
| rs143711032 | snp | A/G/T | 0.00795939 | 0.0626292 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958867 | GCTGCTTGAAAGAGG[A/G/T]AGACAAAAGTTAGGT | 5336 |
| rs143720355 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81819058 | GGAAGCTGAGGCTCA[A/G]AGAGGTCCAGTGACT | 5336 |
| rs143726363 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801890 | TTCACTATGTTGGTC[A/G]GGCTGGTCTCGAACT | 5336 |
| rs143731879 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824697 | GGGATCCTCTCGTAG[C/G]TGCCATGTGACCTCT | 5336 |
| rs143734787 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805237 | AGGCTCGGTAGCTCA[C/T]GCCTGTAATCCCAGC | 5336 |
| rs143789176 | snp | G/T | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827982 | GTAATCCCAGCTCTT[G/T]GAGAGGCTGAGGAAG | 5336 |
| rs143791455 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888085 | TCATGAGGTATTGTT[C/G/T]CTGGGCCTCTGTTTC | 5336 |
| rs143794108 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813130 | TGCAGCTTGTTCTTT[C/G]TGCTTAGGGTTGTCT | 5336 |
| rs143801660 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832040 | TTGAGCCTGGGCACT[C/T]GGACACAGTTACCAG | 5336 |
| rs143814314 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930025 | TGTGACTTTCTCTTA[A/T]TGAGCCTCAGTTTTG | 5336 |
| rs143821278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806437 | TGTGACATCTGATTG[C/T]TGGGCCCGAGCATCC | 5336 |
| rs143836889 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799966 | ATACTCAAGAGCAAG[C/G]GATCCAGGGTCTGAC | 5336 |
| rs143840723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851514 | ATGGCCTTTTTGTTG[C/T]TGTTGTTGTTGTTGT | 5336 |
| rs143842377 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915389 | CAAAGGAAGTGTTGA[G/T]TTGTTGCCCGGCTGT | 5336 |
| rs143849787 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803533 | CTTTCTTTCCTTTCT[C/T]TCTTTTCTTTCTTTC | 5336 |
| rs143855309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892561 | TTGATTTCACAGTTC[A/T]CTCTTCCCCACCATG | 5336 |
| rs143859339 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961994 | TGATTCGGCTGATCT[C/G]GCTGGCTAGGTGGGT | 5336 |
| rs143861248 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934801 | GGACTCACAGTTCCA[C/T]GTGGAGGAGGCCTCA | 5336 |
| rs143862574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840656 | ATGAGAATCTAACGC[C/T]GCTGATGATCTGACA | 5336 |
| rs143897174 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902034 | GGTCTCAGGCACATC[C/T]GAGTTCCAGCTCAGA | 5336 |
| rs143905052 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798828 | GGGGCTGGCCTCCCC[A/G]GCCTCAGGACTTCAG | 5336 |
| rs143908658 | in-del | -/A | 0.469049 | 0.120489 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832105 | TCCTTTGATAAATGG[-/A]GGGGGGGAATAGTGA | 5336 |
| rs143929666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817018 | GGTGACGGGCACTGG[A/G]TGCGTTAGATGCTGG | 5336 |
| rs143938007 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796549 | TTGTCCTTACCAATT[G/T]CATATGTCAAGGTCC | 5336 |
| rs143948528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913298 | CCTGCATGTTCTTAC[A/G]GTGGTAACAGTCTGC | 5336 |
| rs143949347 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874729 | CATCGTGAGCTTGCT[A/G]GTTCCTCTTTGTGTC | 5336 |
| rs143959073 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879555 | CCTTTCTAGAACCCT[C/G]ATAGTCCCCATGACG | 5336 |
| rs143976869 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947756 | TTTACTTTGCTAGCA[A/G]TATGTTTGTTTAGTT | 5336 |
| rs143985669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854231 | TCTTCAGACTCCAGG[A/G]GTTTGTGGGGTGGCA | 5336 |
| rs143991744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876921 | ACATATGTACGTGTA[G/T]TGTGGGATGCTAGAG | 5336 |
| rs144039406 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946369 | TAAGCCCATTCAGAA[A/T]TGTCTAGCCCAAGCA | 5336 |
| rs144060202 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856207 | CATCTGTGTGGGAAG[A/T]TGAGAGCAGCAGTCT | 5336 |
| rs144064109 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798012 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTCC | 5336 |
| rs144101582 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855546 | ATGTCTTTTGAGCCT[A/G]TACTCTGTGTTAGGT | 5336 |
| rs144105664 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815325 | GGTCTCAGCCTCAGC[A/C]GGTTGGCAGCCACAC | 5336 |
| rs144116792 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954205 | TTCTTTCATTTTTTA[C/T]AGTAACAGGGTCCCG | 5336 |
| rs144126709 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882474 | GGCTTCTGAGGAGGC[C/T]CTTGGGTCTGGCTCC | 5336 |
| rs144127471 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951293 | TAAACTCTTTGCCTA[C/G]TTAATAAAAGAATAA | 5336 |
| rs144128790 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925950 | AGATGTATAATTATA[C/T]GTTAAGTATAAGATG | 5336 |
| rs144161264 | snp | A/G | 0.00454408 | 0.0474488 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783087 | CCCAGAGTGAGGGCT[A/G]GAAAGAACTGAGGAG | 5336 |
| rs144162712 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948717 | ACACAAAGGCCCTCC[G/T]TATGCCTCATCAGCT | 5336 |
| rs144222732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804528 | CTTGAGTCAAGAATC[A/G]TACATTTTAACCATC | 5336 |
| rs144227079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781446 | GTATTTCTATTGCAA[C/G]TATTGCTTCCGTGAT | 5336 |
| rs144238446 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954808 | TAAACTTACATGTGC[A/G]TGGGTCTTTATAGTA | 5336 |
| rs144240099 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777354 | ATATATATGACTGAA[C/G]TAATATATTATGTAC | 5336 |
| rs144252302 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869882 | GATGGAGACAATGGG[C/T]ACCGATTTTTGCTTA | 5336 |
| rs144255365 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827047 | CCTCATGTTTTGCAG[A/G]TTCCTAAGCCCCATG | 5336 |
| rs144267198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931237 | TAAGTACATCTGCAA[C/T]GACCCTATAAGGTCC | 5336 |
| rs144278950 | in-del | -/A | 0.220246 | 0.248223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892537 | GGTAAAATGTCTTTC[-/A]GGGGGAAATTGATTT | 5336 |
| rs144285277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928715 | GGGAGGTGGCTGACA[C/T]AGGGTCCTGTCTTGA | 5336 |
| rs144311607 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803528 | TTGTTCTTTCTTTCC[-/TT]TCTTTCTTTTCTTTC | 5336 |
| rs144326837 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846826 | AAAGGAAAAATCAAG[A/G]TGTGTTTTTTTTCTC | 5336 |
| rs144330655 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806059 | TATTATTTCAACATG[A/T]ATGCAATATAATTAT | 5336 |
| rs144331328 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787746 | CCCTCATCCCCCCTA[C/T]CAGACGTAAGCAACC | 5336 |
| rs144354153 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867638 | TTCAGCTTTTGTTAC[C/T]ATTGTTACTGCTGCT | 5336 |
| rs144356140 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904292 | TTACTGAGACTCTGA[G/T]GATGACTCAGCCAAG | 5336 |
| rs144362843 | in-del | -/TAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800666 | TTGTGATACTATTGC[-/TAT]TATTATTATTATTAT | 5336 |
| rs144363484 | in-del | -/TTTATTTATTTATTTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841205 | GGCCAAAAAGTAAAC[-/TTTATTTATTTATTTA]TTTATTTATTTATTT | 5336 |
| rs144374360 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787188 | GCTTTTGTTATTATT[C/T]GAAGTGACTATCATT | 5336 |
| rs144401565 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844059 | TCGGCTCACTACAAG[C/T]TCTGCCTCCCGGGTT | 5336 |
| rs144402001 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848160 | AACAGGATCAAGAGC[A/G/T]CAGAAATAGACCCAC | 5336 |
| rs144403916 | in-del | -/TC | 0.499631 | 0.0135733 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871854 | GGCACCATCTGAATG[-/TC]TCTCAATGGAGGAAT | 5336 |
| rs144426501 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789915 | TAGGCGCTAGAGATA[A/C]AGCAGTTATTAAATT | 5336 |
| rs144464939 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940323 | CCTCAACCTGGCACT[A/G]CAGTTTGATTTCATT | 5336 |
| rs144466760 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914492 | GGGTCCTCAGGTTGA[C/T]TGCCTGACTTACATA | 5336 |
| rs144470715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853969 | TCCTCTTCCCCCTTT[A/G]ATTGAGCCACAGAGC | 5336 |
| rs144480508 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802729 | GGCATGCGCCACCAC[A/G]CCCAGCTGATTTTGT | 5336 |
| rs144485784 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850160 | TCTACTGTAAAAAGA[A/T]TTGGAGAAAACTGGG | 5336 |
| rs144506954 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861121 | ATGCCAGGGATTGCA[C/T]TGAGCTCTTCAGTCC | 5336 |
| rs144517634 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959518 | CCTAAAAGAAAGCCA[C/T]TTACCTCGCTTGAAG | 5336 |
| rs144532878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937544 | TTTTCTTTTATGATT[C/T]GGGATTTGGTGACAT | 5336 |
| rs144534812 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895030 | TTCTCCTCCCTCAGG[-/A]AAAAAACAAATGTTT | 5336 |
| rs144554626 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810924 | CTTTTGCTTCCCTCT[C/G]TAAGAGGCACCAAGG | 5336 |
| rs144598462 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889019 | GCAGAGGGCCATGTG[A/C]AGAATGAGGCCTCAA | 5336 |
| rs144603102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811290 | AGACTAGAGATCGGG[C/T]ATGTAAAACCTTTAG | 5336 |
| rs144604408 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930976 | TATTTATGATGAGTG[A/T]AAAAAGCATTTTCTA | 5336 |
| rs144618591 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956335 | GGTTCCACTTTAAGC[A/G]TGCAGCTGCTTAGAC | 5336 |
| rs144640779 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797032 | GAATTTAAGAGGCGT[A/T]GCTTTCTTCCACGTG | 5336 |
| rs144663678 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924360 | AATCTGAATAGCAGC[A/G]TGCATGGAGTGCTTC | 5336 |
| rs144667401 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824699 | GATCCTCTCGTAGCT[G/T]CCATGTGACCTCTGG | 5336 |
| rs144670927 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923074 | GGCTTGCTGAGCACC[C/G]GCACTGTGATGACAG | 5336 |
| rs144675598 | in-del | -/AATAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789125 | CGGAACTTAAAGTAA[-/AATAA]AATAAAATAAATATA | 5336 |
| rs144681025 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799229 | CAACCCCTTAGCCCC[C/T]GCCACCCCCCTACCC | 5336 |
| rs144697646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886714 | ACTTACTTAATGACT[A/G]GAAGCCTCTCCTCTG | 5336 |
| rs144704755 | in-del | -/A/G | 0.0392657 | 0.134503 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940459 | CCTTTGGCATCTTGG[-/A/G]GGGGGGAGTAACAAT | 5336 |
| rs144721148 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950098 | CAGAATAAGTTAAAG[C/G]AAGGTAAAATGTGTA | 5336 |
| rs144725417 | snp | A/G | 0.0399052 | 0.1355 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962846 | ATCCCACGTTTCTTT[A/G]GGTTACAGGTTTATC | 5336 |
| rs144731223 | in-del | -/CTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816652 | CCAGCTAATTTTAAT[-/CTT]TTTTTTTTTTTTTTT | 5336 |
| rs144733835 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921075 | CCAAAAGAAAATTCT[A/G]TGAGGTTTCAACTCC | 5336 |
| rs144769851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926521 | TGTTTTAGCTGAATA[A/G]TAATAAGAGCTAACA | 5336 |
| rs144770223 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943250 | TTATAAAGAAAAGAG[A/G]TTTGATTGGCTCACA | 5336 |
| rs144772920 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929570 | TGGCTAATTTTTGTA[-/C]TTTTTAGTAGAGCTA | 5336 |
| rs144775047 | in-del | -/AAAG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925891 | CTCTGTCTCAAAAAA[-/AAAG]AAAAAAAAAAAAAAT | 5336 |
| rs144790218 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796530 | GTGCCTGTTACGGAT[G/T]GAATTGTCCTTACCA | 5336 |
| rs144808094 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926166 | GCATGATAGGGACGA[C/G/T]GGGCCAGCTGGAGTC | 5336 |
| rs144808197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899903 | AAAATGTTGTGACCA[C/T]ACGCTCAAAAGGCCC | 5336 |
| rs144809332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900560 | CCTCTGTGGGGCAGA[G/T]GCAGAGGTGTGTGCT | 5336 |
| rs144813376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861807 | CTGAAGTCGGCTCTT[C/T]GTTTGTGAGGTCAAG | 5336 |
| rs144819752 | in-del | -/TGGGGGG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790881 | AGAGGCCAGAGAGGC[-/TGGGGGG]TGTTAAATGTTCTGT | 5336 |
| rs144820048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804782 | CCTCTTTGGCAATCA[C/G]TTACCTCCTAAGAGG | 5336 |
| rs144844439 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920655 | AGCCCTAAGGTGACA[A/T]GAGGAACAGAAAGAA | 5336 |
| rs144847310 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840049 | GTGACAGGGCATGAC[C/G]TTGTCTCCAAAAAAA | 5336 |
| rs144852909 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864709 | TGCTACAAAAGAGCC[A/G]GGGGCAGTGGAGGTG | 5336 |
| rs144863459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897883 | TACTGCAGATGTCCC[C/T]TGAGCTGGGTGGAGG | 5336 |
| rs144877284 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870601 | CAGGGGGATTAGGGA[A/T]CGTGTGGAGGGTTTT | 5336 |
| rs144897462 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901652 | TCCTTCCATTGTGAA[C/T]ATTGGCAGCAAGCCA | 5336 |
| rs144913066 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813569 | GAAGGAGATTTTTCT[A/G]TAACAGTGTAAAAAC | 5336 |
| rs144920267 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778415 | TTGGAAGTGAAATTC[A/G]AGTGCCTGACAGCTG | 5336 |
| rs144925135 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923254 | CCTAACCCTTAACCC[C/T]AACCCAGGTACCCTT | 5336 |
| rs144944138 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900828 | GGGAGCCCAGTGGCT[-/C]CGGTTCCCCGGCTCT | 5336 |
| rs144962953 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803398 | TATTATCAACACTTC[A/C]TTCCTTTTTAAGACT | 5336 |
| rs144978760 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803065 | TTTTGCCTTTACAGA[C/G]TTTCCTATTCTGGAC | 5336 |
| rs144987312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905668 | TTAAACTTTATTTAT[C/T]TATGTTGTGGGACAG | 5336 |
| rs144992361 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795404 | ATTCTGGCATAGGGC[A/T]TAGCAACAAAGCTTT | 5336 |
| rs144993952 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802215 | CCTCCCGGGTTCACA[C/G]CATTCTCTTGCCTCA | 5336 |
| rs145000127 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822073 | GCTGCAGAGATGCTG[C/T]AAATAGGGAGTGTCT | 5336 |
| rs145019156 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868331 | GCCCTTAGTGACCTT[G/T]CCTTGCTCTGAACCC | 5336 |
| rs145022395 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851722 | TTCACCTTGTTGGCC[A/C]GGCTGGTCTCGAATT | 5336 |
| rs145025126 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862701 | ATGGGGAAACCCTGT[C/G]TATACAGAAAGTACA | 5336 |
| rs145051374 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912283 | GTTGGCCAGGCTGGT[C/G]TCAAACTCCTGACCC | 5336 |
| rs145051797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955048 | TTAATAGGGAGGAAA[A/G]TCATTACTAAGTGAA | 5336 |
| rs145080817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911120 | TAGTGAAATGAGTAT[C/T]AAGGTAGGTCTTGCG | 5336 |
| rs145088743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954691 | TTTTTGTGGCTGCAT[A/G]GTATTCCATGGTGTA | 5336 |
| rs145112480 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807147 | GACCTCACAGCAGAG[C/G]CTTATCTTGTTGAAC | 5336 |
| rs145124299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914794 | TAGTTGGTGGTTGGT[A/G]AATGCTGGCTCAGTG | 5336 |
| rs145125190 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888474 | TCAGGCAGTCCACCC[A/C/G]CCTCGGCCTACCAAA | 5336 |
| rs145135545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851296 | AGTTATCAAAACCTG[A/G]ACATGGTCGCTGGTG | 5336 |
| rs145148290 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908765 | GGGTATGACTCACTT[C/T]GGCACTGTAACCCAG | 5336 |
| rs145171937 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890117 | GAACGCCCGAAAAGA[C/T]GTCTCAAAAGGCCAA | 5336 |
| rs145210218 | snp | C/T | 0.00039473 | 0.0140431 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889146 | TTCTCACTTTGCTGA[C/T]CTCTCGTTCTCTTTG | 5336 |
| rs145226626 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851671 | GCCTGTGCCACCAAG[A/C]CCAGCTACTTTTTGT | 5336 |
| rs145235264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850545 | TTGACAAGAGGTCCA[A/C]AGAGTTTTCCCAGAC | 5336 |
| rs145241180 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796032 | GGCAGCTCTAGGTGC[C/T]CCAGTGAAGGCTGAT | 5336 |
| rs145247174 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852171 | CATGGTAGACAAGGT[C/G]GTCCCTGCCACTCCC | 5336 |
| rs145249561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812629 | TTTCTTCCATTCTGT[A/G]TGTTGCCTGCTCACT | 5336 |
| rs145253120 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901167 | GACAGCCCCATGCGA[C/G]GTGCTGGAGGTGTCC | 5336 |
| rs145257566 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862215 | GGAAAGACTGAAGGC[A/G]AGAGGGGGCAGGCTC | 5336 |
| rs145266449 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913221 | CTAATGACAAGGAGC[C/G/T]GAGGAGTGACTCAGA | 5336 |
| rs145270091 | in-del | -/C | 0.089084 | 0.191327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901221 | ATTGCAGCTTCCAGT[-/C]TGTGTGGGAGGCGGG | 5336 |
| rs145271371 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960486 | GGTTATTACAAGGAA[A/G]AATAAAGTGGGGAGG | 5336 |
| rs145318165 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795325 | CCTCTCTGTAGAGGT[A/G]ATGTTTGAGCTGAGA | 5336 |
| rs145327475 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795144 | GAACAGGACCCTGAA[G/T]ATCTCTAGAGGATCT | 5336 |
| rs145363122 | in-del | -/T | 0.473174 | 0.112665 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885624 | TCTCACAGATAGAAC[-/T]TTTTTTTTTTAAAAT | 5336 |
| rs145364512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793041 | ATTGCATAATCGAAA[C/G]TTAATACAATAAGAC | 5336 |
| rs145377423 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782067 | TTTTTTAGTAGAGAC[A/G]GGGTTTCATCGTGTT | 5336 |
| rs145398318 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931804 | GTGGATTCAGACAAT[C/T]GGAGCACCTCTTGTT | 5336 |
| rs145402250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901149 | TCCCCATCCTCTCTC[A/G]GAGACAGCCCCATGC | 5336 |
| rs145404179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943367 | ATGGCCAGCAGGAGG[A/T]AAAGAGAGCTAGTGA | 5336 |
| rs145405304 | in-del | -/GGCATGGTGGCTCACAGGCCA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957001 | AGAAATCCTTGGCCG[-/GGCATGGTGGCTCACAGGCCA]GGCATGGTGGCTCAT | 5336 |
| rs145406830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876922 | CATATGTACGTGTAG[A/T]GTGGGATGCTAGAGA | 5336 |
| rs145408536 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897585 | GAGTCTCCCTCTGTC[G/T]CCCAGGCTAGAGTGC | 5336 |
| rs145441357 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887917 | CTGTGCAGCAGCTGC[G/T]TTGGAACTGGTCATG | 5336 |
| rs145459344 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911824 | TTTTTTTGGGACAGA[A/G]TCACATTCTGTTGCC | 5336 |
| rs145469230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941629 | ACTCTAGCAATAATA[A/G]TGAGTATTCATTTGT | 5336 |
| rs145469669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954835 | AGTAGAATGATTTAT[A/G]TTCCTTTGGGTACAT | 5336 |
| rs145474830 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850955 | TCAGTGGGAATGGCC[C/G]TTTGAACAAGATTTA | 5336 |
| rs145483778 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799825 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCTCCCA | 5336 |
| rs145494459 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922065 | CTTTTCCTTCCTGTG[G/T]CCTTGGAGACTGGCT | 5336 |
| rs145500598 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879238 | GGGCTTGGAAGTGTT[C/G]TAGCCCCTGATGCCT | 5336 |
| rs145504209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951747 | TAAGCATTTATTCTG[C/G]AATGCAAGGATGGTT | 5336 |
| rs145533399 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819089 | TGCTCAAGTCTACAC[A/G]GCGGGGCATGGCAGA | 5336 |
| rs145536584 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879813 | GAAGCTGGAGGGAGG[A/G]GTGCTCCATGGCGCC | 5336 |
| rs145549246 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927536 | TTGAGAACGTGCTTG[C/G]GGCGAGTAAGCAAGT | 5336 |
| rs145552842 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840861 | TTGGGGGTGGATCCA[C/G]CTAGAACAAGATGAA | 5336 |
| rs145552899 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815944 | ACTTGCGCCTGTAAT[C/T]CTGGCTACTCAGGAG | 5336 |
| rs145585090 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923937 | ACCAAATCTTCATTA[C/T]TCCCTGTGACAAAAG | 5336 |
| rs145590761 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797832 | TCAGTTTTCTTTTTT[C/T]TTGTCTTTTTTTTTT | 5336 |
| rs145593478 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803531 | TTCTTTCTTTCCTTT[C/T]TTTCTTTTCTTTCTT | 5336 |
| rs145604853 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878661 | CACTTCATCTTGGCA[C/T]GTCAGCCATCACCTC | 5336 |
| rs145613958 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785326 | GGCACAGAGAGGTCA[A/G]GCAGTCTACCCAGAG | 5336 |
| rs145638746 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842012 | CCCTCCTGGGGCCAC[G/T]TGATTTTTATTTCAT | 5336 |
| rs145694307 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946679 | CATAAATTAATCACC[C/T]CCCAAGCTGAGCATT | 5336 |
| rs145702511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793034 | GGGAAATATTGCATA[A/G]TCGAAACTTAATACA | 5336 |
| rs145736388 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818301 | AGTCTCTCATTCCAT[C/T]GTGCTCTTCTCTTTG | 5336 |
| rs145742649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785152 | GTGAGAGAGTCCACG[A/C]AAGGATTCCTCCAAG | 5336 |
| rs145748878 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824071 | GTCCTGTCCTGTCCT[G/T]TCCTGTCCTGTCCTG | 5336 |
| rs145749174 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887872 | AATATTATGCATTCT[C/T]TTTTTAAAGGGTTTC | 5336 |
| rs145753623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914831 | TCAGCAAGGATGGCC[A/G]CTCCCCACCTCACCC | 5336 |
| rs145759368 | in-del | -/AG | 0.308908 | 0.242961 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781093 | ACAGCAAGAACACAA[-/AG]AGAAAAATTTGCCCG | 5336 |
| rs145766797 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880260 | AACCTGGCAGTGAGG[A/G]TATAGAAAAAGGTAT | 5336 |
| rs145769258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841896 | AGTAAGCAACGCTGG[A/G]GCTTTTTACTTAAAG | 5336 |
| rs145772846 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872959 | GGGTGACCACTGGCC[A/G]TGGGACTTTGGATGT | 5336 |
| rs145787269 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 16:81938711 | GGCATTGAACTCATC[C/G]AGTGTCACTCTAGAA | 5336 |
| rs145806350 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928001 | TTTGGGGTGGTGCAG[A/G]CAAGGAGTGGATGCC | 5336 |
| rs145825702 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909410 | TGAAAGAGGGAAATT[A/T]TAATTCTGTCACTTA | 5336 |
| rs145825783 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935073 | TTAGTTCTTACTGCC[A/G]TTACCACAAACTTGG | 5336 |
| rs145837627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868549 | GTAGGAGTCTTGTTC[A/T]TCCATTCATGTGTGT | 5336 |
| rs145838332 | snp | C/G | 0.000718795 | 0.0189441 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870947 | ATCGGTAAGATGATT[C/G]TTGAGCAAGTGATCA | 5336 |
| rs145841372 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825355 | GTGCAATGGCATGAT[C/T]ACAGCTCACTGCAAC | 5336 |
| rs145846099 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815914 | TAAAAATACAAAAAT[A/T]AGCCAGGCATGGTGA | 5336 |
| rs145853182 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911573 | CTCCTATCTGGGACT[C/G]CAGGTGTGTGCCACT | 5336 |
| rs145862737 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856440 | CTTAACCACTCCTCA[A/G]TGCCGCTTATTAACA | 5336 |
| rs145865164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851160 | CACCCATAATTGAGA[A/G]GTGTCTTTAGTTACT | 5336 |
| rs145869612 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878436 | ACTTGGACATATATT[A/C]CCGGGGACACCATCC | 5336 |
| rs145924781 | in-del | -/GGGGG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846197 | GAGGTTGTAGTGGCT[-/GGGGG]GTAAGCCAAGCCAAT | 5336 |
| rs145929773 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920134 | GCCCAGGTGGGGGTA[C/G]AGCTAAATAAGGATG | 5336 |
| rs145967895 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807280 | GAAAGGGCAGGGTGC[C/T]TTGGTAACCCTTCTG | 5336 |
| rs145970850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922235 | TTGCTTCTTATGAAA[C/T]ATCATGCACTATGGC | 5336 |
| rs145970858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894234 | AAGAGTTTGAGACCA[A/G]CCTGGGCGACATGGT | 5336 |
| rs145976625 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856216 | GGGAAGATGAGAGCA[A/G]CAGTCTCTGCCATGG | 5336 |
| rs145992734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836216 | CCAATCCCTGCATTT[C/G]TCAGAGGGGGAAACT | 5336 |
| rs146000413 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801053 | AAAGCTTGTCCCAGT[A/G]ATGCCTTGATTTTAG | 5336 |
| rs146038728 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780704 | CATTGGGTAGAGTCA[A/C/T]TGAAAAGCTGCTGGT | 5336 |
| rs146041762 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951506 | TTTTGTCTTCATTTA[A/C]ATAACGTAATTCCAA | 5336 |
| rs146069871 | snp | G/T | 1.66156e-05 | 0.00288228 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893840 | CTCGCAGCAAATTGA[G/T]GATAACCATGTGGTT | 5336 |
| rs146070662 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907211 | CCCAGCCTCCTCTCA[A/C]ATTAACGTCATGCAT | 5336 |
| rs146079605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849475 | TTCAAAGATCCCCTC[C/T]TGGCTGGGCGTGGTA | 5336 |
| rs146089618 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886341 | GCCATGAGCATCCAT[A/C/G]CGATGTTTGTTGGTC | 5336 |
| rs146093305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909706 | GCTGTAAGCCATTGC[A/C]CCTGGCTGAAAATTA | 5336 |
| rs146095053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953347 | TGTACTGTGGTTGTG[C/T]GAGATGTTAACACTG | 5336 |
| rs146097427 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883667 | CCCTCACCTGGCTGG[A/G]TGCACCTTTTCTGGC | 5336 |
| rs146098539 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846860 | CTCTTTCCTCTTCCC[C/G/T]CTGTACTCAACACTT | 5336 |
| rs146118032 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826550 | TGTAACAAGCACTTA[C/G]AATAACACATGTTCA | 5336 |
| rs146121300 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794739 | TATTTTTTGCTCTTG[A/C]TGTCGTTGATGTCAT | 5336 |
| rs146124551 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792761 | ACAGCATGGAGGTAA[C/T]CGGCCCTATGATTCA | 5336 |
| rs146125636 | in-del | -/TAAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789122 | TCCCGGAACTTAAAG[-/TAAAA]TAAAATAAAATAAAT | 5336 |
| rs146147903 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959854 | CACAGCAGAGCTCAG[C/G]TGTTGCTGTCATTAC | 5336 |
| rs146153806 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935855 | ACCATTCCCATTCTC[C/T]CTCTTCTATAACTGT | 5336 |
| rs146161780 | in-del | -/GTAA | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936599 | GCAGGCTTCGTGATT[-/GTAA]GTAAGTGACAGAGGC | 5336 |
| rs146168517 | in-del | -/T | 0.499776 | 0.0105807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870769 | ATGCCATTTCTGAAA[-/T]CAAAAATTATTCTAT | 5336 |
| rs146175110 | snp | A/G | 8.28384e-05 | 0.00643524 | missense | PLCG2 | GRCh38.p7 | 16:81940036 | TTGCTCATGCCACTT[A/G]CCCCATTAAAGCAGT | 5336 |
| rs146192510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897233 | GGCAAGAGGCCTTCT[A/G]TAGGCTCATTGGAAT | 5336 |
| rs146216356 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942664 | TGAAAGGGGTTTTAT[A/C]TTTGGTTTTAAAATT | 5336 |
| rs146218455 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876703 | TTTCTCCTGACCTCA[C/G]TGGCCCTTTGCTGGG | 5336 |
| rs146220031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900272 | GGTGCTTATTGTGCT[A/G]TCTGTTCATCTTTTC | 5336 |
| rs146220227 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834791 | CCTTTAACAAAACCT[C/T]CTGCCAGTCCCCAGA | 5336 |
| rs146223164 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791426 | TAGATCTGGGCAGAG[C/T]TCAGCTGGGCAATTC | 5336 |
| rs146237377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857315 | TCTGGAGTTGGACAC[C/T]TGGGTTTGAATTCCT | 5336 |
| rs146237620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816864 | TGAAAGTGCGGTTGC[A/G]CTGTTATCATTAGTG | 5336 |
| rs146256355 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815463 | GGCTGAGAGACCACC[C/G]CCTAGAGGCTTCCTC | 5336 |
| rs146265147 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800740 | CGCTCTCTGCTCCCA[A/C]GATGCCCTTGTCTTA | 5336 |
| rs146268893 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948636 | GGGAGCTGCACTCTG[C/G]CACTGAGCTGGTCCT | 5336 |
| rs146292109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928929 | CTGTGTTTCCCATGC[A/G]TTGCGAAGGAAAGCT | 5336 |
| rs146317930 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869485 | GTCTCAATCCTAGCA[A/G]AGAATGTAATCAATA | 5336 |
| rs146324903 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855511 | ATAACTTATTAATTT[A/C/G]TCATTCATTCTTTTA | 5336 |
| rs146332745 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930863 | TTCACAAAATTTTAT[A/G]TATTGTATGTAAACA | 5336 |
| rs146357769 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849136 | GCTGTGGTTCTTAGT[C/T]CTTACAGCAATGGGA | 5336 |
| rs146359617 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809743 | CCCCTGATTGGCTAG[C/G]CTTGTCACTTCTGTC | 5336 |
| rs146359883 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789546 | CTCCCACCTTGGTCT[A/C]CGAAAGTGCTGGGAT | 5336 |
| rs146376124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846638 | AATGCTTAAAAAGAT[C/T]ATGAGTAGATAGTCC | 5336 |
| rs146378438 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808249 | AGCCTGTTTTCCAAC[G/T]GGGCTACACTGTTTT | 5336 |
| rs146385550 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792353 | TGGGTGTAGTGGCAC[A/T]TGCCTGTAGTCCCAG | 5336 |
| rs146405138 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962085 | GAGGACGACCAACCC[C/T]GATAGAGGAGGACCG | 5336 |
| rs146413296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892406 | CTTATTGGGTGAGGG[A/G]TGAAGTCCTTGGGTG | 5336 |
| rs146421993 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918984 | TGGGGGGGATTGGCA[A/G]ACATTTTCTGTGAAG | 5336 |
| rs146434709 | snp | A/G | 4.97558e-05 | 0.00498753 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854437 | GCTCATGTTAATTTC[A/G]TTTTAGTGGATATCA | 5336 |
| rs146442518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831544 | GGGTTAGTATTTGAA[A/C]CTCATCCAACCCCAT | 5336 |
| rs146443035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799627 | TTTTTGAGACAGAGT[C/G]TCGCTCTATTGCCCA | 5336 |
| rs146453927 | in-del | -/GTGTGT | 0.495891 | 0.0451408 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830648 | AAAAAAATGTGTGGG[-/GTGTGT]GTGTGTGTGTGTGTA | 5336 |
| rs146466566 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895364 | AGGAGATTGAGACCA[A/C]CCTGGCCAACATGGT | 5336 |
| rs146473018 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948719 | ACAAAGGCCCTCCTT[A/C]TGCCTCATCAGCTAA | 5336 |
| rs146473829 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830074 | CCTATAATCTCAGCA[C/G]TTTGGGAGGCTGAGG | 5336 |
| rs146476394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857053 | TTAGACTTCTGGCCT[C/G]TCTAACAGTCTGAAA | 5336 |
| rs146477440 | in-del | -/AGGG | 0.18316 | 0.240899 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930639 | GTGGTCTCAGCTACT[-/AGGG]TAGGGAGGCTGAGGT | 5336 |
| rs146503142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822142 | CCCTAGAGCTTGTTA[C/T]CAATTTCTCTTAGCT | 5336 |
| rs146513916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883978 | GCGGGAGGCTGCTGC[C/T]GGCATCTAGCAGGTC | 5336 |
| rs146514016 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863058 | ATGAAACATAGAACA[A/T]CATTGATCATTTTAA | 5336 |
| rs146517508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882616 | GCAATCCCTCCCTCT[A/G]GCCTGCGTTCCCTCG | 5336 |
| rs146530022 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925983 | GCTGCTTGGATGACT[G/T]TGGGGACAGGATGCC | 5336 |
| rs146540526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788205 | AAAGGGTGATCGTTG[C/T]ATTATTCTTCATTTG | 5336 |
| rs146553414 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962196 | CCACTAAGTGATGAA[G/T]TGTATTTGGAAGCAA | 5336 |
| rs146557294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844435 | CAAGTGATTCTCCTG[C/T]CTCAGACTTCCTAGT | 5336 |
| rs146565612 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823616 | CTGTAGCCTCAAACT[C/T]CTGGGCTCAAGCGAT | 5336 |
| rs146567504 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790286 | CTGGAGGGGAGTAGG[A/G]TCCATTCTCAGGTTT | 5336 |
| rs146584498 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822002 | CCTTCTCTTTTCCTG[C/T]GTTAACTAGGGAAGA | 5336 |
| rs146612110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935378 | TGCCATATAAAGTGA[C/T]ATGCACAGGCTCCAG | 5336 |
| rs146630005 | snp | A/C | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889772 | TGATTCTCGTGCCTC[A/C]GCCTCCCGAGTAGCT | 5336 |
| rs146630092 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916935 | GAGCCACCACGCCCG[G/T]CCAGGACTTTGTTAT | 5336 |
| rs146635453 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852229 | AGCCGTGGAGGGGAG[A/G]TTTTACCAGTAGTCC | 5336 |
| rs146648268 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914551 | TTCCCCATGAGATTG[C/G]AGGTGTCTTGAGAAT | 5336 |
| rs146675777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831895 | GGGGAAATGAAGGGC[C/T]GGCTTGCTAACCACA | 5336 |
| rs146682485 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813433 | ATTCTCTTAGTAGCA[A/G]TTGTGAATGGGAGTT | 5336 |
| rs146714346 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944814 | ACTTGAGCCTCCAAG[C/G]ATTTTGGTATCTGGG | 5336 |
| rs146754291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880604 | ATGTACGTAAATGTT[A/G]TAATATGATATGATA | 5336 |
| rs146754883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842278 | GAGAAGCCTTTCTTC[C/T]CCTTGCTGGGGAGGA | 5336 |
| rs146758757 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903231 | GTGGTGGTGTCAACA[C/T]GTGGCATGTACCCTA | 5336 |
| rs146762754 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801839 | TTGTACACCACCACG[C/G]CTGGTTAATTTTTGT | 5336 |
| rs146770710 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946764 | TTTTTCCTCCTTTAC[A/G]CCAGAATTCTTTCCT | 5336 |
| rs146780901 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805287 | GATGGATCACAAGGT[C/T]AGGAGATCGAGACCA | 5336 |
| rs146782318 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800505 | TTTGCTGAGGATGAT[A/G]GCTTCCAGCTTCATC | 5336 |
| rs146806571 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806615 | AGGATAGCCTGCAGA[C/T]ATGTGATTCGTGTCT | 5336 |
| rs146832381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932096 | AATCAGCGAGACCCG[A/G]TTCTTTCCGGTGGAG | 5336 |
| rs146832842 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960190 | CTTGACAGAGTAACA[C/T]GTTAATCTGGTTCTT | 5336 |
| rs146848625 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787546 | CACTCTTTTTTTTTT[G/T]TTTTATAATAGATTG | 5336 |
| rs146851902 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958582 | GAGTGATGGGATCTG[C/T]TCATTAAGACAATTT | 5336 |
| rs146871607 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937182 | TCGTGGGCGGGGATG[C/T]AAATAGGTGGAGGTT | 5336 |
| rs146875009 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872860 | GCATTTTTAAGTGAT[A/G]AGCATGAATGTTCCT | 5336 |
| rs146877191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829516 | AGCCACCACACCCGG[C/T]CCATTTCTCTGTTTT | 5336 |
| rs146877379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894534 | TGGCTATTTTCCTTC[C/T]GGCCTCTCTCTCACC | 5336 |
| rs146890635 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934849 | GAGAGAGAATGAGAA[C/G/T]CAAGTGAAAGGGGAA | 5336 |
| rs146904035 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926484 | CCCGTGTTGTTAGTG[C/T]TGTTATAAAGATAGG | 5336 |
| rs146904968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950039 | GGAGGAAAAAAGGAG[A/T]TCAACATAAACTTGA | 5336 |
| rs146913733 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779167 | CGCGGGGACGCTGCA[C/G]TCGGGGTGCGCTCCG | 5336 |
| rs146924869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845624 | CTGCACTAGAATCTT[G/T]TTCCCAGCCTCGGGT | 5336 |
| rs146938396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906671 | TCAAGTGGTCTGCCC[A/G]CCTTGGCCTCCCGAA | 5336 |
| rs146939837 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949754 | TATCAAATAAGGATT[C/T]TTGAATTGGAAGAAA | 5336 |
| rs146946587 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884824 | ACATACACAAAAGCA[C/G]ACAGACGGTTTAATG | 5336 |
| rs146947635 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848626 | CCTCTCTGTCCCCTG[C/G]TCTGCTCAGTCATCA | 5336 |
| rs146948024 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822527 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA | 5336 |
| rs146962963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882942 | ACACTGTATCCCATA[C/T]GCCTGGTTCACCTGT | 5336 |
| rs146970891 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793304 | GGTTTTCTTTCCTTT[C/G]TGAGGGACCTAGTTG | 5336 |
| rs146987248 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791621 | CCAGGCTGGAGTGCA[A/G]TGGTGCAGCCTCGGC | 5336 |
| rs147007515 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916370 | TCTCTATAGTGCAAA[A/G]AATGCCTTTTCTTGA | 5336 |
| rs147045716 | snp | A/G | 0.014503 | 0.0839134 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938955 | TGCTTTTAAACGTCC[A/G]GCCAGTGAATCCTTT | 5336 |
| rs147055016 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835980 | ATGAGCTCATCTTGA[C/G]TACATCTGCAAAGAC | 5336 |
| rs147066842 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898025 | CTTCTAAGTGCCAAC[C/G]TCCATCAGGCAGATG | 5336 |
| rs147093084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779978 | ATGCGTGTGTCTGTG[C/T]GTGTTGTGTTTTGTT | 5336 |
| rs147112036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904008 | AAGACACTGCAGGAC[A/G]AATAACCTCAGCCCT | 5336 |
| rs147112751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947511 | ATGCCCACGGTCATA[C/T]CTTTTATTTATCACC | 5336 |
| rs147135703 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804470 | ATATGTTAGCTTGCA[A/G]CACATGGGCATGGAC | 5336 |
| rs147147687 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941577 | GATTTTTTTTTTTTT[-/TT]GTACTCTAGAAATGT | 5336 |
| rs147151253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863735 | ACACTTACTTCCTTT[C/T]CCTCCTCTGCCCTTG | 5336 |
| rs147152315 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823231 | AGGTCTGGCTTCCCC[A/G]GGGCTTTACCTCGAG | 5336 |
| rs147152679 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803069 | GCCTTTACAGAGTTT[C/G]CTATTCTGGACATTT | 5336 |
| rs147162703 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957174 | CATGGTCGTGGGCGC[A/C]TGTAATCCCAGCTAC | 5336 |
| rs147178971 | in-del | -/T | 0.254385 | 0.249962 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884708 | CTTTTACTTCATTTG[-/T]TTTTTTTTTAAATAG | 5336 |
| rs147185577 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959362 | AACAAATCAGGCTCT[C/G]ACCAGAAGATCCTTC | 5336 |
| rs147186059 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931046 | AAGACGAACACATGT[C/G]TATAACTAAAGTGGA | 5336 |
| rs147201176 | snp | C/T | 0.00052223 | 0.0161506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889151 | ACTTTGCTGATCTCT[C/T]GTTCTCTTTGTCATT | 5336 |
| rs147222180 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933040 | TTAATGTGGAAAAGT[A/G]TTATTTCCCTAGAAG | 5336 |
| rs147226046 | snp | A/C/T | 0.41507 | 0.187755 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778063 | AAAAAAACAAAAAAA[A/C/T]CCAAAAACACACACA | 5336 |
| rs147245934 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795214 | CATTCAATCATGTTG[G/T]ATCGTGATAGACGCT | 5336 |
| rs147246644 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813137 | TGTTCTTTCTGCTTA[A/G]GGTTGTCTTGGTTAT | 5336 |
| rs147266556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946428 | CTAATTCCCCAGAGT[A/G]TCCTGGGTTTTCCCT | 5336 |
| rs147279894 | snp | A/C/T | 0.0252962 | 0.110012 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798830 | GGCTGGCCTCCCCGG[A/C/T]CTCAGGACTTCAGGG | 5336 |
| rs147289612 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947908 | GTAGATTTCCATTGC[A/C]TTATGATTTTTTGTA | 5336 |
| rs147306423 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879925 | ATTTCTTTCGTCTTC[C/T]TGCCTTCGAAGATTA | 5336 |
| rs147313494 | snp | C/G/T | 0.00295153 | 0.0383026 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883221 | CTCCTCTCGACTCCT[C/G/T]TGTTGAATGTGTCTG | 5336 |
| rs147326110 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925241 | CTCTCTGATGGCAGT[A/G/T]GTGCTACCTAGGGGG | 5336 |
| rs147330136 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881916 | CTTGGCCTCCCGAAG[C/T]GCTGGGATTACAGGC | 5336 |
| rs147348398 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820508 | GTAGTTTTTCCTTTT[C/G]TGTTGCTGAGCAGCA | 5336 |
| rs147349332 | snp | A/C | 0.000397443 | 0.0140913 | missense | PLCG2 | GRCh38.p7 | 16:81786099 | GCTTCCGCAAGTCCA[A/C]CCCCGAGCGGAGAAC | 5336 |
| rs147364981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817110 | GACGGATGGTAAACA[A/G]GGAGGTGAAGACAAA | 5336 |
| rs147373352 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933791 | CCAATAAAAGTCTGA[C/T]AGAATTTGGGGAGGC | 5336 |
| rs147385460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788838 | CTGTTTGCATTGGCC[A/G]GCTCCACCCCCAGGT | 5336 |
| rs147395243 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935974 | AACTAGGCCCCTTTT[C/T]AATACTTGGAACCCC | 5336 |
| rs147396004 | snp | C/T | 0.00256573 | 0.0357251 | missense | PLCG2 | GRCh38.p7 | 16:81910645 | AGCACTACCGCGAGA[C/T]GCACCTGCGCTGCGC | 5336 |
| rs147406608 | snp | A/C | | | missense | PLCG2 | GRCh38.p7 | 16:81908589 | CTACACCCTGTCCTT[A/C]TGGTAATGCCCCCGA | 5336 |
| rs147418247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851616 | CTCCCGAGTTCAGGC[C/G]ATTCTTCTGCCTCAT | 5336 |
| rs147418552 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875732 | TGTGGTTACAGCATT[C/G]TTACATAAAAATAGA | 5336 |
| rs147431697 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912832 | CCCTGCCCCCCCAGC[A/G]TCAGCGACAACAACA | 5336 |
| rs147434904 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874231 | AGATCTGGCTATAAA[C/T]AGGGTCACATCTCGC | 5336 |
| rs147468519 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873730 | AGCTCAGGAGTTTGA[C/G]ACTAGCCTGGGCAAC | 5336 |
| rs147468764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810802 | GTTCTGATAGAAGGA[G/T]ACAGGGTCTTTAATT | 5336 |
| rs147470120 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830410 | TTCTTGGGTTCAAGC[A/G]TTTCTTGTGCCTCAG | 5336 |
| rs147478284 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925704 | ACCAGCCTGGCCAAC[A/C]TGGTAAAACCCTGTC | 5336 |
| rs147482595 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778044 | AAACAAAAAAAAAAC[A/C]AAAAAAAAAACAAAA | 5336 |
| rs147496783 | in-del | -/TC | 0.234055 | 0.249491 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813764 | TTCCTTTGTGCAGCG[-/TC]TCTCCCTGTTCTGTG | 5336 |
| rs147501175 | snp | C/G | 3.49534e-05 | 0.00418037 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900784 | ATCATCATCAAGGTA[C/G]GCACCCCGGGTGCTG | 5336 |
| rs147525931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840752 | CCTAACGGGCCACAG[A/G]CAGGTGCCAGTTCAT | 5336 |
| rs147537701 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902349 | AGGAACTGATTTCTC[A/G]CGGTTCTGGAGGCTG | 5336 |
| rs147540301 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805072 | GGAACAACATCAGAC[A/T]CTTTTCCCCAATCAC | 5336 |
| rs147549717 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952238 | GAATTGGAGGTATCA[A/G]TATAAACTCAAGTTA | 5336 |
| rs147554621 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908877 | AAACAAAGACAAGAT[C/G]TGACCCTACTCTTAG | 5336 |
| rs147564956 | in-del | -/G/GG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940457 | GACCTTTGGCATCTT[-/G/GG]GGGGGGGGAGTAACA | 5336 |
| rs147587654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887361 | CCTGACCTCATGATC[C/T]GCCCACCTCGGCCTC | 5336 |
| rs147589647 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884916 | TGAGATAAGGTCTCA[C/T]TCACCCCCTTGCCCA | 5336 |
| rs147601278 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954709 | ATTCCATGGTGTATA[C/T]GTACCACATTTTCTT | 5336 |
| rs147623410 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825236 | GGAGTGTGTTTTTTT[A/C]CTATTACTGCTCTAA | 5336 |
| rs147629972 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808592 | TCCGCCTCCCAGATT[C/G]AAGCCATTCTCCTGT | 5336 |
| rs147646042 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870043 | TTTTGTATTAATGAG[C/T]TCCTGGAAAAATTAT | 5336 |
| rs147646630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827158 | TGTGGTAAGGTGCAT[A/G]GTTAATCTCATACAT | 5336 |
| rs147654781 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941788 | TGTAACCTCTGCCTC[A/C]GCCTCCTCAGTAGCT | 5336 |
| rs147687666 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921001 | GGCCTCTCTGATTTT[G/T]GGTTAGTTTCCAAGT | 5336 |
| rs147703351 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943777 | AAAATCACATTGTAG[C/T]GATAGGGAAAAATAG | 5336 |
| rs147713839 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800014 | TGGCTATGCCACTTA[A/T]CCCATTTGTGGCCAT | 5336 |
| rs147726716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856850 | TCTAGTGGAATCACA[A/G]GGGTTCTTAGATACC | 5336 |
| rs147734877 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801639 | ATTTTTTAAAAACCT[A/G]TCTCCCATTTTTTCG | 5336 |
| rs147749022 | snp | C/T | 0.00107795 | 0.0231908 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859113 | TCTCATATTTCTTTC[C/T]AGTTGGCTGAGAAAG | 5336 |
| rs147759171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929964 | CTTGGAGTCAGGTTT[A/G]AACTGAGCCTCAGTT | 5336 |
| rs147797768 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870490 | AAGGAGGAGTTACGC[A/G]TCATGTCTCTTGGAA | 5336 |
| rs147808808 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906477 | TTGCCCTGGCTGGAG[A/T]GTGGTGGTACGATCT | 5336 |
| rs147809234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931296 | TCTTTTCGGAGGACC[C/T]TACTGAATCTACTGC | 5336 |
| rs147817611 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791495 | CACCTCGCCTGGAAG[G/T]TTCCAGAATCTTCAC | 5336 |
| rs147819000 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810993 | CGAAACTGATCTAAC[A/G]GTGGCCTTCCTGGCC | 5336 |
| rs147830709 | snp | G/T | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872264 | ACCTGGGAGGCGGAG[G/T]TTGCAGTGAGCCGAG | 5336 |
| rs147833512 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848231 | CACTCAGTGGAGAAA[G/T]GATAATCATTTCAGA | 5336 |
| rs147835355 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808610 | GCCATTCTCCTGTCT[C/T]AGCCTCCTGAGTAGC | 5336 |
| rs147840666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793050 | TCGAAACTTAATACA[A/G]TAAGACCAGAAAGAA | 5336 |
| rs147866543 | snp | C/T | 0.0111196 | 0.0737302 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963103 | CTGACCCCCAACCCC[C/T]AGCCCCCAGTGGTTG | 5336 |
| rs147868758 | snp | G/T | 8.02311e-05 | 0.00633317 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921346 | CTTGTTCCCATGGCA[G/T]TTATAACAGGGCAAG | 5336 |
| rs147898338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897897 | CTTGAGCTGGGTGGA[A/G]GTGTTGCTGTGAGAC | 5336 |
| rs147905221 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895531 | TGCCACTGCACTCCA[A/G]CCTGGGCAACAGAGC | 5336 |
| rs147914732 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923188 | ACCCTAACCCTAAGC[C/T]TAACCCTAACCCCAG | 5336 |
| rs147939423 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861845 | TACCACCCTCTTGCT[C/G]AGGAGGCATTCTGGC | 5336 |
| rs147941308 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801861 | AATTTTTGTACTTTT[A/G]GTAGAGACGGGGTTT | 5336 |
| rs147948428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781527 | ATTGCAGGATCGAAG[C/G]ATATGCGTGTTTTGC | 5336 |
| rs147963598 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838240 | TGTAGGCACCTGCCA[C/T]CATGCCTGGCTAATG | 5336 |
| rs147984797 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924847 | GGCTCCCAGACCCAG[C/G/T]TGGGCAACCACAGTG | 5336 |
| rs147990934 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807443 | GCATTTTTTCAGCTT[C/T]ATACAAGGCAGGAAG | 5336 |
| rs148022573 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939445 | CAACTCAGATGCTGA[C/G]CAAATAAACTGGCAT | 5336 |
| rs148042107 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842629 | GTGGTGCCCCTTGAG[G/T]TCATGTATGGGAATT | 5336 |
| rs148042803 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805478 | CACTTCAGCCTGGGT[A/G]ACAGAGCGAGACTCC | 5336 |
| rs148063117 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834064 | GACTTACCTTGTCTC[A/C/T]GGGCCTTCCACTGTG | 5336 |
| rs148066456 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785907 | AAACCCCTTTCAGTA[A/C]TAAAATCAGTTCACT | 5336 |
| rs148072397 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876111 | GCTCACTGCAGCCTC[G/T]AACTCCCTGGCTCAG | 5336 |
| rs148074163 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915376 | GCTTTCAAATCCACA[A/G]AGGAAGTGTTGAGTT | 5336 |
| rs148076046 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958948 | GCTTTAATGGGCTAA[G/T]CATTAGGGTGTTACA | 5336 |
| rs148100760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796539 | ACGGATTGAATTGTC[C/T]TTACCAATTTCATAT | 5336 |
| rs148103299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779986 | GTCTGTGCGTGTTGT[C/G]TTTTGTTGTGTTTTG | 5336 |
| rs148111026 | snp | C/G | 0.0759472 | 0.179459 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828038 | GAGCTTGCACTGAGC[C/G]GAGATCATGCCATTG | 5336 |
| rs148113673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853166 | TGAAACCCCATCTCT[A/C]CTAAAAATACAAAAA | 5336 |
| rs148117859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836049 | ACTGGACTTCTATGT[A/T]TGTTTTTGGGGGATG | 5336 |
| rs148120124 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802062 | TCTGGAATGAAAAAA[C/G]TAGAAGTTAGCTCCT | 5336 |
| rs148124361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890625 | GGGTGCTTGCTGGTC[A/G]GAATGGTTGCCTTTG | 5336 |
| rs148161999 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869019 | CCCATGTCCATGGAC[A/G]TTGCTTGAGCCTTGC | 5336 |
| rs148166959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826279 | TGCTTCCCTCTGCCA[C/T]GGCAAGGCTCCAGGA | 5336 |
| rs148179883 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930452 | TGTGTCTGCATCTGT[G/T]TTTAAAGCCATTTAG | 5336 |
| rs148200008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945445 | GAAAGATACTGTTAA[C/T]CATGGTTCCTTTTAG | 5336 |
| rs148204381 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792181 | TCCATTCTTATGGTG[C/G]TAATAAAGACATACT | 5336 |
| rs148215775 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882738 | CCTTCTTGCTCACCC[A/C]ACCTCATTCTTGCTC | 5336 |
| rs148236401 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919792 | TAGGTCCTGGGGATA[C/T]AAATTGAGCACAACA | 5336 |
| rs148237648 | snp | A/C | 0.0973687 | 0.197999 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878028 | GCTCTGTCACCCAGG[A/C]TGGAGTGTAGTGGCG | 5336 |
| rs148238991 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863375 | TTGTAGCATGTGTTA[A/G]AATCTTCTTCCTTTT | 5336 |
| rs148250391 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942506 | CATTGAGGGTCTTCC[A/G]TACTGAAAAAATAAA | 5336 |
| rs148256109 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822492 | CTGGGGGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 5336 |
| rs148278838 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803874 | TTTAATACAGACAGG[A/G]TTTCACTATGTTGGC | 5336 |
| rs148288482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935645 | CAGCATGTTGACTGC[C/T]GGGCTATCCCACCAC | 5336 |
| rs148323530 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811944 | CTCGAGGAATTGCAA[C/T]GCTGTCTTCCACAAT | 5336 |
| rs148326196 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873426 | GTGTCATTGAACATA[C/G]AACATGTCATAGAAT | 5336 |
| rs148329019 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816249 | GGCAGCACATGCCTG[C/T]AATCCCAGCTACTTG | 5336 |
| rs148337816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912443 | CTCTTTGCTGAGGTG[C/T]CTTTGTCTGGGGAAG | 5336 |
| rs148365726 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798418 | GGTTAAGTGCTCTTG[G/T]ACCTGAGCCTGGATA | 5336 |
| rs148374155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848942 | TGAGCTGAGACTGGA[A/T]GGGAGAGCTTGGCAC | 5336 |
| rs148384010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952994 | GCAGGTTGAAATCAC[A/G]TACTTCCTGAGGTGA | 5336 |
| rs148386639 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909128 | CCCTGTGCTAGACAC[A/G]GTACTTATGCCAGAC | 5336 |
| rs148393412 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861550 | TCTCATCCAAAATGC[A/C]CTGCCTGCTCCGCCA | 5336 |
| rs148429454 | snp | A/G | 0.040671 | 0.13668 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837424 | GCTTATCAGGAGGCT[A/G]CATGAACATCTATTT | 5336 |
| rs148431691 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803043 | CCCTGGCAATGACAA[A/C]TCTACTTTTTGCCTT | 5336 |
| rs148437301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892096 | GAGCAGGTGGTAAGG[C/G]AAGGAGAAGTGTTTC | 5336 |
| rs148437842 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934025 | GATAGAGAGTTATGA[C/T]GAGGATGCTGGGGTC | 5336 |
| rs148476435 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869886 | GAGACAATGGGCACC[A/G]ATTTTTGCTTACAGG | 5336 |
| rs148491296 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930989 | TGTAAAAAGCATTTT[C/G/T]TAATTGGTCAACCAA | 5336 |
| rs148500949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824716 | CATGTGACCTCTGGC[C/G]TTTTTGTCCTTCCCC | 5336 |
| rs148510738 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946699 | AGCTGAGCATTTAGA[C/T]GGAATCCATTTACAA | 5336 |
| rs148512334 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886816 | GTGTGGGGCCGAGTA[C/T]AGAGTCAGTGCTCAG | 5336 |
| rs148529019 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883415 | GTCTCACCCTTCTGC[C/T]GCCTGTGCTCACCTG | 5336 |
| rs148551879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864758 | GGCTGGTAAGTGTCA[C/T]GGGGCTGCCATCCTT | 5336 |
| rs148552139 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823439 | TGAAGATTGAGTGGG[A/G]GTAGGGGCTGCACTG | 5336 |
| rs148557181 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920736 | GCTAGTAAATGTTCA[A/G/T]ACAGCTCTCAGCGGG | 5336 |
| rs148559002 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962100 | CGATAGAGGAGGACC[A/G]GTCTTCGGTCAAGGG | 5336 |
| rs148565671 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926557 | GAGTATTTACTGTGT[A/G]CTAGGTAGGCGCTGT | 5336 |
| rs148587431 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804873 | AGCTTGGGAGCAGTA[G/T]TGAGCATCTGCCATG | 5336 |
| rs148592949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894982 | CAACGTTTTGTAGCA[G/T]TTACTCTATAGACTT | 5336 |
| rs148600529 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879580 | ATGACGTCCTGGGCT[G/T]CAAGGAGTTCAGCAA | 5336 |
| rs148609222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937137 | ACGTGCCTGAGCTAA[A/G]CCACACTGCCAAACT | 5336 |
| rs148632079 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851788 | AAAGTGCTGGGATTA[C/T]AGGCGTGGGCCACCA | 5336 |
| rs148636731 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801371 | TAATATGTTTTGCAG[C/G]TCTTTACATAAAAGA | 5336 |
| rs148641109 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817021 | GACGGGCACTGGATG[C/T]GTTAGATGCTGGGGA | 5336 |
| rs148644704 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913513 | GATGCAGGCCTGTCC[A/G]TCTCCAAAGCCTAAG | 5336 |
| rs148669659 | in-del | -/CCCCCCG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781874 | GTCCTTTCCCCCCCC[-/CCCCCCG]CCCGCCCCCGAGACG | 5336 |
| rs148687012 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849902 | TAGACTTTCACTGGC[A/C]GTCAACTGGGTGGGT | 5336 |
| rs148690185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799237 | TAGCCCCCGCCACCC[C/G]CCTACCCAGAGAGAT | 5336 |
| rs148698170 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910436 | GTTGTGTGGCCACAT[A/G]TAATGTCCCCGCCTC | 5336 |
| rs148699115 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954372 | AACTTTATTCTGTAA[A/G]ATTTTACTTTAAGTT | 5336 |
| rs148708302 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847199 | ATTAAAATGATATTA[C/G]AAAAGATAAAGATGA | 5336 |
| rs148709396 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808428 | GGCTGTGTGGCCCCA[A/G]GCCCACAGCACTGAG | 5336 |
| rs148718212 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925819 | TTGAACCTGGGAGGC[A/G]AAGGTTGCAGTGAGC | 5336 |
| rs148723745 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907280 | GGTACTTTACAATAA[A/T]ACCAGAGACTAAATT | 5336 |
| rs148746786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790672 | AATGGTGTGTGACTT[C/T]TGGACAGGTGTTACA | 5336 |
| rs148759709 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882138 | TCTTTTCCCCAGGCT[C/G]CTGCAAGTGCTCAGG | 5336 |
| rs148770457 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940808 | GGCTCTCCTTAGCTT[C/T]TATATAGTTTCTCTA | 5336 |
| rs148774531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904495 | GTGCAGCCACTTGCC[C/T]GGGGTCACACAGCTG | 5336 |
| rs148780488 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794853 | TTCCTTCCTGCACCC[A/G]ATGGATTGTCCTGCT | 5336 |
| rs148793054 | in-del | -/TTTC | 0.040671 | 0.13668 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829712 | CGATATGTAGAGGTG[-/TTTC]CTTTCTTTTGAATTG | 5336 |
| rs148798010 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821063 | TGCCTGGCTAATTTT[A/T]GTATTTTTAGTAGAG | 5336 |
| rs148801129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787194 | GTTATTATTCGAAGT[A/G]ACTATCATTGTACTC | 5336 |
| rs148808866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877137 | CTGGGGCCGCTGTGG[C/T]AAGTACTGCAACTCG | 5336 |
| rs148821834 | in-del | -/A | 0.0337553 | 0.125452 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860212 | AAGTCTTACCCAGAC[-/A]TTTTTTTTTAAAAAA | 5336 |
| rs148828856 | in-del | -/T/TTCC/TTCCT/TTCCTTTCCTTTCCT/TTTCCT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803558 | CTTTCCTTTCTTTCC[lengthTooLong]TTCCTTTCCTTTCCT | 5336 |
| rs148829037 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887923 | AGCAGCTGCTTTGGA[A/C]CTGGTCATGTATATT | 5336 |
| rs148841349 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951876 | TAGAAAAAAGGTCGA[C/G]TGATCTCTATTGTAT | 5336 |
| rs148869760 | snp | A/C/G | 0.00398691 | 0.0444912 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811116 | AGTGTGCTGGGGAAG[A/C/G]TCATATGGCACCACG | 5336 |
| rs148871695 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921996 | GTAGCAAAAACTTTT[A/G]TTAGTAGTGAAGGAT | 5336 |
| rs148880759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884326 | ACTGGACTGCAGCCT[A/G]GGCAACAGAGCAAGA | 5336 |
| rs148914633 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909284 | ACATCCCTCCCTTTA[-/T]ATTGGGGGGGTTTAA | 5336 |
| rs148915052 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805418 | GCAGGAGAATGGCGT[G/T]AACCCAGGAGGTGGA | 5336 |
| rs148917110 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880321 | TGTTTTGAGAGCACC[A/T]TGGCAGAATTTATCA | 5336 |
| rs148928783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923379 | TAACCTTGGCCTGAA[A/G]CCTCCTGCTCCCCAA | 5336 |
| rs148946421 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914851 | CCACCTCACCCCATG[A/G]CCCACTGTCAGGGAA | 5336 |
| rs148951468 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801886 | GGGTTTCACTATGTT[A/G]GTCAGGCTGGTCTCG | 5336 |
| rs149001399 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831939 | TTGCACAGGCAAAGC[A/G/T]GGGGCAGGGGTGACT | 5336 |
| rs149004357 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799904 | AGCCTGTTATTAACT[A/G]TTTTAAATGTCGATG | 5336 |
| rs149016981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856683 | TAAGCCAGTGGTACT[C/T]ATCCATGGGAAGCTG | 5336 |
| rs149020018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848800 | TGGAGCTTACAGTCT[A/G]GGAAAGGAGGGCTGT | 5336 |
| rs149024324 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809099 | GCTAAGCCAGGCCTG[C/G]TCTCTCTGAGCATGG | 5336 |
| rs149033566 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908938 | CCAGCCCTGGAGTGG[G/T]TCATGTGGCTCTGGA | 5336 |
| rs149054957 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812450 | ACCAGTGATGATGAG[A/C]TTTTTTCCTACGTTT | 5336 |
| rs149078300 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795432 | TTTCCTATTAGTGAA[G/T]GTAGCCTAATTGCAG | 5336 |
| rs149079828 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942402 | TGTGAGATACTCTCA[G/T]CAGGGACCTTTCCTC | 5336 |
| rs149087626 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949371 | GGATAAATTTAAAAA[C/T]CTGGACTTCCAGCAC | 5336 |
| rs149124551 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822228 | TCCAAAACTGTCTTT[C/G]AAATAATACTCTCCT | 5336 |
| rs149128232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862659 | TGGATCGCTTGAGCT[C/T]AGGAGTTGGAGACCA | 5336 |
| rs149134360 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960812 | TAGCCTTACCCCTGG[A/G]AGTATACCAGAGCTT | 5336 |
| rs149136265 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901249 | GGGCAGTTGCTAGAA[A/G]AGGCTGAGTGCAGCA | 5336 |
| rs149177827 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839554 | TTTTATATCTAATAC[G/T]TATTTTAATATTGAT | 5336 |
| rs149195991 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81873198 | GTAATGTTGGGGGAA[A/G]CCATCTCTGTCCTCT | 5336 |
| rs149205775 | in-del | -/TTC | 0.020168 | 0.098373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826874 | TGGGTTTTTAAAAAG[-/TTC]TTCTTCTGTATCCAT | 5336 |
| rs149208558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931808 | ATTCAGACAATTGGA[A/G]CACCTCTTGTTAGAG | 5336 |
| rs149216298 | snp | C/T | 0.0364509 | 0.129988 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779035 | TGATATTGGGGAATT[C/T]CCTTTGCACCTGGCC | 5336 |
| rs149229107 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911983 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 5336 |
| rs149231444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835318 | ATAATGAAGATGGCC[A/G]GGTGTGGTGGCTCAC | 5336 |
| rs149239175 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924558 | GCTGAGATTTGAACC[A/G]CCAGGCCTTTTGACT | 5336 |
| rs149242209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881523 | GGGAGAAATGTTGGC[C/G]CTGGAGTTAATGGTC | 5336 |
| rs149261030 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959447 | GCCAAGATTTGGGGG[G/T]GTGGATGTTTAAACA | 5336 |
| rs149263393 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916824 | TGTATTTTTGGTAAA[A/G]GTGGGGTTTCACCAT | 5336 |
| rs149278622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860800 | ACACGGTAAAACCCT[C/G]TCTCTACTAAAATAC | 5336 |
| rs149282468 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820240 | ATGTGTAACCACCAC[C/G]CTAATTGAGACACAG | 5336 |
| rs149311272 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956294 | CTTTTAGTTCTCATG[C/T]CATGCTGTTTTTTTC | 5336 |
| rs149315118 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846762 | AGATACAAGAAAAGG[-/T]TTTTTTTCAATTCAC | 5336 |
| rs149318836 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800725 | GATAGGCAGAATAAA[C/T]GCTCTCTGCTCCCAA | 5336 |
| rs149333892 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857306 | AAACTCTGCTCTGGA[G/T]TTGGACACCTGGGTT | 5336 |
| rs149354408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855530 | TTCATTCTTTTACTA[C/T]ATGTCTTTTGAGCCT | 5336 |
| rs149356390 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815219 | GAGGTTTTATTGCAT[A/G/T]TGGGGCCTTACTGGA | 5336 |
| rs149394028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796350 | TGGACCCCTGAGAGA[C/G]AGGCCTCCTATGGGC | 5336 |
| rs149401729 | snp | C/G/T | 9.99678e-05 | 0.00706934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883357 | GTGAGAGCACAAGGT[C/G/T]TGTGGGTGCCTGAGG | 5336 |
| rs149402904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846424 | CTTGAGCAAGAATTC[C/T]TGACTCAGGCTCAAC | 5336 |
| rs149407635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852539 | CTGGTCATCTTGTAG[C/G]GGGAAGGAGGAGTCA | 5336 |
| rs149416970 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950075 | AGAGTAAAAATAATG[G/T]AAAGAATCAGAATAA | 5336 |
| rs149439306 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823417 | CCTCGCCCCATGAGA[C/G]TCCAGGTGAAGATTG | 5336 |
| rs149454268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945129 | TGTAAGAATGTGACC[C/T]TCCTCTTCATAAGCA | 5336 |
| rs149456103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901816 | CTTATTTAAGATGTT[A/T]ATGAAGAAACCCATC | 5336 |
| rs149471008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936747 | CCAGAGACATTTACA[C/T]GCTGGCATAACTAAC | 5336 |
| rs149478592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782606 | AATTGCATCTCATAA[A/G]CTCATTCATGTTCTT | 5336 |
| rs149484437 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791815 | CGTGATCTGCCCACC[C/G]TGGCCTCCCAAAGTG | 5336 |
| rs149487504 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961863 | ATAGCAATGTGCAAG[A/C]AGATAGAGATTTTCA | 5336 |
| rs149492104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879535 | TTCTCAGAGGCCTGC[A/G]ATTCCCTTTCTAGAA | 5336 |
| rs149493442 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840538 | GACAGTTCTATCTGG[C/G]AGTGATGGGAGACAG | 5336 |
| rs149516701 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816976 | TTTCCTATGCCCATT[A/G]CACAGTTACCCATTT | 5336 |
| rs149524231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932966 | ACAGGGAGGTGCCAC[A/G]ACCCTGAGGTTTATT | 5336 |
| rs149543842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877733 | ACACCATCACTCCTC[A/G]GCATGTAGGCGTCAT | 5336 |
| rs149560359 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869877 | GCAAGGATGGAGACA[A/T]TGGGCACCGATTTTT | 5336 |
| rs149565026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888962 | CAGAGAGCCCAAAAT[A/G]TTTACCTCTGGCTCT | 5336 |
| rs149568326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833867 | GTGTGTCTTGCCTAA[C/T]GATTGCCTTTGGCGA | 5336 |
| rs149572593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930960 | AGTAATTTGTAAAAA[A/G]TATTTATGATGAGTG | 5336 |
| rs149609083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904233 | ACGTTCTTTGACTTA[C/T]GGGATCCCACAGGGG | 5336 |
| rs149611579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867439 | CATTATGGGCACACT[A/G]GGTTGGAGTTTGAGG | 5336 |
| rs149619554 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829986 | CTGTGGACCCATGAA[A/C/T]GGGCAGTGCTGTCTT | 5336 |
| rs149645375 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927621 | TTGTTCCCTCGCCGC[C/G/T]TCTTGTTTAGAGAGC | 5336 |
| rs149647312 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844050 | GGTGTGACGTCGGCT[C/T]ACTACAAGCTCTGCC | 5336 |
| rs149651652 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805976 | CTAGTTGCCACATTC[A/C]TAAAGGTAAAAAGAG | 5336 |
| rs149653795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799820 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC | 5336 |
| rs149667042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856295 | TCCATGAGGTGTTTG[C/T]ACTGTTAGCTTCATT | 5336 |
| rs149671160 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815808 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 5336 |
| rs149678057 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911449 | GATGAAGATGAATCA[A/G]TTTTTTGAGACAAGG | 5336 |
| rs149707247 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797767 | CCACTCGTGGTCCTG[A/G]CACTTAGTGACTGTG | 5336 |
| rs149713189 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884060 | ACCCCCCAGCGAAGA[A/G]GTATTCAGGGCCGGG | 5336 |
| rs149718876 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829227 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 5336 |
| rs149720938 | snp | C/G/T | 0.00943532 | 0.0680349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891635 | GGGCAGCACAGAGCA[C/G/T]GTGAGGGTTGAGGCA | 5336 |
| rs149721991 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853795 | ACTGGAGGCTGTGGC[C/T]CATTAGTAACAGTCC | 5336 |
| rs149725907 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951584 | TTGAAGCTATACAAC[G/T]TTCATATCAAAACTG | 5336 |
| rs149731731 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908238 | TCTCAGGAGTGGGAG[G/T]CAGGCAGAGGAGGGT | 5336 |
| rs149758836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810786 | CAAAGCACTGTATTG[A/T]GTTCTGATAGAAGGA | 5336 |
| rs149771789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849640 | TCCAGGTCTGGTGGC[A/G]GATGCCTGTAATCCC | 5336 |
| rs149789334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880235 | AACAGTGAGACCCCA[G/T]CTCTAAAGAAACCTG | 5336 |
| rs149790816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841632 | GAGAAAATAGACAGT[A/G]AGCCAGAATAGAGGC | 5336 |
| rs149796811 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938061 | GATCTTTCTTTCTTA[C/G]AGTACACTCCGGGGT | 5336 |
| rs149810114 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792866 | GGAGAGAGCCAGACC[A/G]TATCAGCCACTTACT | 5336 |
| rs149839489 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920189 | CAGGGGCTCATAGGC[C/T]ATTGTAAGGCCCTGG | 5336 |
| rs149856415 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943238 | AGACTGGGTAATTTA[C/T]AAAGAAAAGAGGTTT | 5336 |
| rs149864131 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789416 | CTGCCCAGTCTCCCA[A/T]GTAGCTGAGACTACA | 5336 |
| rs149867368 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778302 | TTGAGTCCCGGAGTT[C/T]GAGGATGTGGTGAGC | 5336 |
| rs149880129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834843 | GAGTTTTTATTTGTT[C/G]CTTTGGTCTTTTATG | 5336 |
| rs149884119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801637 | TTATTTTTTAAAAAC[C/G]TATCTCCCATTTTTT | 5336 |
| rs149886290 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931747 | TCCAGGCAGCAGGAT[C/G]AGCAGGCCCAGGTCC | 5336 |
| rs149891518 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889631 | AGAGGCTGGAGTTTC[A/G/T]TTTTTTTATGTTTTT | 5336 |
| rs149918750 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812339 | CAGGCGTGAGCCACC[G/T]CACCCGGCCTGTTGT | 5336 |
| rs149926950 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868327 | CCTGGCCCTTAGTGA[A/C/G]CTTGCCTTGCTCTGA | 5336 |
| rs149931606 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874692 | GGAGTGGGTTCATGC[C/T]TATCAGCAGCCAAAT | 5336 |
| rs149935471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831443 | CTAAGCACTTGGCCA[A/T]GAACTTGGTCTCCTT | 5336 |
| rs149938950 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929784 | GCTCCGATTACCAGA[C/T]GGGAAAATCAAGGTC | 5336 |
| rs149962119 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905260 | ACCTGGAGGGCAGAG[C/G]TGAACAGACTAAGAG | 5336 |
| rs149979907 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882381 | GCAGTTAATTTTGCC[C/G]TGATGGCCTGGAGTC | 5336 |
| rs149982294 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826962 | GTGGATCCGATGAGA[A/T]GACTGAAGATAGGAC | 5336 |
| rs149990947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948375 | TCTTCCATGGGCAAA[C/G]TGGCCATTTCTGGAG | 5336 |
| rs150003022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862165 | CGAGACGAATCGTGT[A/T]TCCTGAAGGAAAACA | 5336 |
| rs150007071 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960376 | ACAGGCACATTCTGA[A/G]AGATGGAAGCAGCAC | 5336 |
| rs150014459 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925781 | AATCCCAGCTACTGG[C/T]GGGGCTGAGGCAGGA | 5336 |
| rs150018426 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808401 | GAGGGTCCTGAGAGA[C/G]TGTACTGGAGAGGCT | 5336 |
| rs150031653 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922975 | CTGCAGGAGTGTAGA[C/T]AGGGGACTGCTGACC | 5336 |
| rs150053878 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897369 | AAAGCACTTACCATC[C/G]TATGCTTCAATTTCC | 5336 |
| rs150054348 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859040 | CTTTTGTGCACATTC[C/T]GTAGGACTCACTTAG | 5336 |
| rs150055545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786501 | CGTCTGGTTCCCACA[A/G]CTGGTCGAGTCATCT | 5336 |
| rs150059912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957780 | ATTGAGGAGATTTAA[C/T]CTCTCTGAGTCTCAA | 5336 |
| rs150083443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850751 | AGCATAGAGAGCTTC[C/T]TCCTGTGTTGCATAT | 5336 |
| rs150101321 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881333 | ACTGAATTAAAATGA[A/G]TTCAGGTGTATAAAC | 5336 |
| rs150106094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842819 | GGGGAGTGAGAGGAA[A/G]CTATGAGACGTACGG | 5336 |
| rs150114568 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947273 | TAGGGAGCCAGGGGC[A/G]TTGTGTGGGGTTCTA | 5336 |
| rs150120418 | in-del | -/CCTAACC | 0.390571 | 0.206736 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923231 | CCCCAAACCCTAACT[-/CCTAACC]CCTAACCCCTAACCC | 5336 |
| rs150121705 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793635 | AAACATATGAGCTGT[C/T]TGTTTCCTTGGTATT | 5336 |
| rs150156555 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878980 | TGTCCGGGCAGGGAG[A/T]TGCAAGACCTGGCAG | 5336 |
| rs150165109 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921884 | TTTTTCAAAAATTTA[C/T]AATCCATGGCCAATG | 5336 |
| rs150184544 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932863 | GAACCATGAGCTTGT[A/G]GCCAGCTGCGCTGTC | 5336 |
| rs150190937 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814820 | AGTTAACCTCTCTGA[A/G]CCTTAGTTTCTTTGT | 5336 |
| rs150197503 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788371 | CTGCAAGCTCCGCCT[C/T]CCGGATTCATGCCAT | 5336 |
| rs150203433 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877634 | GCATTCCTCGGAGTG[C/T]GGACACCGCCTGGCT | 5336 |
| rs150241748 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852399 | GTGAATCAGCTCTAT[C/G]TAAAGCACATGGAAT | 5336 |
| rs150253854 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930669 | GGGAGGATCGCATGA[A/T]CTTGGAAGGTGGAGG | 5336 |
| rs150257809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875363 | GAAACTGAGGTCCAG[A/G]GAGGTTACTTTGCTG | 5336 |
| rs150276286 | snp | C/G/T | 0.0121322 | 0.0769375 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81869274 | TAAAGTGAGCAGTGC[C/G/T]AAGTTCCTTAAAGAT | 5336 |
| rs150279139 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796214 | AGACAGCCTCATCTG[C/T]CCTCTTGGGTTTCTC | 5336 |
| rs150290558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870534 | TCTTCCCTTTTGGGG[A/C]TCAAAGGAGGGTCTT | 5336 |
| rs150295322 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827827 | CAGGCACGGTGGTTC[A/G]TGCCTGTAATCCCAG | 5336 |
| rs150312333 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901715 | GTGTTTTCATATCCC[A/C/G]TTTACAGTTATTGCA | 5336 |
| rs150312478 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863585 | TGAATTGCTGGATCA[G/T]TTGCTGGATTGCTGT | 5336 |
| rs150328572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926340 | AGAGTCCCTGGCTGC[A/G]GAAAATAGCTCAAGA | 5336 |
| rs150331445 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808937 | TGTAGTTTGTGGCCT[A/C]TTGGACCTGCCTGAT | 5336 |
| rs150361813 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840244 | GCCCTGACAGCTGGC[C/G]CCTGAGCTGCCCACC | 5336 |
| rs150365982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898338 | AAGCAGCGTTCATTC[A/G]AATGGTTCAGATTTT | 5336 |
| rs150373107 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942211 | GCCTTGAGCCTCATA[A/T]CCCCTCCCAGTGCCT | 5336 |
| rs150383366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807065 | TCCATTCTACCTTCT[C/T]GCCAAGGCTTCCTAG | 5336 |
| rs150393459 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956054 | ACGCTCATTAGCTGC[A/T]GCCACTCACTCCATC | 5336 |
| rs150400678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800625 | TATTGTTGATGGGCA[C/T]TTGGGTTGATTCCCT | 5336 |
| rs150403033 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816408 | CAGATACTGAACTAT[C/T]TGGCATATCCTATTT | 5336 |
| rs150415193 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857203 | TCTCCGTCATCCCTC[G/T]CTTCTGGTTTAATTA | 5336 |
| rs150418160 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918337 | ACAGTTTCAGGTCTT[A/T]TGTTTAAGTCTTTAA | 5336 |
| rs150451656 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829605 | AGTTCCAGAATTTAT[C/T]TGGACTTTAACAGTT | 5336 |
| rs150454792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798558 | CACAGCCTGGGGGCC[A/T]CTCCACTGTCACAGG | 5336 |
| rs150483905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928361 | CTCCGAACCTCCTGG[C/T]ACCCTCTCCCCGCCA | 5336 |
| rs150486474 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885544 | TTCTTCATTTCTTTG[C/G]TGAAGAATTCTAAAG | 5336 |
| rs150519505 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878311 | TTTTAAGAAGCCAGG[A/C]ACTGGATTCGGGTCC | 5336 |
| rs150521011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837613 | AACCAAGGTTGGGAG[C/T]GTGGTTTCCTTCTCA | 5336 |
| rs150535176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939630 | TCCCCCGTTCCCTTG[C/T]CCCTGATCCTGGGGC | 5336 |
| rs150563831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819739 | ACAGGTACCCACCAC[C/G]ATGCCTGGCTAATTT | 5336 |
| rs150565405 | snp | A/G | 0.000603156 | 0.0173555 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81785982 | CCTTCTCCCTGGAGC[A/G]GCCGACAATGTCCAC | 5336 |
| rs150571424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876228 | CAGTTTCACCATGTT[A/G]CCCAGGCTAGGCTTG | 5336 |
| rs150580037 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797514 | CCACAGACTAAGAGT[A/G]CTGGGAGGCCAGGGA | 5336 |
| rs150594348 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853563 | ACAACCTGGATCCCT[C/G]GCATGCGTAGTTCAC | 5336 |
| rs150605543 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778043 | AAAACAAAAAAAAAA[A/C]AAAAAAAAAAACAAA | 5336 |
| rs150622154 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890962 | GAGGTTAGGAGTTTG[A/T]GACCAGCCTGGCCGA | 5336 |
| rs150639602 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865250 | ACTCTCTGTAGGGGA[C/T]GGCAGGTTGCAGAGA | 5336 |
| rs150640292 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902667 | AGCTCTACCCTCATT[C/T]CCGTTCATGAGGACT | 5336 |
| rs150647112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871412 | GGTGTGATCTTGGTT[C/G]ACTGCAACCTTTGCC | 5336 |
| rs150662770 | in-del | -/CTC | 0.266819 | 0.249434 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893432 | TGCTTTGACCAACTT[-/CTC]CTCAAAAGAACACGT | 5336 |
| rs150681637 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846061 | TGCTGTTGTGCCCCA[C/T]TCAGCTCCCATTACC | 5336 |
| rs150685966 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807517 | AACGCCACCATAAGA[G/T]CTGACATTTATGTAG | 5336 |
| rs150689672 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900481 | CCTTCTGGGAGGGCA[G/T]ATGTGGGGGTTGTGC | 5336 |
| rs150696922 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789844 | CCCTTCCCACCTTTG[-/C]CCCCCCCTCCATTGC | 5336 |
| rs150720490 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805623 | CAGATGCCTCACACC[C/T]CCTTCCCCCACCCCA | 5336 |
| rs150727140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858127 | GGTGTGAAAGGGGAT[A/G]CTTTCTTTGCCTTCT | 5336 |
| rs150738600 | snp | C/T | 0.0364509 | 0.129988 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961522 | CTTTTGGTACAGAGA[C/T]AGAATTAAATAACAT | 5336 |
| rs150745077 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919956 | ACAGAGTGATGGGGA[A/C]GGGGTTGAAGTTTTC | 5336 |
| rs150752562 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781877 | CTTTCCCCCCCCCCC[C/G/T]CCGCCCGCCCCCGAG | 5336 |
| rs150764230 | snp | C/T | 0.084364 | 0.187256 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954549 | CTCCCTGTGTCCTCA[C/T]TGTTCAACTCCCACT | 5336 |
| rs150765969 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831011 | CATTTCCATCTTGGG[G/T]CCTTTGCATTTACTA | 5336 |
| rs150768031 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799381 | TTTCATTTTGTACTA[C/G]TTTGTGACCATGTTA | 5336 |
| rs150769276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782566 | GTGGACTCCAGGGAT[C/G]TTTTGGCCGTGAAGA | 5336 |
| rs150772465 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803949 | GCCTCCCAGAGTGCT[C/G]GGATTACAGGTATGA | 5336 |
| rs150781205 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894183 | CCTGTAATCCCAGCA[C/G]TTCAGGAGGCTGAAG | 5336 |
| rs150782447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855841 | AGGGAAATAGCATGT[C/T]GGATGTAGGAAATGA | 5336 |
| rs150799909 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929539 | TAGCCGGGACTACAG[A/G]CATGGGCCACCGTGC | 5336 |
| rs150819348 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851439 | CACGTGTAGGTGGGT[A/G]TGTCTACCACCGTAC | 5336 |
| rs150833842 | snp | A/G | 0.0121728 | 0.0770598 | missense | PLCG2 | GRCh38.p7 | 16:81912673 | GACGGGGCCTTCCTG[A/G]TCCGGAAGCGAGAGG | 5336 |
| rs150843048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795080 | GCAAATACTCAAAGA[A/G]GACCTGATGTGTGTT | 5336 |
| rs150850754 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882212 | ACTCCCCATCCAACC[A/C/T]GGGGGTGGCTCGTGC | 5336 |
| rs150857242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888939 | GTTGCGACAGACACC[A/G]TATGGCTCAGAGAGC | 5336 |
| rs150862460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948081 | TCGTTGGCAGTTCTT[C/T]ACTTTATAAATAATA | 5336 |
| rs150894666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867390 | ACTTCTCCTTCTTGT[A/G]TGAGCTACTCGCTTG | 5336 |
| rs150896141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824197 | GGAGTGCAATGGCGT[A/G]ATCTCAGCTCACCGC | 5336 |
| rs150903401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879688 | AAGTGCTTATCCAAT[C/T]GCAGTGTCATTGAAG | 5336 |
| rs150903599 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922775 | CGTCAGAGCTTTTCC[C/T]ACTAACATTTGCTTG | 5336 |
| rs150906807 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945795 | GTGCTTTGTAAGGCT[A/G]TAAGTGGAGGAAATG | 5336 |
| rs150923293 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934365 | GGAGGAGGAAAAATG[C/T]AGGGCGAGCTGGGAA | 5336 |
| rs150926283 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815799 | GACACAGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 5336 |
| rs150947179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811155 | CAGTGTTGGGGTTGA[A/G]CAAGCCTGGGCTTGC | 5336 |
| rs150956606 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850617 | CACAAGAGAAAGAGA[A/T]TTCTCTTCCTGGCTC | 5336 |
| rs150959738 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872473 | AGATAGGCAGGAAGG[A/T]TAGTTACCTTTTCTT | 5336 |
| rs150959987 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911300 | TGCTATTTCTTATCT[G/T]AAGAAATAACCCGAA | 5336 |
| rs150967878 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927771 | TTTAAGGGTCAAATA[A/G]TCCTTCCTCCAGGAA | 5336 |
| rs150998471 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847842 | TATGCAAATTCTCTG[A/C]CATTTTTTATCAGAG | 5336 |
| rs151005698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944524 | CTGAAATTCAGTGTT[A/G]TGTGATCATAGCTCA | 5336 |
| rs151013036 | snp | C/G | 0.000615431 | 0.017531 | missense | PLCG2 | GRCh38.p7 | 16:81907750 | TGATGACATTGAACA[C/G]ACTATGGAGGAGGAA | 5336 |
| rs151029652 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898049 | GCAGATGGAAGGAGC[C/T]GGTATTAACAGACAC | 5336 |
| rs151047143 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806815 | TTGAGGGCTTCAGGA[A/G]TGGCCAGGACAAAGC | 5336 |
| rs151080308 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895130 | CCACATGACCCATTT[C/G]TGTTTGAAAATATTA | 5336 |
| rs151085235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784056 | ATGCTTCTGCTGCTG[C/G]ACTTGTAACTACATT | 5336 |
| rs151094135 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962367 | GAATTATACAGAATT[A/T]GAAAATTGGCATTTA | 5336 |
| rs151098660 | snp | A/C | 0.198014 | 0.244535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841486 | CCTCAAGTGATCTGC[A/C]CACTTCGGCCTCCCA | 5336 |
| rs151102916 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804929 | AGCTCACATGTATCC[A/G]TGTGATCATGTGTAT | 5336 |
| rs151119357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875183 | TGGCCAGGCTAGTCT[C/T]GAACTCCTGACCTCA | 5336 |
| rs151120062 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832076 | GGCTTTGTCGTCCTC[C/T]GGCCTCAGTCTTCTC | 5336 |
| rs151133454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914291 | GGTCAGGATGCCACC[C/T]GTATGTGCATGCTGG | 5336 |
| rs151138793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801555 | TTTAGGTTGTTTCCA[A/G]TCATGATACTCCCGA | 5336 |
| rs151157588 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827415 | GCTGATCTCGAACTC[C/G]TAGGCTCAAGGAGTT | 5336 |
| rs151158996 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795803 | CTCCTCGGATCAAGT[A/G]ATCCTCCTGCTTTGG | 5336 |
| rs151165153 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926214 | GGAGGTGATGTCTGG[A/G]AGTCCTGGGGTCAGA | 5336 |
| rs151169453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889536 | GCAGGGGAATTGCAA[C/T]AGGGAAAGAGCTTAA | 5336 |
| rs151173884 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851896 | AAGCTTTGAGTGCAT[A/C/G]CCATCCCCTCTCCTC | 5336 |
| rs151180912 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949515 | ATTCAGTGTCCAGCC[C/T]CCGACATGTCAAGGA | 5336 |
| rs151209356 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824834 | ACATTATGTGGCAAA[A/G]GAGATTTTTGCATGT | 5336 |
| rs151222919 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886896 | ATTTTCACTATTACA[A/G]GTATCTAGTGCAATA | 5336 |
| rs151240767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878899 | CTGCGTCCCAGGGGC[C/T]AATTCCTGCAAACAC | 5336 |
| rs151258909 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824036 | TTCCTTTCCTTTCCT[G/T]TCCTTTCCTTTCCTG | 5336 |
| rs151261127 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791262 | CATTTGGATGTGGGG[C/G]AGGTGGTGAGGAATG | 5336 |
| rs151270814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941369 | GCAGGTTCCTGGACC[C/T]ACCACAGGGTGATGA | 5336 |
| rs151293388 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917911 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 5336 |
| rs151310079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821271 | AATAATGCCTGGCAC[A/C]TAGCAGATGCTAAAT | 5336 |
| rs151332255 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813882 | TGAAGCTTTTGCTGT[A/G]TTAAAAGGAAGTCAC | 5336 |
| rs180674297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806718 | AGGTGTGGGGCTGGG[A/G]ACATGGAAGGCCTCA | 5336 |
| rs180681486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817278 | GCATCCATCCCCCAT[A/G]TATAAAATGGGAATA | 5336 |
| rs180682402 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802407 | GTGAGCCACCGCGCC[C/T]GGCCTCAGGTGGGTA | 5336 |
| rs180683138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791418 | GTGGGTCATAGATCT[C/G]GGCAGAGCTCAGCTG | 5336 |
| rs180689293 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828021 | CTTGCACCTGGGAGG[A/C/T]GGAGCTTGCACTGAG | 5336 |
| rs180691563 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812285 | TGATCTCCTGACCTC[A/G]TGATCCACACGCCTC | 5336 |
| rs180698637 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823903 | TTCTTTCCTCCCTTC[C/G]TTCCTTTCCTTCCAT | 5336 |
| rs180774689 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959143 | GGTGGTTGGTAGAGT[A/C]ACAACTTCTCAATGA | 5336 |
| rs180779653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947837 | GATGTAAGAAAGGTG[A/G]GGGAGTTGAAAAGAG | 5336 |
| rs180785035 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954126 | CTCCTGGGCTCATGT[C/G]ATCTTACCCTCTCAG | 5336 |
| rs180804473 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938486 | GGGTGTGGAAATCCA[C/G]TGATTAAGCTCTGCC | 5336 |
| rs180812584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914292 | GTCAGGATGCCACCT[A/G]TATGTGCATGCTGGC | 5336 |
| rs180813573 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933129 | AAGCTGAGCTGTTCA[A/C]GGTTGCTGTTGGCGG | 5336 |
| rs180816468 | snp | C/T | 0.000881501 | 0.0209755 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908614 | CCCCGACCCAGGGAA[C/T]GCCTACCTTCTTCTC | 5336 |
| rs180818434 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926683 | ACAGAAAGCCTCCAC[A/C/T]GTCAGTGGTAGAGCT | 5336 |
| rs180819449 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901406 | ACAGAAGAGTTTATT[C/T]CTTCCCCATGCGAGG | 5336 |
| rs180829419 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883648 | GGGCCTGAGGATGGG[A/G]CTGCCCTCACCTGGC | 5336 |
| rs180831354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878335 | CGGGTCCACCCTAAC[A/C]CAGCAAGGCCTCATC | 5336 |
| rs180832304 | snp | A/C/G | 7.29439e-05 | 0.00603882 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921154 | TGTAAGGGCTATTCC[A/C/G]GGAGCATGGATTATT | 5336 |
| rs180833586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888138 | CAATAAATGACTTGC[A/G]GAGTTGTGTGGACTA | 5336 |
| rs180837513 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943612 | CATTAGAGATGCAGA[A/G]TCTCAGGCCTCACCC | 5336 |
| rs180866587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895366 | GAGATTGAGACCACC[C/T]TGGCCAACATGGTGC | 5336 |
| rs180870043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865629 | TGGTTCCTTTGCCCT[C/G]CTGCTGTCTGGGCTC | 5336 |
| rs180914542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782583 | TTTGGCCGTGAAGAT[C/G]TGTTTCCAATTGCAT | 5336 |
| rs180917139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814279 | TAAGGTCTTCTCAGG[A/G]GACCTGCCTGTTTTA | 5336 |
| rs180920277 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788608 | CCTGTTGCCTGAACC[C/G]TCATCTATGCTGCGT | 5336 |
| rs180925283 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800016 | GCTATGCCACTTATC[A/C/G]CATTTGTGGCCATGG | 5336 |
| rs180925325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825934 | AGAAGACATAGAAAT[A/C]AGATGGCATTGGACC | 5336 |
| rs180929720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809872 | AAGCAAAAAAAGAGA[A/G]TTTACTGGAACGTGT | 5336 |
| rs180930348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804253 | ACCATCCTAGTGGAG[C/G]TGAAGTGTTATGTCA | 5336 |
| rs180965748 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793309 | TCTTTCCTTTCTGAG[G/T]GACCTAGTTGAGCAG | 5336 |
| rs180968115 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821123 | TCTAGAACTCCTGAT[A/G]TCAAATGATCTGCCC | 5336 |
| rs181017673 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945556 | ACCTTTGAGATGTGT[G/T]GCCTTAAACATTACT | 5336 |
| rs181028180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950399 | CATTAGCAAATAGCA[C/T]AGTACCTAAGTATAT | 5336 |
| rs181033879 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936055 | CCCTTGAATGTCAAA[C/G]AGGGAGATTCCTGGT | 5336 |
| rs181041643 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961970 | TGTCACCCCATTGAT[C/T]GCCAGGGTTGATTCG | 5336 |
| rs181043336 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924420 | TGAAATAACTCACTT[C/G]ATTTGAAATAACTGA | 5336 |
| rs181047597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957288 | TGGGCACCAGAGGGA[C/G]ACTCTGTCAAACAAA | 5336 |
| rs181052764 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911482 | TTGCTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 5336 |
| rs181056909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885301 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACCACG | 5336 |
| rs181067881 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877095 | TGTCACCGTCTTGCC[C/G]CAGCTCATGGAGCCC | 5336 |
| rs181110012 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778711 | GCCTAAGGTAGCAGT[A/C]AGGGTTGGTCTGACT | 5336 |
| rs181115602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929370 | CTGCTTCTATTGCCA[A/G]TGCTCTGCTTTACAC | 5336 |
| rs181129641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904329 | TGGCCAGTAAGGTAA[C/T]AGGCCCTGAATTCAA | 5336 |
| rs181133031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791189 | TTGCAAGATTGTGTG[A/C]TTAGTACCATAGCAG | 5336 |
| rs181137456 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802350 | ATCTCCTGACCTCGT[A/G]ATCCACCCGCCTCGG | 5336 |
| rs181140433 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891667 | GGGTCCGATACGCCG[C/G]TCCGGTGAGCCCTGT | 5336 |
| rs181143662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862311 | CATTTTTTGACTTTT[A/C]TAGAGGCAAATGGTA | 5336 |
| rs181151261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880133 | GTAGTCCTAGTTACG[C/T]AGGAAGCTAATACAG | 5336 |
| rs181155522 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823244 | CCGGGGCTTTACCTC[A/G]AGACTGGATCTCTGC | 5336 |
| rs181157570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854815 | AGAATAATAATGCCT[A/G]TTTCATGGGGGTATT | 5336 |
| rs181167432 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843438 | TTGGATTGCAATATA[A/T]TACATCATATTACAC | 5336 |
| rs181169735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868879 | CCAGTGTAGGTGCCT[C/T]CTCATTGGGGCATCA | 5336 |
| rs181237191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796814 | GCCTCGCCAACACTT[C/T]GATTTTGGACTTCTG | 5336 |
| rs181239717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786531 | TTTCCTCTTAAGGGC[A/G]AATTAGCCCAAGCCT | 5336 |
| rs181242905 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947943 | ATATTTCCATAGTCA[C/G]ATTCATACAGGTGCC | 5336 |
| rs181250983 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818099 | ATCTGTGAAGTGAGA[A/G]TTACAACACCTACTT | 5336 |
| rs181254434 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959495 | TCAATCATCTCCATC[C/T]ACAAGCTCCTAAAAG | 5336 |
| rs181286423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808031 | ACATGAGACTGCTGC[A/G]GAGACAGATATGCAA | 5336 |
| rs181317125 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828769 | ATTGAACAATGTGGC[A/G]TTTTCCTGAGTGCCT | 5336 |
| rs181344954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943122 | TACCTGATAGCCTCC[C/T]GGAATGCCATGGAGC | 5336 |
| rs181346398 | snp | G/T | 0.000332 | 0.0128798 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927048 | ATTCATGCCACCTGG[G/T]GACAGCGCCCCCATG | 5336 |
| rs181348539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932533 | AAAGCCTTCCTGGGG[C/T]CTCTTGTGCCCTCTG | 5336 |
| rs181359761 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920320 | AGATTTATGGCATCC[A/C]GATCATGTGCCAAGG | 5336 |
| rs181366246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901941 | AGGGTCTGTAGCTTT[C/T]CCCAGATTTTGAAGG | 5336 |
| rs181376816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907176 | CGTTATTAAAAAAAA[A/G]AGTTTCTGCATACCC | 5336 |
| rs181381635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894485 | GGGCAGATGGCAGAC[A/G]CCTTATTTCCCTCCT | 5336 |
| rs181382731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882936 | CTTGCTACACTGTAT[C/G]CCATATGCCTGGTTC | 5336 |
| rs181385599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873452 | AGAATAATGATGACA[A/G]TGTGCGTATGAAATT | 5336 |
| rs181389877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840221 | CTGGAGAGCATGCTT[A/C]GAATTGAGCCCTGAC | 5336 |
| rs181392668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857974 | AACAATGTCATAGTG[A/T]TAGTTCCCACCACTC | 5336 |
| rs181398038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878652 | CTCCTAGAGCACTTC[A/G]TCTTGGCACGTCAGC | 5336 |
| rs181414365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851581 | GCAGTGGCGTGGTCT[C/T]GGCTCCCTGCAACCT | 5336 |
| rs181438531 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81831084 | TGTCACCACCTCTGG[A/G]GAGGCCTCCCTGATA | 5336 |
| rs181465880 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81788179 | CCATTTATATTCCTT[C/G]CAGTGGTAGAAAAGG | 5336 |
| rs181466570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814990 | ATAAGAAGTTACTTT[C/T]ATTATTATCAGGACT | 5336 |
| rs181475723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826648 | AGCAGCCACTCATTA[A/C]CCACGTCCTCTCAGT | 5336 |
| rs181477368 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938728 | GTGTCACTCTAGAAC[A/C/T]CAGCTGCAATCCACG | 5336 |
| rs181482518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809631 | TGTGTCAGGAAACAC[A/G]TGGACCAGACTTGGG | 5336 |
| rs181487860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914458 | CTTCAATGGGACCGC[G/T]TGAATGAAGAGGTTG | 5336 |
| rs181487940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953075 | CGCCTCAAACAAATT[A/T]TAAGAAGACACCAGA | 5336 |
| rs181500486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888572 | ATGCTTCATACAGTG[C/T]ACATTTCATACAATG | 5336 |
| rs181553874 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918059 | TCATTTATTTTCTTA[C/G]TATTGAGCTGTTTGA | 5336 |
| rs181574733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904573 | CCCCATTGGGTCCCC[C/T]GCCACCCTGCCCAGC | 5336 |
| rs181586385 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880295 | ACCCCAGTGGAGGTG[C/T]CTATCTCAACTGTTT | 5336 |
| rs181588253 | snp | C/G | 0.000399281 | 0.0141238 | missense | PLCG2 | GRCh38.p7 | 16:81923506 | AGAACCGTGAAAGCT[C/G]TGTATGACTACAAAG | 5336 |
| rs181588282 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891715 | GTGTAGCACCGCATT[A/C]CTTGGACTAAAATAC | 5336 |
| rs181599034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870181 | GAAGCATTTACCATT[G/T]ATTGCTACACAGTTG | 5336 |
| rs181602941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798855 | TCAGGGATCCCACTG[C/T]GTCTTCTCTGCTCCT | 5336 |
| rs181603471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855283 | ATTGATCTGAAGGAA[C/T]TGTCCTGAGATCTTC | 5336 |
| rs181609140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843691 | TTAGGATATTCTTCT[A/G]TCCTCCAACTACCTT | 5336 |
| rs181619136 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820720 | CCGCCTCCCAGGTTC[A/G]AGCAATCCTCCCACC | 5336 |
| rs181655438 | snp | C/T | 0.016764 | 0.0900053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786207 | CGCTGGGTGGGGCAG[C/T]GTGGCCCGTCCTCTG | 5336 |
| rs181656912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796485 | CTGTAAGAGGACATC[A/G]TCTGGCTCCCGGGCT | 5336 |
| rs181663081 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807216 | CATGTCTTGTCCCAG[C/T]GGTGTCCTCCTCCTA | 5336 |
| rs181669936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817456 | ACGCTGGAGTGCATC[A/G]TCTTGAGGGGTGCTG | 5336 |
| rs181683870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950432 | GACAAAAATTCCTAC[A/G]TATACAAAGACAACT | 5336 |
| rs181693005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929572 | GGCTAATTTTTGTAT[G/T]TTTAGTAGAGCTAGG | 5336 |
| rs181708369 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911065 | TGAAAATGAACAAGG[A/G]AACAATGATTATAAG | 5336 |
| rs181725138 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884513 | GACAGGTGGTTTACC[C/G]TTTTTGTGCCCCAGT | 5336 |
| rs181742206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860779 | AGTTCGAGACCAGCC[A/T]GGGCAACACGGTAAA | 5336 |
| rs181751301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835974 | TCCAGCATGAGCTCA[C/T]CTTGACTACATCTGC | 5336 |
| rs181761884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940606 | AGATCCCTTCATGGT[A/G]TAAGAAGGGTCATTT | 5336 |
| rs181762692 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778328 | TGAGCTATGATGGCA[A/C]CACTGCACTCCAGCC | 5336 |
| rs181774070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953361 | GCGAGATGTTAACAC[A/T]GTGGAGTCTAGGTGG | 5336 |
| rs181774773 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962157 | GGAACCTCCAAACAA[C/G]CTCTCAAGATTGCTG | 5336 |
| rs181774922 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887590 | TTTTGTCTTGCACCC[A/G]TGCATGTCACCAGCC | 5336 |
| rs181777363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932656 | GGCCAGTCCCTGGTC[A/T]CGAGAGGATCCTTGA | 5336 |
| rs181781773 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943281 | GTTCTGCAGGCTGTA[A/C]AGGCTTTTGTTTCTG | 5336 |
| rs181784439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878127 | GCTGGGGACTACAGG[C/T]GCCCACCACCACGCC | 5336 |
| rs181794952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865423 | GGTGAGGCTGTCCCA[C/G]AGCTAGGAGCCCAAA | 5336 |
| rs181795415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920663 | GGTGACATGAGGAAC[A/C]GAAAGAAGAGTTAGA | 5336 |
| rs181797983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851317 | GTCGCTGGTGCAGTG[C/T]TATTAATGAAACTGC | 5336 |
| rs181805743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839371 | AAAAAAAAAATCTCT[A/G]TATAGTCTTTGTATA | 5336 |
| rs181861364 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787932 | GCAGAATCACGATAC[A/C/G]TTGTATGGGTATTCC | 5336 |
| rs181867025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798537 | GAAACAGTGATGATA[A/C]CACATCACAGCCTGG | 5336 |
| rs181870215 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783296 | TTTCAGCTACTTTTT[A/T]AAAATTTTATTATTA | 5336 |
| rs181876143 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809183 | TTGGCCTGACCTTAT[A/C]CCCTCAGCACACACC | 5336 |
| rs181880865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897602 | CCAGGCTAGAGTGCA[A/T]TGGCAGGATCTCGGC | 5336 |
| rs181910984 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960233 | GACTGATTCTCTCAG[A/G]AAAGGCACACATGGT | 5336 |
| rs181929328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875887 | GAAGTGAGTGATGAG[C/T]GTTCTGTGACGATGT | 5336 |
| rs181947087 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962811 | AGTTATTTTTTGAAA[C/T]GTGTTTTACTATCCT | 5336 |
| rs181949687 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894854 | CGCCAGCCTGGGCAA[C/T]AGAGGGAGACTTTGT | 5336 |
| rs181960973 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941620 | AACATTGCTACTCTA[C/G]CAATAATAATGAGTA | 5336 |
| rs181970455 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873970 | TAAATTGGAATCAGA[A/G]TTTTACAAAATGTCA | 5336 |
| rs181970768 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929923 | GCAGAGCAGAGGCAC[A/C]TGGCTCATTGGTTCT | 5336 |
| rs181973961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950615 | AATTTGATTGCATTC[A/G]TTAGAAAACTTTAAT | 5336 |
| rs181978879 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884990 | CCTCCTGGGCTCAAC[C/G]GATCCTCCTGCCTCA | 5336 |
| rs181981317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845914 | AAATGCTGGCTCTTG[C/T]ACTTGTGGCTGGTGA | 5336 |
| rs181989700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876071 | CACTTTGTCACCGAG[A/G]CTGGGGTGCAGTGGT | 5336 |
| rs181993513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861799 | ATCTGGCTCTGAAGT[C/G]GGCTCTTCGTTTGTG | 5336 |
| rs181996490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848140 | AAGAATAGAAAGATT[A/G]GTAGAACAGGATCAA | 5336 |
| rs181999064 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847789 | GTATTAAAAGTAATC[A/T]AGGGATTTAAGGTAT | 5336 |
| rs182037993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793505 | TTGAGGGCCTGGATG[C/T]GTCCATCTCAACTGT | 5336 |
| rs182058198 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814756 | ATGGAGAGCAAGGAC[C/G]CAAGGCTTTTGTCCT | 5336 |
| rs182059362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786922 | TCCTACTGAGGCAAG[C/T]TCATTACCAGTTACT | 5336 |
| rs182071302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796849 | CCAGAACTGTGAGAC[A/T]AACTTCTGTTGTTTC | 5336 |
| rs182080456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785886 | GAAGTTCATGCCCTG[A/T]TAACTAAACCCCTTT | 5336 |
| rs182164004 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960608 | GTAGAGGGTCTTGTT[C/T]TCCAAATTCGATCTC | 5336 |
| rs182192525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927618 | TGGTTGTTCCCTCGC[C/T]GCCTCTTGTTTAGAG | 5336 |
| rs182194581 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874413 | TTAAAAATTTAATTT[A/C]GTGACAGATTTGAAT | 5336 |
| rs182195298 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949079 | TAGTGACACCAAAGA[A/T]AATGTGAAGGAAAAG | 5336 |
| rs182197892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939247 | GAGACACAGAGAGAG[C/G]GGGTGAACCTACGTG | 5336 |
| rs182199527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858816 | TATTTTCCTTCCACT[A/C]AATCAAAGTCCTCTA | 5336 |
| rs182206775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846181 | AAATCTGCATCACCT[A/G]GGAGGTTGTAGTGGC | 5336 |
| rs182211616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831968 | CTCCTCTTGCCCTAG[C/T]GGAAGGGACTGACTT | 5336 |
| rs182212263 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945088 | GTGTAAAAGGAGAAA[A/C/T]TGGGGAGAGAAAAGG | 5336 |
| rs182213673 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924024 | CAGGCGCTTTCCAAT[A/G]CACAAGACTGTGTGT | 5336 |
| rs182232729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915929 | TGGTCCTTCTAATCT[C/T]AGTAGAGAGGTCCTG | 5336 |
| rs182236081 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898477 | GGGTCCACGCTTCCC[A/C]GGAGTGATGAGGCTA | 5336 |
| rs182239049 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883053 | CACCAGGGCCTGCCC[C/G]TTGAGATTCCGATGT | 5336 |
| rs182250799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902660 | TCATAAAAGCTCTAC[C/T]CTCATTCCCGTTCAT | 5336 |
| rs182258844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890189 | GAGGAAGTTGCTAAT[C/G]TTGTAACCTCCAGAA | 5336 |
| rs182262269 | snp | A/G | 4.96866e-05 | 0.00498406 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858232 | TTCCCAGGAATTAAC[A/G]CAGCATTTCTGTTCC | 5336 |
| rs182276717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831307 | AACAGTGCCTGGCAC[A/G]CTGGCTTTTACCTAC | 5336 |
| rs182302812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854312 | GACACTGAGTCCAGA[C/T]GCAGAGATAGCTTTG | 5336 |
| rs182329329 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804770 | GCTCCTCTGCCTCCT[C/G]TTTGGCAATCAGTTA | 5336 |
| rs182362574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826363 | CTCACCTAGGTGCAG[C/T]AGGAGGTCAGTGTAG | 5336 |
| rs182388156 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808266 | GGCTACACTGTTTTG[C/G]ATTTGCCAAGGCCTG | 5336 |
| rs182390751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871206 | TTTGATTGGAATTTG[A/T]TCTGAGTCTGTTAAA | 5336 |
| rs182399338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856078 | CTTGGTCCCTCTTCC[A/G]GAACCCTAAATTCAA | 5336 |
| rs182400244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792141 | CCAATTTATGATGCA[A/C]ATCCCTGCTCTGCCA | 5336 |
| rs182406493 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844244 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 5336 |
| rs182407714 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801379 | TTTGCAGGTCTTTAC[A/G]TAAAAGACACTGCGT | 5336 |
| rs182410245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826837 | ACTCTCAAGGCTGCC[A/G]GAGACAATTTTGAGT | 5336 |
| rs182416809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811217 | CCCTCCTTGGGTCTC[A/G]GTGTCTGCATCTGTC | 5336 |
| rs182422956 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822681 | AGAATCGCTTGAACC[C/G]GGGAGGTGAAGGTTG | 5336 |
| rs182423779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829191 | TCGGCTCACTGCAAC[C/T]TCTGTCTTCCGGGTT | 5336 |
| rs182435132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813426 | GTATTTTATTCTCTT[A/G]GTAGCAATTGTGAAT | 5336 |
| rs182446118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956355 | GCTGCTTAGACACTT[C/T]TGCAGTCAGGTAAAG | 5336 |
| rs182453032 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958328 | GCACGACCTGTGCAG[A/T]GAACAGGATTTCTTT | 5336 |
| rs182459862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937123 | GAAAACCACTGAAGA[C/T]GTGCCTGAGCTAAGC | 5336 |
| rs182463887 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955757 | AAGTCCCACGGATGC[A/G]TCTAGTTGGCCTTGC | 5336 |
| rs182464925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946105 | TATGATCCCGAGGTA[A/G]CCTCCAAAAAAAATC | 5336 |
| rs182469761 | snp | C/T | 3.88901e-05 | 0.00440948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912560 | TGACAGCCTGGAGAC[C/T]GCTCACCTGGTCGTT | 5336 |
| rs182477122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925869 | CCAGCCTGGGGGACA[C/G]AGTGAGACTCTGTCT | 5336 |
| rs182485826 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935911 | GGATGGTGATAGTTT[A/T]AAAAAAAAAGTAAAT | 5336 |
| rs182496189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911196 | AGAAAGCTGCAAAAA[C/T]GTCCATTTCCGAGGA | 5336 |
| rs182539233 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867673 | CTCCTTTTGCCTGGG[A/T]CGTGTTCTCCCTTGC | 5336 |
| rs182557800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841533 | GGCATGAACCACTGC[A/G]CCCGGCTGTAAACTT | 5336 |
| rs182572194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842820 | GGGAGTGAGAGGAAG[C/T]TATGAGACGTACGGA | 5336 |
| rs182573549 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933747 | AGTCACCATTATTAT[C/G]TAAATATTCTCTCAA | 5336 |
| rs182583319 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943826 | AGCAGTATATTCAAT[A/G]AGAGCAATGTCCCCA | 5336 |
| rs182585583 | snp | A/C | 0.000277431 | 0.0117745 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921432 | GATGATTGATAATAT[A/C]AAGCCTAGTTTCAGG | 5336 |
| rs182590830 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796208 | TCTCTTAGACAGCCT[C/T]ATCTGCCCTCTTGGG | 5336 |
| rs182596049 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779821 | GAGCTCGCGGACGCT[C/T]GGAGCCACACTTCCC | 5336 |
| rs182602507 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896088 | CATCAAGTTCTCACC[C/T]GAGTGTTGGCACCCC | 5336 |
| rs182602580 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908918 | CTCACTCACTTTCCC[C/T]GATCCCAGCCCTGGA | 5336 |
| rs182620090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883943 | GGCAGTGTCCAGAGA[C/T]GACATGGGTGCGTGT | 5336 |
| rs182621687 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874715 | AGCCAAATGGTTTCC[A/G]TCGTGAGCTTGCTAG | 5336 |
| rs182631387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781075 | CACTTCTTAATTTAG[A/G]AAACAGCAAGAACAC | 5336 |
| rs182634996 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859350 | TCCTGGAGGGAGCCT[C/G]TATTCCGCAGAAAAT | 5336 |
| rs182650412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791851 | ATTACAGGCATGAAC[C/T]ACTGCACCCAGCCTT | 5336 |
| rs182652808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781662 | AATGCTGCAGGGTGG[G/T]TGTAAGGTGCAGCAG | 5336 |
| rs182657638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818571 | GAGCTTCAGGAATTA[C/T]CTGCTTGGTGGGGGC | 5336 |
| rs182661040 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784414 | ATTTTACAGATGAGG[A/G]AACCGAGCCACAGAT | 5336 |
| rs182661752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803264 | GCTGGGACTACAGGT[A/G]CCCACCACCACGCCT | 5336 |
| rs182664623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803029 | TTACTTTCCCCCATC[A/C]CTGGCAATGACAAAT | 5336 |
| rs182668421 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813353 | TTATTTCCTTGAGCA[C/G]TTGTTTGTAGTTCTC | 5336 |
| rs182673557 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824438 | TGCACATGGCCCCAG[C/G]CACTTATTTTCTTGT | 5336 |
| rs182680859 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961025 | CAAAATGTGGATATT[C/T]GGAAAGTGAAAGACT | 5336 |
| rs182680945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805252 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 5336 |
| rs182694271 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944501 | AGGTCTTCCCTCTGT[A/C]ACTGAGGCTGAAATT | 5336 |
| rs182768826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941923 | GAACCACTGTGCCTG[C/G]CCTATAAACTACTTT | 5336 |
| rs182785681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919366 | GGACTATACCCTGTT[A/T]ATTTACCCACTTCTC | 5336 |
| rs182795575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879044 | AGCATCTGTACCATG[G/T]TGGTACCTCTGCCAT | 5336 |
| rs182796672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892266 | ACCGTGAGAGCTGTC[A/G]GGGAGACCCTGACGA | 5336 |
| rs182803465 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945680 | GTAAAGAGGGAATGG[C/T]TTTAGGAGGAGGAAG | 5336 |
| rs182815047 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919417 | GTATCTAATCAGTAG[G/T]GTTTGTGTAAAAATT | 5336 |
| rs182821948 | snp | G/T | 0.00310765 | 0.0392959 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930639 | TGTGGTCTCAGCTAC[G/T]AGGGAGGCTGAGGTG | 5336 |
| rs182822170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957526 | AGTCCAGCGGCTCTA[A/G]ACTGGGTCAAGATCC | 5336 |
| rs182830121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852776 | TGGGGACTGGGAGAG[C/G]TTGTCTGTGTTCCAC | 5336 |
| rs182831307 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936592 | GGCTTACGCAGGCTT[C/T]GTGATTGTAAGTAAG | 5336 |
| rs182831332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905727 | GTAGTGGTGTGATTG[C/T]GGCTCACTGCAGCCT | 5336 |
| rs182839741 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893432 | TGCTTTGACCAACTT[A/C]TCCTCAAAAGAACAC | 5336 |
| rs182842398 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81881875 | CAGTCTGGTGTTGAA[C/T]TCATGACCTCAGGTG | 5336 |
| rs182854919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871293 | CTGTTATTATTAATA[A/G]CCATCTCCAGATTGA | 5336 |
| rs182857110 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857164 | TATACTTTGGCACCA[G/T]GCAGGTGTTTCCACC | 5336 |
| rs182873499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793760 | GGCACATCAAAGATA[A/T]CTCCTTAATCCCCGC | 5336 |
| rs182874777 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805137 | CAAGACAAGCCACAG[A/T]TAGGGGAAAATATTT | 5336 |
| rs182945645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794460 | AGAAATAAGACGCAA[C/G]CAATGCCTGAAGTGT | 5336 |
| rs182965878 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815717 | GCTTCTTCGATTCTC[A/G/T]CGGTCTTCTTGGTGG | 5336 |
| rs182978418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797129 | AGTGGGTAAACGAGG[C/G]AGGCAGCATTTGTCC | 5336 |
| rs182990027 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808643 | GGACTACAGGTGCCC[A/G]CCACCACGCCTGGCT | 5336 |
| rs182995104 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818984 | ATTTCCAACACTGTC[A/C]TCTTATTTCATCCTT | 5336 |
| rs183003947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829373 | CTCGGCCTCCCAAAG[A/T]GCTGGGATTACAGGC | 5336 |
| rs183010522 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950845 | ACAAAGAATGAAGAC[A/G]TATGTACTACTAAGT | 5336 |
| rs183015266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955264 | GGAAAAAACCTTGCA[A/G]AGTATGGTCTGAGTC | 5336 |
| rs183025017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944203 | TTGAATTGTATACAT[A/C]AATAAGATGGATTGA | 5336 |
| rs183037721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837890 | TCACAACATTCATAG[A/C]ACCCACTACCAGTCT | 5336 |
| rs183042644 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930315 | TTCTCTGTAAGATCC[G/T]TTCTCTGTGTCTGGA | 5336 |
| rs183045528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934222 | TGCACACCAAAACCT[C/T]GTGGAAACAGCTTTG | 5336 |
| rs183046229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949237 | TATTAATGAAATAGC[A/G]AATAAAGGAAGTGTT | 5336 |
| rs183048029 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928058 | GGATATTCTTCATCT[C/G]AGCCAGACCCTGGGA | 5336 |
| rs183065837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905335 | GAAGAGGCAGATGAA[A/G]GCTGCTGGCTCAAAG | 5336 |
| rs183081515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879355 | TTTAAAAAGAAATAC[C/G]TATGCTGTAAATTAC | 5336 |
| rs183132837 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833201 | TTGGGGTTCAGCAAC[C/T]CCAGAATGAAAATCA | 5336 |
| rs183150737 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837232 | TGTGATCAAATGAAA[A/G]GCTGTTGTTGAAAGG | 5336 |
| rs183207603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800541 | CCCTGCGAAGGACAC[A/G]ATCTCGTTCCGTTTT | 5336 |
| rs183213496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784777 | GGACTGGAAATGAGC[C/G]CAGAGGATCTAAGTG | 5336 |
| rs183214349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809957 | TGCTCTCTTCATCTT[C/T]CTGCCAGTCTTTGTC | 5336 |
| rs183214507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794948 | ATTCTTGATGGTGCT[A/G]TAGCCCTTCTCTTAT | 5336 |
| rs183221860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821980 | CAAATTCCTTAACTT[C/T]GCTGAGCCTTCTCTT | 5336 |
| rs183222390 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902312 | TCACAAAATACCCTA[A/C]GCTGGGTGGGTTATA | 5336 |
| rs183226216 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914775 | TGTAACATTGGCTGG[A/G]ATGTAGTTGGTGGTT | 5336 |
| rs183248088 | snp | A/G | 0.00044503 | 0.0149103 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889285 | TGAGGTGAGTAGGCT[A/G]GGCTTGTTGTCGCTT | 5336 |
| rs183253129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867567 | TCAAACAGGTGAATG[G/T]GCATATAAGGCACCA | 5336 |
| rs183254170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789706 | ATTATTATAATAAGT[C/T]CCCCGGATGGTCTGG | 5336 |
| rs183263890 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852193 | GCCACTCCCAGGCTC[A/G]TGTTTTACCAGCTTG | 5336 |
| rs183267778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841177 | ATAAGGGCAGGCCCA[C/T]CCCCTATCTGCAGGC | 5336 |
| rs183290431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829547 | ATATTGCCATGATAC[C/T]TTTGCCAAAAGTGAG | 5336 |
| rs183290593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810307 | CTCTCCTATCCCAGA[C/T]GACTCTAGTCTATAG | 5336 |
| rs183297768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939702 | ACCAGCCTGCAACAG[C/T]AGCTTCCAGGATTGC | 5336 |
| rs183299381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954829 | CTTTATAGTAGAATG[A/G]TTTATATTCCTTTGG | 5336 |
| rs183316385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951891 | GTGATCTCTATTGTA[C/T]ACAAATTTAAACTGT | 5336 |
| rs183320588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916532 | TTGAAATATGTATAC[A/G]TGGTGAAATGGCTAA | 5336 |
| rs183333698 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890777 | TGTAACTTGAAATTT[A/C]CTGCCCTTTCAACAT | 5336 |
| rs183360397 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867922 | GCCAGGATGGTCTCG[A/G]TCCTCTGACCTCGTG | 5336 |
| rs183364531 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911842 | ACATTCTGTTGCCTA[A/G]GCTAGAGTGCAGTGG | 5336 |
| rs183387748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846295 | GATTCATGCTCCAGA[C/T]ATCCCCCCGCCACTC | 5336 |
| rs183403696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885943 | ACTAAGTTTGAGGGA[A/G]GAAGTAAAATGAAGG | 5336 |
| rs183410173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844725 | AAGAGTTAATAAGTT[A/G]TAGTAGACATTCAGA | 5336 |
| rs183411773 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863495 | TGGCAATTGTGAATA[C/G]TGCTGCTGCGAACAT | 5336 |
| rs183450252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899851 | GTCTTTAAACAGAAA[A/C]ACACATAAAACAACG | 5336 |
| rs183457029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886279 | TGGGGCCAGGAGAAA[A/G]TGTAGGAAATCTCTC | 5336 |
| rs183464875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918513 | ACAGACTGTCCTTTC[C/T]CCCTGGTGTGTTCTA | 5336 |
| rs183472687 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877419 | GAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCG | 5336 |
| rs183475594 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904933 | CACTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGT | 5336 |
| rs183495914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864285 | AAGCAGAACTCTGGG[A/G]CTGCGCTGTCCAGCA | 5336 |
| rs183498847 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850084 | AAACAAGGAGACTCC[A/G]TAGGATTGAAGATGT | 5336 |
| rs183502819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949943 | AATGCTACATCTGAT[A/G]TTAAAGGAAACTGTG | 5336 |
| rs183513361 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961858 | TCAATATAGCAATGT[A/G]CAAGAAGATAGAGAT | 5336 |
| rs183517784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929191 | TCTGATGTGTGCTGG[A/G]TTTCCTGGGTCTTGA | 5336 |
| rs183525841 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780260 | GGGCAAGTTGAAGAA[A/C/T]CTTTTTGAGTCTGTT | 5336 |
| rs183528336 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917572 | CTCCTTTAGCTAATA[G/T]CCATTCTAACAGGTG | 5336 |
| rs183536365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802630 | GGGCTGGAGTGCAGT[A/G]GCGCAATCTCAGCTC | 5336 |
| rs183537206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822164 | CTCTTAGCTTTGTCA[A/G]TTGTGGTGGGGTGTG | 5336 |
| rs183555094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824080 | TGTCCTGTCCTGTCC[C/T]GTCCTGTCCTGTCCT | 5336 |
| rs183581118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942258 | TTGATGATAAAACCT[C/T]GTTACCTTAATGGGC | 5336 |
| rs183590720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925015 | TGGTGCGCACTGGGT[G/T]GGTGACTAACAACAT | 5336 |
| rs183619534 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899428 | ATTGGTGGATTCTAC[A/T]TGCTAAAATTGACTT | 5336 |
| rs183630259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939050 | CCTCTTGCCCACATG[G/T]TTCAGCTTGAGGAGG | 5336 |
| rs183639327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921676 | TGTAATTTCATGCAG[A/G]TAGGGATGGATTTTA | 5336 |
| rs183640182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877320 | AATTAGCTGGGCATA[C/G]TGGCGGGTGCCTGTA | 5336 |
| rs183640764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896546 | TTGCGCCACTGCACT[C/G]CAGCCTGGGCAACAG | 5336 |
| rs183657454 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875044 | TCTTGATTCACTGCA[A/T]CCTCTTCCTTCCGGG | 5336 |
| rs183658399 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787724 | TACCTTTCACCATCA[C/T]CCCATCCCCTCATCC | 5336 |
| rs183661269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849627 | CACACACAAATTTTC[C/G]AGGTCTGGTGGCGGA | 5336 |
| rs183673821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797798 | TGACCTTAGGCAATC[C/T]ACTTGGCCTCTTTGA | 5336 |
| rs183677259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808997 | TCTACCAGGCATTGT[C/T]CTCTAAAATATAATA | 5336 |
| rs183678724 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846717 | TGGCTTCATCTATAG[A/C]TTCAACACAATCCCA | 5336 |
| rs183683443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820226 | ACACATGTGTAGACA[C/T]GTGTAACCACCACCC | 5336 |
| rs183722347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884244 | TAATCCCAGCTACCT[A/G]GGAGGCTGAGGCAGG | 5336 |
| rs183735169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875184 | GGCCAGGCTAGTCTC[C/G]AACTCCTGACCTCAG | 5336 |
| rs183743773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859992 | TATTATTTTTTAGAG[A/G]CAGGGTCTCTGTCTG | 5336 |
| rs183746244 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847242 | AAGAGATGCATAGGG[C/T]ATAGGGTTCCCATGT | 5336 |
| rs183754591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791601 | TCAGACGGAATCTCT[C/G]TCACCCAGGCTGGAG | 5336 |
| rs183755474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834189 | AAATGGGGCTTTCTT[A/C]CCAAGATTGGTGGGA | 5336 |
| rs183771201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812926 | ACACCATTTATTAAG[C/T]AGGGAATCCTTTCCC | 5336 |
| rs183852836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909376 | GGTTAGGAAAACCTT[C/T]CTGAAAGAAGATGAG | 5336 |
| rs183857519 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81948467 | GTTCTGTTTTGTGCT[A/G]GGTAGGAGCTAACCT | 5336 |
| rs183863961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927455 | AGTGAAAGTGACCAA[A/G]TGGGGAATTTGTCCT | 5336 |
| rs183869763 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884086 | CCGGGTAGGGTGGCT[C/T]ACGCCTATAATCCCA | 5336 |
| rs183872111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815941 | GTGACTTGCGCCTGT[A/G]ATCCTGGCTACTCAG | 5336 |
| rs183892919 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777610 | GAGCACAGCTATACA[C/T]GCCAGTTGGGAGTGC | 5336 |
| rs183894659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859898 | ACGTATATTCAGTTT[A/C]CTTGACTTTTTCACT | 5336 |
| rs183895926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789956 | CTCCGTGGAGCCTAT[A/C]TTGCTTTATTAGGTA | 5336 |
| rs183905857 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833370 | CTGGACTGTGGCTCC[A/G]GTCGGTACACGGGTC | 5336 |
| rs183914399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945968 | TTAACCTTGCTTCCC[C/T]GTATGGACCAGTCAG | 5336 |
| rs183935320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925610 | CCAGAAAGGTCAGCC[A/G]GGTGCAGTGACTTGC | 5336 |
| rs183963322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900243 | TGTTGGTGACCCTGG[A/G]TGAAGCACACATGGG | 5336 |
| rs183966529 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882323 | TAGTGTTCCCTACCT[A/G]ATACCTAACCTCTGC | 5336 |
| rs183970415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872821 | CTCCTCTGTGCAATG[A/G]GAGGTTGGGAGTTGT | 5336 |
| rs183977423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857903 | TGGGATCAATATAGG[A/G]AAAACACTTAGAACA | 5336 |
| rs183981239 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886734 | CCTCTCCTCTGTTTC[C/T]CCATTTATATAACAT | 5336 |
| rs183981563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782000 | CCTCAGCCTCACGAG[C/T]AGCTGGGATTACAGG | 5336 |
| rs183986270 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845246 | GTTCCCTGTCCCGTG[C/T]TATTTCTTATGCCTT | 5336 |
| rs183992168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830782 | AGGAGACTGACAGAC[A/C]CAGTGTGTGATAGTG | 5336 |
| rs183995672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793159 | CTGGCCTCCAGGTTC[C/T]CTATTGCTTTCCAGG | 5336 |
| rs184001484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804197 | CTCCAACTTCCCCAT[A/G]TCCTCGCCAACACAT | 5336 |
| rs184004379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814227 | GCTGTCTTTTTGCTT[C/G]TTTTCTGGTTATTTC | 5336 |
| rs184007236 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789284 | CACTCGCTTACGCGG[A/G]TGCGCTCTCTCGCTC | 5336 |
| rs184007573 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880462 | CACTTAAAAATAATA[C/G]TAGATGTTACAAAAA | 5336 |
| rs184019091 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855396 | TTGACTTAGAAGTAT[A/G]TGTATATTAATTAAG | 5336 |
| rs184019473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825662 | TGCAGTTTAATTGTA[A/G]CTTTAATGGCAAAAA | 5336 |
| rs184041296 | snp | A/C | 0.181978 | 0.240568 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805514 | AGAAAAAAAAAAAAA[A/C]AAAACAAAACGCAAG | 5336 |
| rs184056501 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827018 | TCCAGCCTCCCTGTT[C/G]CCCTAGGGAATTTCC | 5336 |
| rs184079707 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853504 | CTTTAGGATAAAACT[A/G]TTCTACTTCAGATCA | 5336 |
| rs184087323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841924 | AAGTGAAACCACCAG[C/T]AGCTGGGAAGCTGGT | 5336 |
| rs184092108 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936791 | TGGACACAAAGTGAT[C/T]GCATAAATCACGGGG | 5336 |
| rs184093710 | snp | C/T | 1.65999e-05 | 0.00288091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957945 | TGATGGTGAAATCTG[C/T]TTTATTTCAGGTTAA | 5336 |
| rs184114714 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912018 | TAGCCAGGATGATCT[C/G/T]GATCTCCTGACCTCA | 5336 |
| rs184148700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892067 | AACCACAGAATAGGA[A/C]TTGCTGATGTGGGGA | 5336 |
| rs184164538 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870728 | AATGTGGTCATAGCT[A/G/T]TCTCTTCAGCATGCC | 5336 |
| rs184182341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843804 | TTGTCAGAAGCAAAT[A/G]CTGGGATGAAAGAAG | 5336 |
| rs184190327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935420 | TGGACATCTTTGGGG[A/G]CCATTTAAAAAAAAA | 5336 |
| rs184191592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955977 | TTTATAGCCTATTAC[A/G]TGTTGTACAGTCATG | 5336 |
| rs184198391 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944749 | CCCAAGTGCTAGGAT[A/T]ACAGGCATGAGCCAC | 5336 |
| rs184203695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922679 | TGAGGAAAAATTTTA[C/T]TAGGTTCCCTGTGAA | 5336 |
| rs184214447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785105 | GATCCTAGGAGGAGC[C/T]GGTGAAAGGGTGAGA | 5336 |
| rs184214889 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897282 | CTTTCTGGGGTAGAA[G/T]AGCAGTTACGAGTAT | 5336 |
| rs184217795 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795647 | TGGCTCAGGAGGTTG[C/G]AGGTTTCTATGGGCC | 5336 |
| rs184218091 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910801 | TGGCCTGGTGGTTCA[G/T]CCGGGCCAGTCCCCC | 5336 |
| rs184218955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891299 | ATGTCGCTGCAGCCC[A/T]TTGCAGCCTGAGCCT | 5336 |
| rs184220726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814517 | GGCCAAAATGGTGAA[A/C]TCCCATCTCTACTAA | 5336 |
| rs184221164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884372 | CAAAAAACAAAAACA[A/C]CCCCACCCCACCAAA | 5336 |
| rs184221719 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806065 | TTCAACATGTATGCA[A/G/T]TATAATTATTAACGA | 5336 |
| rs184225611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934975 | GTCCCTCCCATAACA[C/T]GTGGGAATTATGGGA | 5336 |
| rs184227668 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778354 | CAGCCTGGGTGACAG[A/C]GTGAGACCCTGCCTC | 5336 |
| rs184231077 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816173 | GTCAGGAGTTCGAGA[A/C]CAGCCTGGCCAATAT | 5336 |
| rs184238285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875346 | GCCATTTTAGGGATT[A/G]AGAAACTGAGGTCCA | 5336 |
| rs184238553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827487 | AGTCACTGTACCCGG[C/T]CTGCATTTATTTCTT | 5336 |
| rs184248322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868756 | ATCTGGTCATTTGAC[A/G]TCATTTTCTGCCCAC | 5336 |
| rs184289274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850931 | TTTTTGTTTCCTCGA[A/G]GTCTGCAATCAGTGG | 5336 |
| rs184293288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843262 | GACCATCATTTGCCC[A/C]TCTCCTTCTCACTAG | 5336 |
| rs184296889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839310 | GAGAAATAATGTCAT[A/G]TGGCTCCAAACCACC | 5336 |
| rs184360944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922035 | GATGAGAACAGTCAC[A/C]TCTCTAACTGATGAC | 5336 |
| rs184364683 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903919 | TGAGGTGGAAATAGC[A/C/G]TTGGCCACACGGTCA | 5336 |
| rs184375195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826028 | GTCTGGTCGCACTGG[G/T]TATCTAGTAAATATT | 5336 |
| rs184391285 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943193 | TAGACTGTATTAGTC[C/T]GTTCTCACACTGCTA | 5336 |
| rs184393918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879906 | GGAGCTGAAGCAGTC[C/T]GATATTTCTTTCGTC | 5336 |
| rs184395773 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958749 | GCTCTGCCAGCTGCT[A/G]GGAGGCTCTGGCCCC | 5336 |
| rs184401908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896851 | TTAACAGATGAGTAA[A/C]TTGAGACAAGGAGGG | 5336 |
| rs184403748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932592 | CTCCAAGATAGTCAC[A/C]CACCAGTGGCCAGGT | 5336 |
| rs184409507 | snp | A/T | 0.00011597 | 0.0076139 | missense | PLCG2 | GRCh38.p7 | 16:81854452 | ATTTTAGTGGATATC[A/T]TGGAAATAAAAGAAA | 5336 |
| rs184418378 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920353 | TGTTCTAGATACTAG[C/G]AGTACTGTGGAACAA | 5336 |
| rs184429960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894598 | CAACAACCAGCTTGT[C/T]GTGGTGTCTCATGCC | 5336 |
| rs184432738 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947032 | CCCCTCCGCAGACAC[C/T]TCACAGAAAAGTCAA | 5336 |
| rs184433043 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907217 | CTCCTCTCACATTAA[C/T]GTCATGCATGACAAT | 5336 |
| rs184445159 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781924 | TCGCCCAGGCTGGAG[G/T]GCAGTGGCGCGATCT | 5336 |
| rs184477337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785727 | AACGGTTGGGTCCTT[G/T]AGGTCAGGGGCTCTT | 5336 |
| rs184477931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916973 | AGTCCCTATGCTGTA[C/T]CATAGATCTCTTGCA | 5336 |
| rs184482927 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942893 | CCCAGTGAAATGACT[A/T]GAAACAAGAAGAAGA | 5336 |
| rs184486203 | snp | C/T | 8.28823e-05 | 0.00643695 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928518 | TTCTTTTTATTATTC[C/T]CGTTACAACTAACGT | 5336 |
| rs184492087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903597 | GTTTGCACCCAGGCA[A/G]TTGTTTCGGAGATGC | 5336 |
| rs184495733 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806618 | ATAGCCTGCAGACAT[A/G]TGATTCGTGTCTTGT | 5336 |
| rs184502050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920106 | GGAAGTCAGCATGGC[C/T]GGAATCAAGCCAGCC | 5336 |
| rs184509472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879633 | TAGGAGATGTTTTAT[A/G]TCGTTAGCATTGATC | 5336 |
| rs184511553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891160 | AGAGCATGACTCAGT[A/G]TGAAAAAACAAAGAA | 5336 |
| rs184515668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827898 | GAGTTCAAGTCCAAC[C/T]TGATCAACATGGAGA | 5336 |
| rs184526691 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868184 | TGAGCCCTGGGGGTC[A/G]ACCATGTGTACTTTG | 5336 |
| rs184531682 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854016 | ACTCAAGGGAAAAGG[C/T]CATCAAGGTCAAGGT | 5336 |
| rs184534778 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894301 | GTGTGTAGTGGCATG[C/T]GCCTGTGGTCCCAAC | 5336 |
| rs184539874 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842380 | TGGACAGGGCCTGTC[A/C]TCCCTCCCAGACTCG | 5336 |
| rs184556174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877539 | AGGTGTTGGCAGGGC[C/T]ACACCCCTCGGAAGG | 5336 |
| rs184620404 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796169 | GGACTTTCCTGTCTG[C/T]AACTAGAGCTGCTGA | 5336 |
| rs184631286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953012 | CTTCCTGAGGTGAGA[C/T]GCTGAGAAGGGTACA | 5336 |
| rs184639514 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817098 | CTGGTGGGGAGAGAC[A/G]GATGGTAAACAGGGA | 5336 |
| rs184640965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956050 | CCTCACGCTCATTAG[C/G]TGCTGCCACTCACTC | 5336 |
| rs184642651 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932420 | CGATGATGGAGTAAG[G/T]GCTGTCTGTTCTTGT | 5336 |
| rs184645442 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906909 | TGGGCATGGTGGCAC[A/G]TGCCTGTAGTCCCAG | 5336 |
| rs184673217 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944869 | GATATCAAGGGCCAA[C/G/T]TGTAGAGTAAAAGTT | 5336 |
| rs184691292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809372 | CACCCTCAGTCAGGA[C/T]ACTCCTGGCTTGTTC | 5336 |
| rs184696091 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820590 | ATCTTGGGCATATCA[C/G]TTTTCCCCTCTGTAT | 5336 |
| rs184705898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864594 | TAATAGTTCCCGCCT[C/T]CCAGGGCAGATGTGA | 5336 |
| rs184710210 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952869 | CCCAAAAGTGTCTTC[A/C]GCCAAGAAATTTATC | 5336 |
| rs184719035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839071 | TTCTAGGTAGAATTT[A/G]ATCATATTGTCACGT | 5336 |
| rs184722499 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942640 | CTTTTAATCCTCACA[A/G]TAATCCTGTGAAAGG | 5336 |
| rs184732759 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950400 | ATTAGCAAATAGCAT[A/G]GTACCTAAGTATATA | 5336 |
| rs184736226 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901061 | TGCAGAATGCGTGCA[A/G]CTGCGCCTGTCATGT | 5336 |
| rs184736406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932233 | GGAGGTCTGGAATTG[A/G]GCAGACTGGAGTTTG | 5336 |
| rs184738021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913718 | GCGCGGTGGTGCTGG[C/G]TGCATGGCAGCTACT | 5336 |
| rs184747574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919977 | TGAAGTTTTCAGAGG[A/G]TGGTCTAGGAAGATC | 5336 |
| rs184750238 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797394 | TTGTCTTGGGAGAGA[A/T]TTAGGTGCTGTGCAG | 5336 |
| rs184751775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887716 | CGCATATTTGCTTCT[A/G]TTAGTCATAAAGATA | 5336 |
| rs184755786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878226 | CCTGACCTAGTGATC[C/T]GCCTGCCTCGGCCTC | 5336 |
| rs184759520 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865425 | TGAGGCTGTCCCAGA[C/G]CTAGGAGCCCAAAGA | 5336 |
| rs184766861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851390 | TTCTTGTTATTTTGC[A/G]TTTGTTTTGGTGTGT | 5336 |
| rs184770312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839472 | ATTAATAGGCTGTAT[A/G]TAAAGTAATGAGCCC | 5336 |
| rs184779605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819568 | ACTCTATCCCAGCTC[A/G]GTTATTTATGTATTT | 5336 |
| rs184843851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860566 | TGTTCATCTGCAACC[A/G]AGGCAACCAAGTGTT | 5336 |
| rs184867194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834324 | CTCGGAGGGCTCGGT[A/G]TTCTGCTGGCTGCTG | 5336 |
| rs184871816 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787266 | TCTTTCTTTTACCCA[C/G]GCTGGAGTGCAATGG | 5336 |
| rs184877892 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961971 | GTCACCCCATTGATC[A/G]CCAGGGTTGATTCGG | 5336 |
| rs184887553 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808833 | CCATAGCCTCTGTGG[A/G]CCTGGCCTCTGTTTC | 5336 |
| rs184923289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785916 | TCAGTACTAAAATCA[A/G]TTCACTCTTTAATTC | 5336 |
| rs184923472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811774 | CAGTCTATCATCGAT[A/G]GGCATTTGGATTGGT | 5336 |
| rs184927659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796328 | TGGTTTTGCAACCTC[C/T]CAAGGATGGACCCCT | 5336 |
| rs184935667 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822820 | AGTAGAAGACAATGG[C/T]AAGATGATGGCAACA | 5336 |
| rs184939672 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806931 | CCCAGGGCTGTGGAG[G/T]CCTCCATAGCACTCA | 5336 |
| rs184960761 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898540 | TTTATTTTTATCATC[G/T]TCACTTTATTTTCAC | 5336 |
| rs184967747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847470 | CCCTCTAATCACATC[A/G]TTGGTTCCCCTGGCA | 5336 |
| rs184968819 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911206 | AAAAATGTCCATTTC[C/T]GAGGAGGCCGTATTA | 5336 |
| rs184979590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885027 | CGAATAGCTGGGACT[A/G]CAGGTATGTGCCACC | 5336 |
| rs184981683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876258 | GAACTCCTGGGCTCA[A/G]GTGATCCACCCGCCT | 5336 |
| rs184985755 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788622 | CCTCATCTATGCTGC[A/G/T]TGGCTGCTGAACTTG | 5336 |
| rs184987916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800377 | ATCCTTACCCTGCTC[C/T]CCAACAGGCCCTGGT | 5336 |
| rs184998653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861904 | TCGGCTGGTCCAGGA[C/G]CCTCTGCAGAGAGAA | 5336 |
| rs185003953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809883 | GAGAATTTACTGGAA[C/T]GTGTGGCTGAGATGC | 5336 |
| rs185005979 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848144 | ATAGAAAGATTAGTA[C/G]AACAGGATCAAGAGC | 5336 |
| rs185008398 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821896 | TTTTCCAGAGCAGCA[C/G]AAAGAGAGAGCCAGA | 5336 |
| rs185012340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836646 | CTTAGGAGACTGAGG[C/G]AGGAGAATCGCTTGA | 5336 |
| rs185040452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953090 | ATAAGAAGACACCAG[A/G]CAAAAGTTGCTGGAC | 5336 |
| rs185043432 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790935 | CAGAGAGTGATCCAG[C/T]AAACGTGTCAGTGGT | 5336 |
| rs185070425 | snp | C/G/T | 1.68337e-05 | 0.00290114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937935 | CTTCCTGCCAGGGGA[C/G/T]CCAGCCGCCCTCCCT | 5336 |
| rs185080801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913019 | CTGAGGCACAGCAAG[A/T]TTAAGTAACTTGCTG | 5336 |
| rs185089332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887151 | TTGAGATGGAGTCTC[G/T]CTCTGTCACACAGGC | 5336 |
| rs185108235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864972 | ACAGCCCTAGGTTGA[A/G]CTCCCAGGAAACATG | 5336 |
| rs185122796 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962842 | ATTTATCCCACGTTT[C/G]TTTGGGTTACAGGTT | 5336 |
| rs185154021 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930071 | GCCTAGCAAAAGCAG[A/G]GTGCCTTTAGTCTCA | 5336 |
| rs185169536 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802261 | GGGATTACAGGCGCC[C/T]GCCACCGCGCCCAGC | 5336 |
| rs185171698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926344 | TCCCTGGCTGCGGAA[A/G]ATAGCTCAAGAGATG | 5336 |
| rs185179448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947902 | ATCTTGGTAGATTTC[C/T]ATTGCCTTATGATTT | 5336 |
| rs185185020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822996 | AGCCCAGTGAGACTG[G/T]TTTTGACCTAGGAGC | 5336 |
| rs185193591 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959341 | TACTGCTGAAAAGCA[C/G]GGCAGAACAAATCAG | 5336 |
| rs185203416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938537 | GGGCATGGATGTGTG[C/T]ATTCATGAGCTCAGG | 5336 |
| rs185204267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900376 | ATACAGAGAAAAGGT[A/G]CATTCTGGGGTATGG | 5336 |
| rs185208037 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914384 | GCAGAAAGGATGGCC[C/T]CCTCCCTGAGCCAGG | 5336 |
| rs185209849 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778986 | TAAGTATACGGCAAA[C/T]ACCTGGACTGCGGCC | 5336 |
| rs185215522 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883688 | CTTTTCTGGCCATCA[C/T]CTCAGGTGTCACTGC | 5336 |
| rs185215805 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895636 | TTGCATTATGTAAGC[A/G]CACAGGGAACCCTGC | 5336 |
| rs185216680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926903 | CATTAGTAATTAAAA[A/T]ATAAAAAGACAGCAG | 5336 |
| rs185220910 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791258 | TGTCCATTTGGATGT[G/T]GGGGAGGTGGTGAGG | 5336 |
| rs185221387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877775 | GTGTAGATGTCATTG[C/T]ATCGCTCCTTGGCTT | 5336 |
| rs185227129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901517 | CTCAGGGCAGCAGTT[C/T]TCAACTGGGGTTTCA | 5336 |
| rs185229250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874452 | CCCAAGCTATGTAGA[A/T]GGCTTCTGGCCAGCT | 5336 |
| rs185234329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802372 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 5336 |
| rs185238046 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859041 | TTTTGTGCACATTCC[A/G]TAGGACTCACTTAGA | 5336 |
| rs185238263 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812250 | GAGACGAAGTTTCAC[C/T]GTGTTAGCCAGGATG | 5336 |
| rs185249066 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823604 | GATCATAGCTCACTG[G/T]AGCCTCAAACTCCTG | 5336 |
| rs185253039 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832268 | CACCATCAGAGCCTC[C/T]CTCCTGGGCTCCGCT | 5336 |
| rs185296269 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961605 | TACAAATTCAAGGAG[C/T]AAAAGGAAAAGTGGG | 5336 |
| rs185299615 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803946 | CTTGCCTCCCAGAGT[G/T]CTGGGATTACAGGTA | 5336 |
| rs185305788 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787972 | TCAGTCATCTGTTGA[C/T]GGACCCTTGGGTTGT | 5336 |
| rs185307548 | snp | C/T | 0.00622941 | 0.0554608 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81923532 | CAAAGCCAAGCGAAG[C/T]GATGAGCTGAGCTTC | 5336 |
| rs185319999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825120 | TAGCCCAGCGAGACC[C/T]GTTTTGGAAATCAGA | 5336 |
| rs185340215 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897638 | GCAACCTCCACCTCC[A/T]GAGTTCGAGCAATTC | 5336 |
| rs185350481 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875898 | TGAGCGTTCTGTGAC[C/G/T]ATGTTTGTGGAGGAG | 5336 |
| rs185415243 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792849 | AGATGAGATTTGGGT[C/G]GGGAGAGAGCCAGAC | 5336 |
| rs185424196 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949427 | ATAAGTCTAATATCA[G/T]ACTTGTCCTCTTTGG | 5336 |
| rs185424637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957515 | AAGAATGGGCTAGTC[C/T]AGCGGCTCTAGACTG | 5336 |
| rs185432732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945608 | GGCTCCAACTTGCCC[C/T]CCTCAGCCCCAAATA | 5336 |
| rs185434286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813932 | GGAAGGGAAATAGAT[C/T]CTACCTGTTGATGGG | 5336 |
| rs185434533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935841 | TTCTCCTACCCAAAA[C/G]CATTCCCATTCTCCC | 5336 |
| rs185440313 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911134 | TCAAGGTAGGTCTTG[C/G/T]GAAGGGTCAACAAAT | 5336 |
| rs185442316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798751 | GCAAAATTAGGCAAG[C/G]CATGGTGAGAGCATG | 5336 |
| rs185453240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936057 | CTTGAATGTCAAAGA[A/G]GGAGATTCCTGGTTT | 5336 |
| rs185463456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911522 | GTCTCGCAGCAGCCT[C/G]GAGCTCCTGGGCTCA | 5336 |
| rs185467960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884711 | TTTACTTCATTTGTT[A/T]TTTTTTAAATAGAGT | 5336 |
| rs185469208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924444 | TAACTGAGTCTACAT[C/G]ATGACTGTAAAAGGT | 5336 |
| rs185471168 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899139 | GGTTGCAATGAGCTG[A/C]GGTCACGCCATTGCA | 5336 |
| rs185476028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861028 | CAAAAAAACCCACCA[C/T]GACAAGAAAAAACCA | 5336 |
| rs185534731 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778090 | CACACACAAAAAAAA[C/T]GCTATAACAGACCAG | 5336 |
| rs185542116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947673 | CCCAGAAAACTGTCA[A/G]TAAGCACTTTACACA | 5336 |
| rs185576877 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926494 | TAGTGTTGTTATAAA[G/T]ATAGGGAACAATGTT | 5336 |
| rs185587786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817316 | TACCTGTGCCGTGAG[A/G]CAGTTGTGAAGGTAA | 5336 |
| rs185613022 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906114 | TAACCATAGTATAAT[G/T]AGCGCAATCAGGAAA | 5336 |
| rs185616486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882149 | GGCTCCTGCAAGTGC[G/T]CAGGGAAACATACCC | 5336 |
| rs185639904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857282 | TTCTCCTGAGCAGCT[A/G]GGGTTGAGAAACTCT | 5336 |
| rs185655633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829858 | ATGGGGAAGGAACCT[C/T]TGAGTGGGGGGGCGT | 5336 |
| rs185667569 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958842 | GCTCTCCACAGGCAA[G/T]AGGTCAACTGCTGCT | 5336 |
| rs185675011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954994 | CTCCACAGCCTCGCC[A/G]GCATCTATTGTTTCC | 5336 |
| rs185687593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790142 | AATGAGAAGATGCAT[C/T]GGAGAGGCTCGGCTG | 5336 |
| rs185690018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938071 | TCTTACAGTACACTC[C/T]GGGGTCGTTCTGGGA | 5336 |
| rs185715002 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959658 | TGAAGAAAGAACATT[C/T]CTCTTAGTGGCAGAT | 5336 |
| rs185731450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828066 | TTGCACTCCAGCCTG[C/T]GCAACAAGAGCAAAA | 5336 |
| rs185739725 | snp | A/C | 0.00115945 | 0.0240498 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81893772 | CATCCGCTGCCTGCG[A/C]ATGGGCTGTCGCTGC | 5336 |
| rs185747646 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869454 | AGAGGGATCATGGAC[A/G]TATCTGAGGACCATC | 5336 |
| rs185749455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793795 | GTCCAGTGAAGGGGG[A/C]GCTATCCCTGCTTTA | 5336 |
| rs185752566 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805227 | ATAAAAGGCCAGGCT[C/T]GGTAGCTCATGCCTG | 5336 |
| rs185758840 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854927 | AGGCTCTGTTGGATG[A/C]AAAATGTACGCTGGG | 5336 |
| rs185764208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871941 | GCATGTGTCAGTTCT[C/G]TTTCCATTAATCTGA | 5336 |
| rs185764541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815212 | AAGGGAGGAGGTTTT[A/G]TTGCATATGGGGCCT | 5336 |
| rs185765854 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843543 | AAGTACCTAAAATCA[G/T]CCTACCAATATTTTT | 5336 |
| rs185771903 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826653 | CCACTCATTAACCAC[A/G]TCCTCTCAGTGGTCT | 5336 |
| rs185782654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845047 | AATTCTCCTCCCTCA[A/G]CTTCTTGAGTAGCTG | 5336 |
| rs185783519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956414 | AAACCGGGTTAGATT[A/G]AGAAATAGGATCTAC | 5336 |
| rs185805710 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935922 | GTTTAAAAAAAAAAG[A/T]AAATTACAGTAATTC | 5336 |
| rs185811797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918685 | GTAAGATAGTGTGCT[A/G]TCTGCAGCTTTGTTA | 5336 |
| rs185819419 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892120 | GTGTTTCAGACAGAG[G/T]AGCAGCATGTGCCAA | 5336 |
| rs185837323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793428 | TTTTGTCTCAGGAGC[C/T]GATGTGGTGCCACCT | 5336 |
| rs185862048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844069 | ACAAGCTCTGCCTCC[C/T]GGGTTTATGCCATTC | 5336 |
| rs185909186 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933436 | TCTGTAGCCACCTCA[C/T]TGATGGCAGAGGGCA | 5336 |
| rs185948553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945334 | TTCAAGACAAACTAG[A/G]ACCACAGAAACCATC | 5336 |
| rs185950474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924394 | GTGTCAAGCACTGTT[G/T]TAAGCACGTTTGAAA | 5336 |
| rs185958507 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957576 | GTTGTGCTACAGGCA[C/T]GTAATGGGGTGCGGG | 5336 |
| rs185960987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880691 | GGGTGACTGCTTCTT[C/G]GGAATACGACTGTGG | 5336 |
| rs185968789 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782835 | GACATTACTGCTGCA[C/G]CTTACACCCACCCTG | 5336 |
| rs185982486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804438 | GACTAGGGCGTAAAT[C/G]AATGAGGCAACTCTG | 5336 |
| rs185982762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855627 | TAAGAAGCTCTCAGT[C/G]GACTTGGGGAGACAG | 5336 |
| rs185992481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796525 | GGTGGGTGCCTGTTA[C/T]GGATTGAATTGTCCT | 5336 |
| rs186004655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807508 | ACTGTCACTAACGCC[A/C]CCATAAGAGCTGACA | 5336 |
| rs186006660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883040 | AGCTAAATGTAGACA[A/C]CAGGGCCTGCCCCTT | 5336 |
| rs186006811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851673 | CTGTGCCACCAAGCC[C/T]AGCTACTTTTTGTAT | 5336 |
| rs186008553 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780528 | TGCAAAGGTGTGTGT[G/T]CAGTCACGTGTATAC | 5336 |
| rs186008940 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873791 | ATATTAAAAATTAAA[A/T]AAAGAAGATTTGCAC | 5336 |
| rs186014645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817472 | TCTTGAGGGGTGCTG[C/T]GCAAGGCACTAGGGT | 5336 |
| rs186014805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791692 | ACCTCAGCCCCCCGA[A/G]TAGCTGGGATTACAG | 5336 |
| rs186016676 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840894 | GGCTGAGTATCCTCA[C/G]TTCCTTTTTCCAGGG | 5336 |
| rs186021139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828420 | TTTTTTTGTATTTTT[A/G]GTAGAGACTGGGTTT | 5336 |
| rs186066690 | snp | A/C/G | 1.81757e-05 | 0.00301455 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921158 | AGGGCTATTCCAGGA[A/C/G]CATGGATTATTCCAT | 5336 |
| rs186070156 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943628 | TCTCAGGCCTCACCC[A/C]AGACTTCCCAAGTCA | 5336 |
| rs186070950 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821982 | AATTCCTTAACTTCG[C/G]TGAGCCTTCTCTTTT | 5336 |
| rs186071307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836124 | CCACCAAGGACAAGA[A/C]CAGAGTCATTTTCAT | 5336 |
| rs186123301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878343 | CCCTAACCCAGCAAG[A/G]CCTCATCTTAACTTG | 5336 |
| rs186127158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786553 | CCCAAGCCTGCAGAA[A/T]CTCATAGCTTGGTCG | 5336 |
| rs186137997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808085 | TTTGGCTATTATGAA[C/T]AGTGCTGCTGTGAAC | 5336 |
| rs186142075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851535 | TTGTTGTTGTTGAGG[C/T]GAAGTCTCACTCTGT | 5336 |
| rs186166269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954537 | TGTGTTGTTGCCCTC[C/T]CTGTGTCCTCATTGT | 5336 |
| rs186193409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940822 | TCTATATAGTTTCTC[C/T]AGTTTACTTTCCCAC | 5336 |
| rs186209561 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933285 | CCACACTGGGCACAG[C/G]TACCCCTTTTGCGGA | 5336 |
| rs186219684 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908716 | TCCCAGGCTTCATTT[C/G]TCTAGCTCTTCTAGG | 5336 |
| rs186220920 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918183 | TCTTTCCTTGGCTAT[A/G]TAGAAGCCTCTTAGT | 5336 |
| rs186237721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904889 | TGTGGGCTATTTTTA[C/T]TTATTTATTTTTTAC | 5336 |
| rs186248062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880335 | CTTGGCAGAATTTAT[C/G]AAAGCCAATGTGCCT | 5336 |
| rs186249713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891720 | GCACCGCATTCCTTG[A/G]ACTAAAATACACAGA | 5336 |
| rs186251898 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783380 | TTACATATATATACA[C/T]GTGCCATGTTGGTGT | 5336 |
| rs186254961 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888167 | TAAGTGAGATGACCA[C/T]AGGAGGAAGAAAGAT | 5336 |
| rs186255848 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793626 | CGGATTCTCAAACAT[A/G]TGAGCTGTCTGTTTC | 5336 |
| rs186261892 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865688 | CCAGGATGGGCTCCA[C/T]TGGGGCACCAGCATG | 5336 |
| rs186263089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870357 | CCCAAAGCCATAAAG[C/T]AATTAATTGGAGCTG | 5336 |
| rs186263704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855370 | ACTTTCAAGTTCAGT[C/T]CTAGAATTTATTGAC | 5336 |
| rs186265940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804867 | CTTGAAAGCTTGGGA[A/G]CAGTATTGAGCATCT | 5336 |
| rs186281329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818180 | CCGTTAGGATTGCTT[C/T]GGCCCTCTGTGCCTC | 5336 |
| rs186291797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840042 | AGCCTGGGTGACAGG[A/G]CATGACCTTGTCTCC | 5336 |
| rs186326890 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824031 | TTCCTTTCCTTTCCT[G/T]TCCTTTCCTTTCCTT | 5336 |
| rs186329861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831577 | TCCAGTTGGGACCCC[A/T]GGCTGGGTCTCTGAC | 5336 |
| rs186362910 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885401 | ACTCCTGGGCTCAAG[C/T]GACTCACCTGTCTCA | 5336 |
| rs186366823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904412 | AACTTACAGACGCTT[A/G]CCTGCGTGGGAGTCC | 5336 |
| rs186373944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799390 | GTACTACTTTGTGAC[C/T]ATGTTAGTATTATTA | 5336 |
| rs186377096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784226 | GGGCCCCTCCCCATT[A/C]CCCTCATTTGCATCC | 5336 |
| rs186381584 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862972 | CTTCCCTTCCCCACC[C/G]TGACCAATCACCTTA | 5336 |
| rs186384814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880171 | ATGTGAGCTCAGGAG[A/G]GTGAGGCTGTGGTGA | 5336 |
| rs186391277 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820743 | CTCCCACCTCAGCCT[A/C]CTGAGTAGCTGGGAT | 5336 |
| rs186395356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837672 | AAGAACATCTGTTTG[A/G]TACCAACATGTGTTT | 5336 |
| rs186421750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915319 | CTCTGGGGATGTGTA[A/G]TGAACTTCTGGATAG | 5336 |
| rs186429085 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927514 | ATTTATATTGGACAG[C/T]CAGACATTGAGAACG | 5336 |
| rs186429484 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902420 | AAGTTGTAGGCTGCC[A/G]ACTTCTAGTTGTGTC | 5336 |
| rs186430956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953818 | CTACAGTATGTAATA[C/T]AGCTGCAAATATTTT | 5336 |
| rs186434917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932657 | GCCAGTCCCTGGTCA[C/T]GAGAGGATCCTTGAC | 5336 |
| rs186437475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943301 | TTTTGTTTCTGGGGA[C/G]GCCTCAGGAAATTTA | 5336 |
| rs186446820 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889682 | GTTTTTGAGATGGAG[C/T]CTCAGTCTGTCACCC | 5336 |
| rs186451692 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878966 | TTCAACAAGCAGAGT[G/T]TCCGGGCAGGGAGTT | 5336 |
| rs186574115 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877225 | TTTGGGAGGCCAAGG[A/C/T]GGGCGGATCGCGAGG | 5336 |
| rs186575368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788264 | TCCTGAAGGTTTATT[G/T]CTGAGCTGAAGGATA | 5336 |
| rs186578915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917935 | ACCATGTTGGCCAGG[C/T]TGGTATCGAACTCCT | 5336 |
| rs186579455 | snp | C/G | 2.15678e-05 | 0.00328381 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938939 | GTCACCTTGGCCCCT[C/G]TGCTTTTAAACGTCC | 5336 |
| rs186580496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891669 | GTCCGATACGCCGCT[A/C]CGGTGAGCCCTGTTG | 5336 |
| rs186596610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809744 | CCCTGATTGGCTAGC[C/T]TTGTCACTTCTGTCC | 5336 |
| rs186599678 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848460 | AGAATTTCATTCTTT[C/G]TTTCTTACCATGCTC | 5336 |
| rs186608105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914548 | GTCTTCCCCATGAGA[A/T]TGGAGGTGTCTTGAG | 5336 |
| rs186629977 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888824 | CCAAATATAGCTGAC[A/C]ACTTGTTTTTATAAA | 5336 |
| rs186631219 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925748 | CAAAAATTAGCCAGG[C/G]ATGGTGGCCCATGCC | 5336 |
| rs186637148 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899855 | TTAAACAGAAACACA[C/G]ATAAAACAACGTCAG | 5336 |
| rs186640236 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912430 | CTTTTCACAAATTCT[C/T]TTTGCTGAGGTGCCT | 5336 |
| rs186642922 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886497 | TAAATAGTTGCCCTC[C/G]CAGACACTTATCCTA | 5336 |
| rs186665909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864309 | TCCAGCAGGGCACCC[C/G]TCACCACAGGTGGCC | 5336 |
| rs186675220 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850123 | AATGAGATAAGATGT[A/T]TGCATTTTATTTGTC | 5336 |
| rs186681306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838673 | TGCAGGGTTTAAAAC[C/T]TAGATGATGGGTTGA | 5336 |
| rs186682959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845829 | GAATACCAGATAGAA[A/G]ACCCTGGAGAGAGCT | 5336 |
| rs186684624 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812942 | AGGGAATCCTTTCCC[C/T]GTTGCTTGTTTTTGT | 5336 |
| rs186723409 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777625 | CGCCAGTTGGGAGTG[C/T]TGAAAGAAATGAATC | 5336 |
| rs186734819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789985 | TATGAGCAGTCTGGG[A/G]CTTGACTTCCAGTGC | 5336 |
| rs186748723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801405 | TGCGTGGTGTGTATC[C/T]CTCAAGCAACTTGCA | 5336 |
| rs186750867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811399 | AAAAGGGAAGGCCAT[C/T]CCCAGTGTTAGTCAC | 5336 |
| rs186762558 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822692 | AACCCGGGAGGTGAA[G/T]GTTGTAGTGAGTGAA | 5336 |
| rs186793140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948156 | GCTAGATATTTAGCA[A/G]TGGAATAATAAATCA | 5336 |
| rs186829827 | snp | A/C | 0.000215583 | 0.01038 | missense | PLCG2 | GRCh38.p7 | 16:81927167 | GCAGACTTCGAGGAG[A/C]TAGAAAAGCAGGTGA | 5336 |
| rs186847811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945692 | TGGCTTTAGGAGGAG[A/G]AAGATCAATACTGCT | 5336 |
| rs186848705 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960721 | GCCGGACAACATGTT[C/G]TAATACTTCGTATGC | 5336 |
| rs186852601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902149 | ATGAGAGCTTAGTCA[C/T]GTTACCTGCAAGGAC | 5336 |
| rs186853424 | snp | A/G | 0.00636936 | 0.0560724 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962743 | CCTTTTATATTCCCA[A/G]ATAAAACACACACAC | 5336 |
| rs186857287 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878792 | CTTTGGGATGCCCGA[C/T]TGTCTTCCTTATCTT | 5336 |
| rs186860350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786418 | CTGAGGTCAGCCAAC[A/G]TGGAAATGGCATTCA | 5336 |
| rs186871776 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925459 | AAATGGTGCGGGGGG[G/T]CGTGAAAAGGGCTTA | 5336 |
| rs186877828 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927630 | CGCCGCCTCTTGTTT[A/G]GAGAGCAGCCACTTT | 5336 |
| rs186884612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949109 | GTCTCACAATCTAGG[A/G]CAACCCCACCATGAG | 5336 |
| rs186885214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802649 | CAATCTCAGCTCACT[A/G]CAACCTCTGCCTCCC | 5336 |
| rs186889553 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939447 | ACTCAGATGCTGACC[A/G]AATAAACTGGCATTT | 5336 |
| rs186889953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910478 | CTGCCGCAATGGCCT[G/T]GCCTGCGTTCTCCCA | 5336 |
| rs186891652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858151 | GCCTTCTGCAAAACT[A/G]GAAACCAGCATAGGC | 5336 |
| rs186893446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916218 | TTCTAGCATTTTGTT[C/T]TTACAGGACTTTTTG | 5336 |
| rs186900688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884307 | AGTGAGCCGAGATTG[C/T]GCCACTGGACTGCAG | 5336 |
| rs186904992 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875195 | TCTCGAACTCCTGAC[C/G]TCAGGTGATCCTCCC | 5336 |
| rs186908253 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831142 | TGGTCACACACCATG[A/C]TTTGCTCTTCTTTGG | 5336 |
| rs186964112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781199 | ACTCTCCTGGATTTA[C/T]CAGAAGATCACCTTT | 5336 |
| rs186972503 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826466 | CTCGACCTCGTGTGC[C/G]TCAGTCTCCTCACTG | 5336 |
| rs186980364 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792102 | AGCAGCCAAGCTCCC[A/G]CATGAGCATGTCGAC | 5336 |
| rs186981004 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809980 | TCTTTGTCTGCCACC[A/G]TGGTTCTCTCCTTTT | 5336 |
| rs186983143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847870 | GAGGCTTGAGCATCT[A/G]TTTGGATTTTGGTAT | 5336 |
| rs186987756 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803070 | CCTTTACAGAGTTTC[C/G]TATTCTGGACATTTC | 5336 |
| rs186991268 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813363 | GAGCAGTTGTTTGTA[G/T]TTCTCTTTGAAGAGG | 5336 |
| rs186997582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824483 | CAGCCTCTGGGGTTG[C/T]GACTGCTGGAAAGCA | 5336 |
| rs187015077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893105 | ACCTCGTGATCTGCC[C/T]GCCTCAGCCTGCCAA | 5336 |
| rs187021687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881668 | ATGTATATTCGAGAC[A/G]GAGCCTCCCTTTGTC | 5336 |
| rs187023553 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871227 | GTCTGTTAAAAAAGT[A/G]CAACTCACTCTACTG | 5336 |
| rs187030332 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856288 | TCATAGTTCCATGAG[A/C/G]TGTTTGCACTGTTAG | 5336 |
| rs187039268 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844272 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 5336 |
| rs187083214 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958386 | GATCCAGGTAACTGA[C/T]GTCCATGGAGGATGA | 5336 |
| rs187096464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950507 | AGAAATCAGCAAAGA[C/G]ATAATATCAAAATAA | 5336 |
| rs187097932 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806101 | TTGATTCTGGTTTTT[G/T]GTCTGTGTCTTCAAA | 5336 |
| rs187105394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816514 | ACACGGTCTCATTCT[C/G]TTGCCCAGGTTGGAG | 5336 |
| rs187110715 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827499 | CGGCCTGCATTTATT[C/T]CTTTAAAATCCTACT | 5336 |
| rs187111664 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937513 | GCTACATAGACACTT[C/T]TAGCAAGTTTGAATC | 5336 |
| rs187113357 | snp | C/T | 0.000132494 | 0.00813815 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81946185 | TTCAGGATTCAGGTC[C/T]GTTCCTCTGAAGAAT | 5336 |
| rs187116990 | snp | A/G | 1.81863e-05 | 0.00301543 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81912678 | GGCCTTCCTGATCCG[A/G]AAGCGAGAGGGGAGC | 5336 |
| rs187124031 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925919 | ATCCAGAAGGATATC[A/C]TATAGAGGGGAAGAC | 5336 |
| rs187155477 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814789 | CTCACTGTTCCCTTG[C/G]TGTGTGACCACAGGG | 5336 |
| rs187158612 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843699 | TTCTTCTATCCTCCA[A/T]CTACCTTGTACTGTA | 5336 |
| rs187159973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948618 | TCCTGGAGGTCCAGG[A/C]CTGGGAGCTGCACTC | 5336 |
| rs187186455 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907889 | TGGCAAGGGGATGCT[C/G]CGCTGAAGAAGCTGT | 5336 |
| rs187208849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883192 | GGGTGGCAGGCTGCC[C/G]CATTGGCTGGCATCT | 5336 |
| rs187210281 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780018 | AATCCCAAAGAGGGC[A/G]TTACCCGCACAGCGC | 5336 |
| rs187214121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943839 | ATGAGAGCAATGTCC[C/T]CATAAACCCTACCAG | 5336 |
| rs187216291 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802415 | CCGCGCCCGGCCTCA[G/T]GTGGGTACAGTCTTA | 5336 |
| rs187225832 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933896 | TCTTCTGAAGGGAGG[G/T]ACCTCCTGAGTCCAT | 5336 |
| rs187227987 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789812 | CTTCTCCCTCCCACT[A/T]TCCCTTTCTTTCTCC | 5336 |
| rs187228488 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858625 | ATTCCTGGGGTATGT[C/G]CTGGGGGAAAACAGG | 5336 |
| rs187243479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921530 | ACCTTTGGGCCAAAT[A/G]GCTTCTAATGAAAAG | 5336 |
| rs187248007 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879383 | TACACATCAACGAAA[G/T]GAAGTACTTCTCAGT | 5336 |
| rs187249675 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896233 | ACTTTCAGAACCCCC[A/G]AAAGAGAGGGAAAGG | 5336 |
| rs187253110 | snp | G/T | 0.0135063 | 0.0812451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909136 | TAGACACAGTACTTA[G/T]GCCAGACAGACAATG | 5336 |
| rs187255417 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867935 | CGATCCTCTGACCTC[A/C/G]TGATCCGCCCGCCTC | 5336 |
| rs187257287 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884034 | CTACATTGCACAGGG[C/T]AGCCCCCCCTACCCC | 5336 |
| rs187263160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853673 | TGCCGGTACCAGTCC[A/G]TGGCCTGGGGGTTGG | 5336 |
| rs187269480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841984 | CCTAGTAGCTAAACT[C/T]ACCTTGGTGGAGCCC | 5336 |
| rs187319260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808652 | GTGCCCGCCACCACG[C/T]CTGGCTAATTTTTTC | 5336 |
| rs187327147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819380 | ACCAACCCTGTGAGG[C/T]GAGGGAGCTCCTGCG | 5336 |
| rs187339504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829389 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 5336 |
| rs187356594 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960365 | GAAGACTAGTAACAG[A/G]CACATTCTGAAAGAT | 5336 |
| rs187359876 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939141 | CCTGTAACTCAAGTC[C/T]GGAATCGTAGGTGAG | 5336 |
| rs187406162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920946 | GGATTTGTGCTTTTA[C/T]AAAGGAACGCAGTGC | 5336 |
| rs187408323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895193 | TCTGTATCATTTCCA[C/T]GGGCAGAAAAGGCAG | 5336 |
| rs187425461 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874052 | GATTCTGCCGATACC[A/G]AAGGTTGACCCCTGG | 5336 |
| rs187426237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952164 | TCTTATTAAAAAACA[A/G]AACACCATGTGAACA | 5336 |
| rs187426940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791482 | GGTCATTTGGTGTCA[C/T]CTCGCCTGGAAGGTT | 5336 |
| rs187439412 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812555 | TTCTTGTAAATTTGT[A/T]TAAGTTCTTTGTAGA | 5336 |
| rs187441573 | snp | A/G | 0.000182181 | 0.0095424 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931570 | GCAGGGCGATCCTCC[A/G]GTGGAGTTTGCCACA | 5336 |
| rs187444994 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936939 | TTAATAAGTCCCCGT[A/G]GAGGCACATGTAGGT | 5336 |
| rs187446555 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958056 | TGTGTTTGCATGTAG[C/G/T]AGAACGTGCCCTATT | 5336 |
| rs187450589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920050 | GAGAGGATAGCATGC[A/G]CAAAGGTCCTGAGGT | 5336 |
| rs187452725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942280 | TTAATGGGCATCAAA[A/G]TGTGTCAATTCATCT | 5336 |
| rs187454354 | snp | A/G | 0.0118883 | 0.0761761 | missense | PLCG2 | GRCh38.p7 | 16:81919590 | CTCGTCAGTTACTAC[A/G]AGAAGCATTCACTCT | 5336 |
| rs187457572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846095 | CTTGTGCTCCATTTC[C/T]CAGCTGCTAGGAGTG | 5336 |
| rs187474545 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905962 | TCTAAGCCTGGCCAA[C/G]TTTATTTTCCTTTTG | 5336 |
| rs187480585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881965 | CCATAATTTCTATGT[A/G]GTATTTTAATGAAAA | 5336 |
| rs187536603 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784896 | GCAGGCAATGTGTTT[C/G]TGGGGATTTGGGAGG | 5336 |
| rs187541055 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795019 | TGTCTTCTATCCTGG[A/T]TGACAACCTTAGAAT | 5336 |
| rs187543240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794468 | GACGCAACCAATGCC[A/T]GAAGTGTCCATAAAT | 5336 |
| rs187551992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805967 | TAAAGTTTTCTAGTT[A/G]CCACATTCATAAAGG | 5336 |
| rs187556785 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816010 | GAGGTTGCGGTGAGC[C/G/T]GAGATTGTGCCACTG | 5336 |
| rs187625694 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812218 | CCGCGCCTGGCTAAT[G/T]TTTTGTATTTTTAGT | 5336 |
| rs187639285 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944568 | CTCCTGGGCTCAAGC[A/T]ATCCTCCTGCCTCAG | 5336 |
| rs187657735 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849859 | TTAGACTAGACAGAA[A/G]GAGAAAAGAATGTTT | 5336 |
| rs187662085 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837914 | CCAGTCTTATTCAGA[G/T]TTTCCCCCATTTTCC | 5336 |
| rs187662518 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922350 | CATCTCAGTTTTCTC[A/G]TCTGCAAAATGGGCA | 5336 |
| rs187676892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945994 | GTCAGTCATGGCTGC[C/T]GGCCTCTGTCCCTAA | 5336 |
| rs187688638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932294 | AACCACACTTCTCTG[G/T]GCCTCAGTTTCCTTG | 5336 |
| rs187693284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906117 | CCATAGTATAATTAG[C/T]GCAATCAGGAAATTA | 5336 |
| rs187697223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902664 | AAAAGCTCTACCCTC[A/C]TTCCCGTTCATGAGG | 5336 |
| rs187699408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944260 | AGTACAGTCAGCCCT[C/T]TGGATCTGTGGACTC | 5336 |
| rs187699588 | snp | A/C/G | 0.000849745 | 0.0205952 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940093 | AAGATGTTCGATTTG[A/C/G]GCTGGCGTTGTACTT | 5336 |
| rs187711106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879201 | CTCCCTCCAGATGTA[A/G]ATAAGCTGGGTGTGG | 5336 |
| rs187711877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955373 | ACTTGAACTCCATCG[A/G]GAAAGGCCAATTGAC | 5336 |
| rs187727381 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853036 | ACCAGGCCTTCTTAA[A/G]TATTAGGCCCCAGGC | 5336 |
| rs187781861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784556 | ACTCTGTAACCTTGA[C/G]AGCTACAGAGTAACA | 5336 |
| rs187794628 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787267 | CTTTCTTTTACCCAG[G/T]CTGGAGTGCAATGGC | 5336 |
| rs187797955 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805295 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGACT | 5336 |
| rs187800685 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787151 | TTTAACTCCAGAGAA[A/G]GGCATTTCATGCTAT | 5336 |
| rs187809913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808957 | ACCTGCCTGATGAAG[A/G]TTGCTGCCTGTGAGG | 5336 |
| rs187816824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796889 | ATTTTTGGTATTTCA[C/T]GAGTGGCAGGCCTAA | 5336 |
| rs187822322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808528 | AGATGGAGTCTCCCT[C/G]TGTCGCCCAGGCTGG | 5336 |
| rs187830528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818795 | ATAAGGGAGGAGTGT[A/G]GAGGGCAGCCTCATG | 5336 |
| rs187908676 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846905 | GTATGGTTTTCCCCC[C/T]ACGCATCAAGCAAAC | 5336 |
| rs187917993 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951246 | TGGAATTACACGTGT[C/G]AGCCACTGTGTCCAG | 5336 |
| rs187918323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833781 | CGGAATTCCTGGGCT[C/T]GAGCTGTCCTCCTGC | 5336 |
| rs187918517 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867590 | AGGCACCACCTAGAA[C/T]AACACCTGTCACCTG | 5336 |
| rs187924375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852328 | CTGAGCCAGGGCACT[G/T]GGGTCATTCCCTGGC | 5336 |
| rs187929470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935271 | TTCTGCTTCCCTATT[A/G]TAAGGACCCTTGTGA | 5336 |
| rs187931176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952949 | ACCATCTTAATCAGA[C/T]GATCAACGTTACCAA | 5336 |
| rs187938074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955856 | CATGCCCATCTCTGC[A/C]AGATGTAATTTATGA | 5336 |
| rs187939681 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942750 | GTAGGACCAGAGCTG[A/C]GATTCAAACCCAGGA | 5336 |
| rs187950188 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930338 | TGTCTGGAGAACCCA[C/T]GCCACATTTCTCTCC | 5336 |
| rs187953681 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901395 | TGGCTTAAAGCACAG[A/T]AGAGTTTATTTCTTC | 5336 |
| rs187956469 | snp | C/T | 0.0066739 | 0.0573795 | missense | PLCG2 | GRCh38.p7 | 16:81905484 | CAACAGGGGGAGCTG[C/T]ACATGTGGGATTCCA | 5336 |
| rs187962968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886769 | AATAACCTGTACCTC[C/G]TGGGGTGGTGGTAAG | 5336 |
| rs187975423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888137 | GCAATAAATGACTTG[C/T]GGAGTTGTGTGGACT | 5336 |
| rs187976833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864721 | GCCGGGGGCAGTGGA[A/G]GTGCCGGCCCAGCCT | 5336 |
| rs187981672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878279 | GTGAGCCACCGTGCC[C/T]GGCCCAAATCTCCCT | 5336 |
| rs187983619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865568 | GTTCTTGAGCAGCTG[C/T]TCTGGCACCCCAGGC | 5336 |
| rs187986104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890660 | TGCATAGGGAAGGAG[A/G]GGAGGTGGAACTGGG | 5336 |
| rs187991883 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839161 | TTTTTGCCAAAAACA[A/T]AAAATCACTCTTAAC | 5336 |
| rs187994351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851466 | GTACATGCACAGGAT[G/T]TAGATGACGTGCTGT | 5336 |
| rs188005486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867691 | TGTTCTCCCTTGCTT[C/T]CCTCCCTTTTCTTTT | 5336 |
| rs188024112 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841759 | GAAGCCCCTTTTGTC[A/G]TTACATGTTCTTCTG | 5336 |
| rs188053526 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801057 | CTTGTCCCAGTGATG[C/G]CTTGATTTTAGCCCC | 5336 |
| rs188068712 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822571 | AGACCAGCCTGGCCA[A/G]TATGGCGAAACCCCG | 5336 |
| rs188080160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797486 | TTGGGGCCAGGCCTT[C/T]GGTAGTCCTGACCCA | 5336 |
| rs188098197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819639 | GCCCAGGCTGTAGTG[C/T]GGTGGCGCTATCTCG | 5336 |
| rs188130356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791318 | CTTGGGTGGAGTTTA[G/T]AGAGATTTGCTAGAT | 5336 |
| rs188147216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802401 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTCAGG | 5336 |
| rs188153955 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812284 | TTGATCTCCTGACCT[C/T]GTGATCCACACGCCT | 5336 |
| rs188156294 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961146 | AGCCTGTAGATTTCT[A/G]AGTCTCTTAGCATGT | 5336 |
| rs188162902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823782 | CAATCCCCTGACCTC[A/G]GTGTCCCAAAGTGCT | 5336 |
| rs188163931 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830018 | CCTTCAAGGAGTGGA[C/G]AGATTAAATATATAA | 5336 |
| rs188179334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939773 | TCTTAGATCTTGGCA[C/T]AGATGCATATTTATT | 5336 |
| rs188185076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950290 | GAAGGAAAAGTTAAC[A/G]TCAATCTAGAATTTA | 5336 |
| rs188192798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940232 | TGTAGCACACAGGTG[A/G]GAGGAAGTGGGTGAC | 5336 |
| rs188200884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924401 | GCACTGTTTTAAGCA[C/T]GTTTGAAATAACTCA | 5336 |
| rs188200963 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961949 | GGGCGATCTGGCTGC[A/G]ACATCTGTCACCCCA | 5336 |
| rs188209014 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929369 | CCTGCTTCTATTGCC[A/C]ATGCTCTGCTTTACA | 5336 |
| rs188214018 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916858 | GGCCAGGCTGGTATC[A/G]AACTGCTGACCTCTG | 5336 |
| rs188214403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890884 | TTGTATATATGAGGC[C/T]GGGTGCAGTGGCTCA | 5336 |
| rs188229099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919395 | TCTAAGGCTGGATAA[C/T]TAGGTTGTATCTAAT | 5336 |
| rs188233167 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941948 | TACTTTAAACCCGGC[A/T]CTGATCAGGGCTGTG | 5336 |
| rs188237366 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900252 | CCCTGGGTGAAGCAC[A/T]CATGGGTGCTTATTG | 5336 |
| rs188247339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877607 | TTCTAGTGGCTGCCA[C/G]CAATGCTTCAAGCAT | 5336 |
| rs188257564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874755 | GTGTCTAACCACCTG[C/T]CTACGTTCCACCTCT | 5336 |
| rs188264342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850847 | AGGACTGGTCATTCT[C/T]CAGATCTCCTGCACA | 5336 |
| rs188272215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846443 | CTCAGGCTCAACTTC[C/T]AGGGAACCAACCTAT | 5336 |
| rs188318098 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797144 | GAGGCAGCATTTGTC[C/G]CTCAAAATAGCACCA | 5336 |
| rs188341154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810491 | GTGGTCATTCTTGGT[A/G]ATGCAGACTGGTGAA | 5336 |
| rs188343051 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795703 | CCTCCCACCTGCTTT[A/T]TTTTTTTCTCCCCAA | 5336 |
| rs188385260 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793206 | GTGCTGGGATTCCTT[C/T]CATCCCCAGCCTTCT | 5336 |
| rs188389280 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804233 | TATCTGTCTTTTTGG[G/T]TATCACCATCCTAGT | 5336 |
| rs188401634 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814235 | TTTGCTTGTTTTCTG[A/G]TTATTTCACTGTTCT | 5336 |
| rs188409828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825891 | AGGCTAAGATTGTCA[C/T]ATAGGGTGTTAGGTG | 5336 |
| rs188411877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860288 | TCGGAAATCATTTCC[A/G]TGTTGATGCACAGAG | 5336 |
| rs188417133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847330 | TCTAAGCCCTGTCAT[C/G]CTGGGTTTTTATGAG | 5336 |
| rs188425155 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834231 | ATGTTGAGGTCAACT[C/G]TGACACCTATTAAAT | 5336 |
| rs188430142 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947928 | GATTTTTTGTATATG[A/G]TATTTCCATAGTCAG | 5336 |
| rs188448125 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959456 | TGGGGGTGTGGATGT[G/T]TAAACAAAAAGCTGT | 5336 |
| rs188448315 | snp | A/C | 0.000581342 | 0.0170392 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927033 | GAGCAGTAGTGGGTA[A/C]TTCATGCCACCTGGT | 5336 |
| rs188477191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949391 | ACTTCCAGCACACTA[A/G]TTGTGTATAAAGGAA | 5336 |
| rs188482861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928155 | CAGGTCATAGAGCAT[A/G]GGTGTTGCTTCCACA | 5336 |
| rs188493312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903278 | CCAAGATACATTGGA[C/T]ACAATCCTTATGTTC | 5336 |
| rs188509973 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899459 | GTAACCCCAAATCAA[A/G]TCTCAAAGCACTCTG | 5336 |
| rs188516148 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857192 | ACCTGTTGATGTCTC[A/C/T]GTCATCCCTCTCTTC | 5336 |
| rs188526276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877372 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGAGGCG | 5336 |
| rs188548832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859572 | CGGAGTCTCGCTCTT[C/T]CGCCCAGGCTGGAGT | 5336 |
| rs188561904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789393 | ACTCCTGGGCTCAAG[G/T]GATCCTCCTGCCCAG | 5336 |
| rs188564785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833217 | CCAGAATGAAAATCA[C/T]CCTTTAAAGAAGGAG | 5336 |
| rs188588682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787221 | ACTCTTTTTTTTTTA[A/T]AACAAAATTAATTTT | 5336 |
| rs188610105 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827408 | TTCCCAGGCTGATCT[C/G]GAACTCCTAGGCTCA | 5336 |
| rs188617619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906943 | CTCAGGAGGCTGAGG[C/G]AGGAGAATTACTTGA | 5336 |
| rs188636236 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882927 | CCCTCATCTCTTGCT[A/G]CACTGTATCCCATAT | 5336 |
| rs188636412 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894390 | GCTGTGATTGTGCCA[C/T]TGCACTCTAGCCTGG | 5336 |
| rs188639286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825225 | ATGCTTATTTGGGAG[G/T]GTGTTTTTTTCCTAT | 5336 |
| rs188641980 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778595 | GAAAACGGGACATCA[A/G]TTGTCTGGGGTTCTT | 5336 |
| rs188650028 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873409 | CTTGAGAACAATGAC[A/G/T]TGTGTCATTGAACAT | 5336 |
| rs188650402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791026 | CACTGGGTAAAATAG[A/G]GTTTTGCTCTGAACC | 5336 |
| rs188650492 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802329 | GTGTTAGCCAGGATG[G/T]TCTCGATCTCCTGAC | 5336 |
| rs188657342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857909 | CAATATAGGAAAAAC[A/G]CTTAGAACAATGTCT | 5336 |
| rs188663191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845640 | TTCCCAGCCTCGGGT[C/T]AGAAAGGTGGCTTGA | 5336 |
| rs188674439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830820 | ATGGGAAGGGTGAGG[A/G]GGGCATCGGGCTTCT | 5336 |
| rs188685162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949642 | AAAACTTTTAGATAG[A/G]GAGGTGAAGAGAGGG | 5336 |
| rs188732593 | snp | A/G | 0.000677763 | 0.0183962 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934559 | CCAAGAACATGCCCT[A/G]TAACTCCAATGAAAA | 5336 |
| rs188766615 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884121 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACTTGA | 5336 |
| rs188775660 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911892 | AACCTTTGCCTCCTG[A/G]GTTCAAGTGATTCTC | 5336 |
| rs188776975 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859904 | ATTCAGTTTACTTGA[C/G]TTTTTCACTTAAAAG | 5336 |
| rs188784235 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871339 | TTTCTTCTTTTTACA[C/T]GTTTGTTTGTTTGTT | 5336 |
| rs188788950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886004 | GTTAGGTCTGAGCTG[G/T]TGCTAGAGTGAGGTA | 5336 |
| rs188805669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844761 | AGAATTTGCATAGTG[A/G]TGGACACTTGTATAT | 5336 |
| rs188809334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863621 | TATCCAGAAGCTGAA[C/T]TGCTGGATTTATTTT | 5336 |
| rs188813185 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841184 | CAGGCCCACCCCCTA[C/T]CTGCAGGCCAAAAAG | 5336 |
| rs188847492 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781820 | AAGAGACAAAAACTT[C/T]CTTGATTTCTGGTTT | 5336 |
| rs188849919 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800622 | GTCTATTGTTGATGG[A/G]CATTTGGGTTGATTC | 5336 |
| rs188860727 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955994 | GTTGTACAGTCATGG[C/T]CACAATCAATTTTAG | 5336 |
| rs188862346 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803720 | ACAGTCTCACTGTGT[C/T]GGTCAGGCCGGAGGG | 5336 |
| rs188867153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935582 | CCTCAGTTAACTTAC[C/T]GGGAGGCCAGTCCCT | 5336 |
| rs188871481 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944807 | ATCAGGGACTTGAGC[A/C]TCCAAGGATTTTGGT | 5336 |
| rs188874845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824749 | GATGTCACCTTTCAT[G/T]GGATGGTGACTCCCT | 5336 |
| rs188878090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910978 | GCCCCGAGACTTTGG[A/G]CTTTGATTTTCAGAG | 5336 |
| rs188878986 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781958 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 5336 |
| rs188884341 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891689 | GAGCCCTGTTGTGAA[C/G]CAGGTGGAGGGTGTA | 5336 |
| rs188887234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897427 | GTGCACCTCACAGGG[C/T]GGTTGTGATGATTAA | 5336 |
| rs188890977 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792933 | TCTGTGCCTCAGTTT[C/T]CATATCTGTCAAGTG | 5336 |
| rs188893453 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869968 | AGTTGGAGGACTCCA[A/T]TGCCCATTTTCAATA | 5336 |
| rs188898766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804009 | TGTGAATAATACTGC[A/G]GTGGACATTCATGTA | 5336 |
| rs188901598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854997 | GGCAGATCACTTGAG[A/G]TCAGGAGTTTGAGAC | 5336 |
| rs188976295 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961830 | AGCTATTTATAATGA[A/G]AAATTTTAGATGTCA | 5336 |
| rs188999521 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893996 | GACGGAGTCCCTGTC[A/T]TCTGTATCTCCTCAG | 5336 |
| rs189007316 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921704 | TTACTTTCAGCCCTC[A/G]GCTCCTCCTTGCCAT | 5336 |
| rs189020856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872033 | TGCTATTTTGTTAAA[A/T]ATCATAGAATACAGG | 5336 |
| rs189035992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877939 | CTTTTCTCTGTGTGC[C/T]TCTCTGTCTCCAAAT | 5336 |
| rs189042329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845095 | CAGCACACTTGGCTA[A/G]CTGCGTTTATTTTTT | 5336 |
| rs189043433 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896572 | AACAGAGCGAGACCC[C/T]GTCTCAAAGGAAAAA | 5336 |
| rs189051506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875056 | GCAACCTCTTCCTTC[C/T]GGGTTCAAGCGATTC | 5336 |
| rs189052340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865010 | ACGCAGGTTTGTGTG[C/T]AGGAGGCTTACTAGG | 5336 |
| rs189058592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851089 | CTTTCTCTCACCTTC[A/G]TCCCTAATACTCTAC | 5336 |
| rs189065773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820603 | CAGTTTTCCCCTCTG[C/T]ATAATGGGGAAACAT | 5336 |
| rs189066367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839343 | CCAAAACTGGTCAAT[C/G]CATGTGTGAGGAAAA | 5336 |
| rs189097720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943200 | TATTAGTCCGTTCTC[A/G]CACTGCTATAAAGAC | 5336 |
| rs189114648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932612 | AGTGGCCAGGTCATT[C/T]TTTTCCCCTTGGGAG | 5336 |
| rs189116472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953334 | TAGTTTTGATACTTG[C/T]ACTGTGGTTGTGCGA | 5336 |
| rs189123487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792598 | ACTCACACACAATAT[A/G]GCTGGGGAGGCCTCA | 5336 |
| rs189130404 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920556 | GGGAGAAATGTGAGC[C/G]GAAACATGGAAGATA | 5336 |
| rs189137180 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779554 | CGGGCAGGGACGGGG[C/T]GCACCCTCGGGGACC | 5336 |
| rs189137898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894604 | CCAGCTTGTCGTGGT[G/T]TCTCATGCCTGTAAT | 5336 |
| rs189139124 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796204 | GATGTCTCTTAGACA[C/G]CCTCATCTGCCCTCT | 5336 |
| rs189140652 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829259 | GATTACATGCACACA[C/T]CAACGTGCCCGGCTA | 5336 |
| rs189148713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813465 | ACTCATGATTTAGCT[C/G]TGTGTTTGTCTGTCA | 5336 |
| rs189153390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817133 | AAGACAAAGCCCTCT[C/G]TTTACAAGCGAAGTC | 5336 |
| rs189166967 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934154 | GGTGACAGAGAAGAG[A/C]CCCCTTCCATCCTGA | 5336 |
| rs189208641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945392 | GCACTATCATTTGTG[A/G]TTAAAAGCAACTCAA | 5336 |
| rs189256988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904200 | GAGGTCCTGCTTCAC[A/T]GTTGACACTTATCTT | 5336 |
| rs189261086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880122 | GGCGCATGCCTGTAG[C/T]CCTAGTTACGCAGGA | 5336 |
| rs189263732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917032 | GTATCCTTTGACCAA[C/T]ATATCCCCAACACTC | 5336 |
| rs189273749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928829 | ACTAAAACTGTAAGT[G/T]CTAAAACAAGGTCTC | 5336 |
| rs189282309 | snp | A/C/G | 0.000298213 | 0.0122074 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81854574 | GTTCGTCCTCAGCAC[A/C/G]CTCAGCTTGGCAGGT | 5336 |
| rs189285216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903600 | TGCACCCAGGCAGTT[A/G]TTTCGGAGATGCCAA | 5336 |
| rs189289161 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861755 | ACCCTCAGTGCCTCT[C/T]TCCACGCGGTGCTGG | 5336 |
| rs189295410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891242 | AAATATTTTAGGATA[A/G]ACATTACAAAGGAAA | 5336 |
| rs189295617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879676 | ATACATTTCCCTAAG[G/T]GCTTATCCAATCGCA | 5336 |
| rs189298209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882180 | ATTACCCTGGGAAGC[C/T]CCGTGTAGCAGAATG | 5336 |
| rs189301245 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848128 | TGATGTTGGCAGAAG[A/C]ATAGAAAGATTAGTA | 5336 |
| rs189301790 | snp | C/T | 0.0012083 | 0.0245497 | missense | PLCG2 | GRCh38.p7 | 16:81786066 | CCCTGGAGCTGGGGA[C/T]GGTGATGACTGTGTT | 5336 |
| rs189307895 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836218 | AATCCCTGCATTTCT[C/G]AGAGGGGGAAACTGA | 5336 |
| rs189310206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839724 | ATTACCAGCAGGAGG[C/G]TGAAAAACACCAAGT | 5336 |
| rs189314053 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857356 | ATCCCTGGAGTCAGT[A/G]TGCTGCCAGGGTAAG | 5336 |
| rs189318873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796478 | TGGTCTCCTGTAAGA[A/G]GACATCGTCTGGCTC | 5336 |
| rs189323331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807058 | TGAGTCGTCCATTCT[A/G]CCTTCTCGCCAAGGC | 5336 |
| rs189333257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817434 | AGGAGTTTCGCTTTT[A/G]TTGCGCACGCTGGAG | 5336 |
| rs189338665 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828168 | ACCTGACAAAACACT[C/G]CTGTACCCTGATGCA | 5336 |
| rs189350956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956153 | AATGGCATCGTGTGA[C/T]TTGTGATCTTTTAGA | 5336 |
| rs189418477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785747 | CAGGGGCTCTTCTCA[C/T]ACTTCAGTTTCCATT | 5336 |
| rs189427453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806625 | GCAGACATGTGATTC[A/G]TGTCTTGTAAGTTGT | 5336 |
| rs189440451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809783 | GAGGGAGTGTCTGAT[A/G]TCCCAGTTATTGCTG | 5336 |
| rs189447329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827920 | ACATGGAGAAACCCC[G/T]TCTCTACTAAAAATA | 5336 |
| rs189462172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956495 | GACCAAGCACTTTTT[A/G]AACTGCTTGCTTCCC | 5336 |
| rs189484841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935929 | AAAAAAAGTAAATTA[C/T]AGTAATTCTAGCCTA | 5336 |
| rs189485601 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914455 | TCACTTCAATGGGAC[C/T]GCGTGAATGAAGAGG | 5336 |
| rs189489907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953022 | TGAGACGCTGAGAAG[A/G]GTACATTGCTTCTGT | 5336 |
| rs189500668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938402 | GGGGAAGAAGCATAC[A/G]TAAACACAGGCCTTT | 5336 |
| rs189501865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888514 | AGCACTTTCTGTGCA[C/T]CAGGTGCTGCATTAG | 5336 |
| rs189508381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932530 | ATTAAAGCCTTCCTG[A/G]GGCCTCTTGTGCCCT | 5336 |
| rs189512935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914289 | ATGGTCAGGATGCCA[C/T]CTGTATGTGCATGCT | 5336 |
| rs189515421 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926524 | TTTAGCTGAATAATA[A/G]TAAGAGCTAACACTA | 5336 |
| rs189526074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917744 | TTTTATTTTTTGAGA[G/T]GGAGTCTTGCTCTGT | 5336 |
| rs189534713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891368 | GCCTGTTGATTTCCC[A/G]CATCAGAGCTGTTCT | 5336 |
| rs189541967 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858722 | AATTTTCCACCTATC[A/C]CTCCCTCCTGGGTTG | 5336 |
| rs189546662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846179 | AGAAATCTGCATCAC[C/G]TAGGAGGTTGTAGTG | 5336 |
| rs189555265 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831756 | AGGCTCCCCGCTCTT[G/T]CCCCAATCCTGCCTT | 5336 |
| rs189558007 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798523 | AAGTTCTGGAAATAG[A/T]AACAGTGATGATACC | 5336 |
| rs189561944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868810 | CTCCATGACCATTCC[C/T]GAAGGGTGGAGACCA | 5336 |
| rs189572478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809065 | GTTCTGAGTAGCTCA[C/T]GAGAGAGTGGGAACC | 5336 |
| rs189576306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843309 | CAAGTTGGTGGAAAT[C/G]TTTTGGTACCCTTTC | 5336 |
| rs189578915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820280 | CATCGCAGGAGAGAG[C/G]GTTCCCTCACTTCCC | 5336 |
| rs189662671 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785183 | GTTTTGGGCCCAAGC[A/C/G]CCTCTCTGACACTGA | 5336 |
| rs189710322 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81786817 | CAAATATTTGCTCTA[A/C]TTTGTGTTTTTAAAT | 5336 |
| rs189719303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820829 | TCTCATCATGTTGGC[C/T]AGGCTAGTCTAGAAC | 5336 |
| rs189720077 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823086 | GCCGTAGGGCACTTA[C/T]AAAGCAGGCGAGGCC | 5336 |
| rs189723004 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874964 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTAT | 5336 |
| rs189749387 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940487 | AATCTCGAGGGTCCA[A/G]CTCCCCAAACCCTTC | 5336 |
| rs189750961 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942978 | TGGGACTTGGGCAGC[G/T]AGAGAAGGTACATAG | 5336 |
| rs189755315 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962075 | CTCCGTCGAAGAGGA[C/T]GACCAACCCCGATAG | 5336 |
| rs189765511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898788 | TTTCCTGAGGTGATA[C/T]GGTGTGGTGATGTCA | 5336 |
| rs189769698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911388 | CACGTGGCAATAACT[G/T]TGCCTCCCTGGGAGC | 5336 |
| rs189770739 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918019 | TGAGCCACCACGCCC[A/G]GCCTTTGTCCATTTT | 5336 |
| rs189771347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920272 | TTACTTTGTCTCCAT[G/T]CCTACCACATAGATC | 5336 |
| rs189783295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901928 | TTATTCTGAGAAAAG[A/G]GTCTGTAGCTTTCCC | 5336 |
| rs189786048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885239 | ATGTTGGTCAGCCTG[C/G]TCTTGAACTCCTGGC | 5336 |
| rs189790370 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877051 | TTATTTTACTACCTG[A/T]TGGGATCAGCAGGAG | 5336 |
| rs189792137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844195 | GAGACGAGGTTTCAC[A/G]TGTTAGCCAGGATGG | 5336 |
| rs189796556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862304 | GCTGTTTCATTTTTT[C/G]ACTTTTCTAGAGGCA | 5336 |
| rs189805134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848344 | CAGATGCCTGCAGCT[C/G]TTTCCTGGGGCAGGG | 5336 |
| rs189826484 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962964 | TTAGTGTTGGAAGGA[A/G]CGAGGACCTTATAGT | 5336 |
| rs189833111 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875755 | AAAATAGAAAGCACT[A/T]GCAAAAAATCAAAAA | 5336 |
| rs189845088 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847512 | TCCTGAGGTATCTAG[A/G]AGCCCCCAGCCCTAC | 5336 |
| rs189858822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950738 | GAAGATAATAATTTT[C/G]TAAATATACTAAAAC | 5336 |
| rs189868947 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941781 | GGCTCACTGTAACCT[C/G]TGCCTCAGCCTCCTC | 5336 |
| rs189954220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788300 | TATATATATTTTAAT[A/T]GACAGAGTCTCGCTC | 5336 |
| rs189955437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813989 | ACCAGAGATGGAGAC[C/T]ATGGTATTCAGGGGC | 5336 |
| rs189967758 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798763 | AAGGCATGGTGAGAG[C/T]ATGTGCAGCAGGAAG | 5336 |
| rs190001915 | snp | C/G | 4.97409e-05 | 0.00498678 | missense | PLCG2 | GRCh38.p7 | 16:81921222 | ATAAACTCCCTCTAC[C/G]ACGTCAGCAGAATGT | 5336 |
| rs190018483 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950404 | GCAAATAGCATAGTA[C/G]CTAAGTATATAAGAC | 5336 |
| rs190020281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908881 | AAAGACAAGATCTGA[C/T]CCTACTCTTAGATGA | 5336 |
| rs190027235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929563 | ACCGTGCCTGGCTAA[A/T]TTTTGTATTTTTAGT | 5336 |
| rs190029688 | snp | C/T | 0.000630339 | 0.0177418 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895773 | CTGTCAGTGAACACA[C/T]GTGGTATTGAGGCTG | 5336 |
| rs190031162 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883747 | GATGGGATCAGATTC[A/G/T]TCAAGCCTGCCAGGT | 5336 |
| rs190033759 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904571 | ATCCCCATTGGGTCC[C/T]CCGCCACCCTGCCCA | 5336 |
| rs190034917 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874588 | CTGTTTTGTGATTTG[C/G]GGGGAATGAGGGCCT | 5336 |
| rs190046451 | snp | C/T | 1.66446e-05 | 0.00288479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859191 | CAGTTTTTTTCTGAT[C/T]ACTTTGGATTTCGAT | 5336 |
| rs190053208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947181 | CAGCAGAGAAAATTA[A/G]TATATTTAAAAGAAA | 5336 |
| rs190057744 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926466 | TTCATAGATGGATTA[C/T]GTCCCGTGTTGTTAG | 5336 |
| rs190063189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832426 | ACACGATCTCACTCT[A/G]TCACCCAGGTGGGAG | 5336 |
| rs190069872 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884491 | TCTTACCAGCTGCAC[A/G]GCCACCGACAGGTGG | 5336 |
| rs190074446 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883048 | GTAGACACCAGGGCC[C/T]GCCCCTTGAGATTCC | 5336 |
| rs190078954 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960930 | GCCTGAGAAAATGCC[C/G]TTTTCTCACCTTACA | 5336 |
| rs190083828 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900419 | ATCAGATCGCAGCTG[C/T]TCTGAGTCCCAAGAC | 5336 |
| rs190085894 | snp | A/C | 1.65649e-05 | 0.00287788 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858219 | GTAAGCAGACGTCTT[A/C]CCAGGAATTAACACA | 5336 |
| rs190093235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860752 | GAGGCAGGCAGATTG[C/T]CTGAGCTCAGGAGTT | 5336 |
| rs190104216 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831200 | CAAGTGTAATAAATA[C/T]TGACTTGTCTCTGTC | 5336 |
| rs190106939 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835572 | CGACAGAGCAAGACT[C/T]GGTCTCAAATATAAT | 5336 |
| rs190112093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949131 | CACCATGAGATGGAA[A/C]GAAAGGAAAAGGTGG | 5336 |
| rs190130431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805231 | AAGGCCAGGCTCGGT[A/G]GCTCATGCCTGTAAT | 5336 |
| rs190135183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815455 | ACTGCAGGGGCTGAG[A/G]GACCACCCCCTAGAG | 5336 |
| rs190209848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790332 | CGTGATTGGATTTGC[A/G]TCTTTGAGCATGCAG | 5336 |
| rs190216072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788130 | CAGTTTCATCATTTT[A/T]GGAACTGTCAGACTG | 5336 |
| rs190226601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809449 | CACAGGAATAATAAG[C/T]TTGATGACACAGCCT | 5336 |
| rs190237755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945655 | TGACTGTGAAAGACA[A/G]GTCCTAATTGTAAAG | 5336 |
| rs190251941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957519 | ATGGGCTAGTCCAGC[A/G]GCTCTAGACTGGGTC | 5336 |
| rs190262183 | snp | A/T | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936377 | CAATTTCCAGACGGC[A/T]GGTAAAGGCCGACTG | 5336 |
| rs190272688 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958755 | CCAGCTGCTGGGAGG[C/G]TCTGGCCCCACTAGT | 5336 |
| rs190272791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911547 | GGCTCAAGTGATCCT[C/T]CCACCTCAGCCTCCT | 5336 |
| rs190275260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925005 | GTCAACATCCTGGTG[C/T]GCACTGGGTGGGTGA | 5336 |
| rs190308032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935862 | CCATTCTCCCTCTTC[C/T]ATAACTGTACCACTT | 5336 |
| rs190313919 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911150 | GAAGGGTCAACAAAT[G/T]CTGGGAATAAAGAAA | 5336 |
| rs190323307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913167 | CTAGGCCTGTGGTTC[C/T]CTAATGTTACCCCAA | 5336 |
| rs190327459 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887410 | AGGCATGAGCCACCA[C/G]GCCCGGCCTAGTATT | 5336 |
| rs190330757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884808 | TTGCAGAACATTTCA[A/G]ACATACACAAAAGCA | 5336 |
| rs190331116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873922 | GCTCTTATTAAGGCT[A/T]GTCTGTGTGTTTGTG | 5336 |
| rs190343102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845893 | CTTGACTATGAGTCA[A/G]AGTTCAAATGCTGGC | 5336 |
| rs190369734 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781048 | ACAAACAAACAAACA[A/C]ACACACACAAACACT | 5336 |
| rs190383917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842685 | CAGGGGTGGGAGGAC[A/G]TTCCGTGGGTGCAGG | 5336 |
| rs190385278 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817920 | TTTCGGGGAGAAGGG[G/T]GTTAAGTGAACACTT | 5336 |
| rs190385458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791711 | CTGGGATTACAGGTG[C/G]GTACCATCACATGCA | 5336 |
| rs190390227 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802696 | CATGCCTCAGCCTCC[C/G]AAGTAGCTGGGATTA | 5336 |
| rs190396476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828597 | CTTTGCTTTTATGAG[C/G]TGCAGTTTTGATCAG | 5336 |
| rs190400904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813049 | ATATCTATTTTGGTA[C/T]CAGTACCATGCTGTT | 5336 |
| rs190439718 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778216 | CCTCATGTCGAAAAA[A/T]GAGAAAATTAGCCAA | 5336 |
| rs190460248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801691 | TTTTCTTTAATTTTT[A/T]TTTTCTTGAGGTGGT | 5336 |
| rs190476724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955151 | TGCTTACTCTTCAAC[C/G]TTTGCAAACAGCTGG | 5336 |
| rs190480054 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843675 | CAGTAATGTTTCTGA[A/G]TTAGGATATTCTTCT | 5336 |
| rs190484517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822885 | GAGGCCACACGGCCA[C/T]GATTGCAGGCGGCCA | 5336 |
| rs190485229 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943984 | TGGGCTCATTTTGAA[G/T]AGAACAAAAGAGGAC | 5336 |
| rs190496363 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783068 | AGGTTAAGTCCAAGG[A/C]CCTCCCAGAGTGAGG | 5336 |
| rs190505884 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933956 | CCCCTTGGACAGAGC[C/G]CTGATGGGCAGTCAG | 5336 |
| rs190510549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804633 | TTTGTCCAAATGTTG[C/T]GGTGAAGCATAGCAC | 5336 |
| rs190516345 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909284 | GACATCCCTCCCTTT[A/T]TTGGGGGGGTTTAAT | 5336 |
| rs190525502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826045 | ATCTAGTAAATATTT[A/C]AAACTCAACGTGTCC | 5336 |
| rs190537581 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959092 | TAATGTAATATGGCT[C/T]TTTAAAGGAGAGGAG | 5336 |
| rs190549467 | snp | C/G | 4.67738e-05 | 0.00483577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923627 | CTGGGCTGCTCGGCA[C/G]GTGGGCTTGACTTGT | 5336 |
| rs190555559 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944922 | ATACAAGTAATCCTT[C/G]TAATTTTTTTTAGTG | 5336 |
| rs190582054 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898327 | AAAATGATTGCAAGC[A/C]GCGTTCATTCGAATG | 5336 |
| rs190591877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852760 | ACAATCTGGGCATGG[A/G]TGGGGACTGGGAGAG | 5336 |
| rs190592047 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874160 | ACATTTAAAACTTGA[C/G]AGATTATATTATATA | 5336 |
| rs190594704 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876020 | TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 5336 |
| rs190620635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783568 | TTTTGATCTTTGTGC[G/T]GCTGCTGGTCTACAT | 5336 |
| rs190625097 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793718 | GCCTCTTCTAATGAA[C/T]GCTCACTGTGTCCTA | 5336 |
| rs190630607 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854238 | ACTCCAGGGGTTTGT[G/T]GGGTGGCAGCAAATG | 5336 |
| rs190642017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804995 | GTCTGTGAGTTTTGC[C/T]TGGTTTACTCCTAAG | 5336 |
| rs190649952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814856 | CAGTGGGGATTATGA[C/T]GATCCTCTCCCCATA | 5336 |
| rs190687540 | snp | A/C/T | 5.65519e-05 | 0.00531727 | missense, synonymous-codon | PLCG2 | GRCh38.p7 | 16:81889258 | AACTGCTGAGCCTTT[A/C/T]TTGTTTGTGGATGAG | 5336 |
| rs190700518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878809 | GTCTTCCTTATCTTG[A/C]CTCTCACTGTTGGTT | 5336 |
| rs190706910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867297 | TCTTGACCACTCTGT[C/T]TCAGCTCTGCTGGAC | 5336 |
| rs190716998 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851696 | TTTTGTATTCTTACT[A/T]GAGATGGGGTTTCAC | 5336 |
| rs190728614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841025 | ATGAATATGAAGCAT[A/T]AGAATCACAGACCTA | 5336 |
| rs190753449 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793454 | CACCTGTTTGTGGGT[C/G]TGGAATTTTAGGGTC | 5336 |
| rs190765464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814671 | CTGCACTCCAGCCTG[C/G]GCAACAGTACGAGAC | 5336 |
| rs190775158 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787156 | CTCCAGAGAAGGGCA[A/T]TTCATGCTATTTCCA | 5336 |
| rs190777263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797000 | ATACTATGGATGGGT[A/T]GTGGTTTGTCATAAC | 5336 |
| rs190785536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808562 | GCGGTGGCATGATCT[C/T]GGCTCGCTACAACCT | 5336 |
| rs190794404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947753 | TCCTTTACTTTGCTA[A/G]CAGTATGTTTGTTTA | 5336 |
| rs190797124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818965 | TTTAGTGAGAACTTA[C/G]GGTATTTCCAACACT | 5336 |
| rs190798874 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930100 | CAGCTACTCAGGAGG[C/G]TGAGGTGGGTGGATC | 5336 |
| rs190804097 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818544 | TGCACGGAAATGGAG[C/G]TCCGAAGGCCTGAGC | 5336 |
| rs190832444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881214 | GGGCCTCCTTTCCCC[A/G]AATGTGCCTCATGAG | 5336 |
| rs190840748 | snp | A/C/G/T | 0.000182523 | 0.00955163 | missense | PLCG2 | GRCh38.p7 | 16:81883327 | TTCCAGAGGTTTCTC[A/C/G/T]TACATGAACAGCAGG | 5336 |
| rs190846990 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841387 | ACAGGCACCCAGGCG[C/T]TTACTACCATGCCCA | 5336 |
| rs190848358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855857 | GGATGTAGGAAATGA[A/G]GAGCGAATGTCTGAC | 5336 |
| rs190883021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836734 | AACAGAGCAACACTA[C/T]GTCTCAAAAACGAGT | 5336 |
| rs190895881 | snp | A/C | 0.00517822 | 0.0506191 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962748 | TATATTCCCAAATAA[A/C]ACACACACACACATA | 5336 |
| rs190910518 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940924 | CTTCCTCTTCCTTTA[A/G]TATTTCTGATGCATG | 5336 |
| rs190930715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950561 | TTGTGTCCTACAAAT[A/G]GATAACATACACTAT | 5336 |
| rs190942235 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918474 | AATTTTTTTAAATCT[A/C]GGTTTCCCAACCCTA | 5336 |
| rs190948132 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877378 | GGAGAATGGCGTGAA[A/C]CTGGAGGCGGAACTT | 5336 |
| rs190955157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904894 | GCTATTTTTACTTAT[C/T]TATTTTTTACTGGGA | 5336 |
| rs190962362 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863708 | GTTTCTGTTTTCTTC[A/G]TATCCTCACCAACAC | 5336 |
| rs190965346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891738 | TAAAATACACAGAAG[C/T]TTCTGGAAGGGGCTG | 5336 |
| rs190968550 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81880348 | ATCAAAGCCAATGTG[C/G]CTACAATGTGCTGTG | 5336 |
| rs190971704 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850057 | GTCAAAGGCACAAGA[A/G]AAAACAAAAGTAAAC | 5336 |
| rs190979349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837947 | GTACTTGTGTGTATT[A/T]AGTTATGTACAATTT | 5336 |
| rs191014103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789094 | TAACAAACCTGCATG[C/G]TCTTCACATGTATCC | 5336 |
| rs191020056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800381 | TTACCCTGCTCCCCA[A/G]CAGGCCCTGGTGTGT | 5336 |
| rs191032169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809949 | CTTTCCCATGCTCTC[C/T]TCATCTTTCTGCCAG | 5336 |
| rs191038677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954698 | GGCTGCATAGTATTC[C/T]ATGGTGTATATGTAC | 5336 |
| rs191041968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821901 | CAGAGCAGCACAAAG[A/G]GAGAGCCAGACAGGC | 5336 |
| rs191043556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808173 | GAGTGGAATTGCTGG[A/G]CCATGCAGTAACCAT | 5336 |
| rs191053631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794223 | GGTGCCGAAGTGAGA[A/G]TTTACTGTATTTTGG | 5336 |
| rs191057950 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933553 | AGCTGCAGGCCTGGA[A/C/G]AGTAATTGTCATGCT | 5336 |
| rs191059474 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828913 | AGAGGCTGTATCTTA[C/T]CAACTGCATTCTGAT | 5336 |
| rs191066001 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918836 | AAAACCAAGGAGGCT[C/G/T]TTCTGTTTTGGATTT | 5336 |
| rs191067922 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892226 | GGAGGAAGGCAGGTC[C/G]TGCTGGAGCAGGATC | 5336 |
| rs191095368 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871007 | AAGTCTGGCATGTTC[C/G]TAAGAAACCCACAAG | 5336 |
| rs191154757 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840068 | TCTCCAAAAAAACTT[A/C/G]AAGAATTATTTGATG | 5336 |
| rs191169197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953857 | GGAAAGGTGATAAAG[A/G]GTTGCAGTTATAGAA | 5336 |
| rs191179913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939149 | TCAAGTCCGGAATCG[C/T]AGGTGAGGCCCTGAC | 5336 |
| rs191180071 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948684 | AAGATTTCCTTACAC[A/C]TGGGGAGACCTGGAG | 5336 |
| rs191184843 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915642 | CGACAGCTTACCCTG[A/G]ATAAGCTAATAGACG | 5336 |
| rs191194754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927521 | TTGGACAGCCAGACA[C/T]TGAGAACGTGCTTGG | 5336 |
| rs191204163 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902551 | GCCTCTTTTATAAGG[C/G]CACCATTCCCATTGT | 5336 |
| rs191209940 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878970 | ACAAGCAGAGTGTCC[A/G/T]GGCAGGGAGTTGCAA | 5336 |
| rs191211926 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890118 | AACGCCCGAAAAGAC[A/G]TCTCAAAAGGCCAAT | 5336 |
| rs191284014 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799718 | CTGCCTCAACCTCCC[A/G]AGTAGCTGGGACTAC | 5336 |
| rs191292581 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784368 | GTAGCTTTTTGTCTT[C/T]CCAGCTGCCCCTTGT | 5336 |
| rs191299004 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786507 | GTTCCCACAACTGGT[C/T]GAGTCATCTTTCCTC | 5336 |
| rs191314045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943753 | AAGGCAAAAAACAAA[C/G]TAGCAACAAAAATCA | 5336 |
| rs191315533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807766 | TCAGCATGGCTGGAG[A/G]GGCCCCAGGAAGCTT | 5336 |
| rs191323463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919415 | TTGTATCTAATCAGT[A/C]GGGTTTGTGTAAAAA | 5336 |
| rs191325926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942198 | TTGAAGGATGAGGGC[C/G]TTGAGCCTCATAACC | 5336 |
| rs191350079 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824373 | TCCTGATCTTAAGTA[A/T]TCCACCCACCTCAAC | 5336 |
| rs191369457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899408 | GAAGGATACAGGTGA[C/T]CCTTATTGGTGGATT | 5336 |
| rs191370516 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878534 | CTGTCAACTACAGCC[C/T]CATTTATCTGCCCCC | 5336 |
| rs191379646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877230 | GAGGCCAAGGCGGGC[A/G]GATCGCGAGGTCAGG | 5336 |
| rs191388400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851547 | AGGCGAAGTCTCACT[C/G]TGTCACCCAGGCTGG | 5336 |
| rs191397959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849101 | CTTAGGCCACGTGGG[G/T]TTGGAGGGGTCATCA | 5336 |
| rs191420202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937095 | CTTGCATTTTGATCA[A/T]CTTTGCCCTGAGGAA | 5336 |
| rs191426569 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946052 | CAAAGTCAGCCCCCA[C/G]CATGGGGCACTGACT | 5336 |
| rs191431107 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912520 | GTCACTGGTGCCATT[A/G]TCTTGTCCTCTGCGG | 5336 |
| rs191435085 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925845 | TGAGCTGAGATCGTG[C/G]CATGCACTCCAGCCT | 5336 |
| rs191443145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899856 | TAAACAGAAACACAC[A/G]TAAAACAACGTCAGA | 5336 |
| rs191455369 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803256 | CCTGAGTAGCTGGGA[C/G]TACAGGTGCCCACCA | 5336 |
| rs191461098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787501 | CCAAAGCATTGGGAT[G/T]ACAGGCATGAGCCAC | 5336 |
| rs191461243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857429 | AGTGTGCTCTGGCTA[C/T]TGTAATGAAATGCTG | 5336 |
| rs191463326 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886539 | GCAGCATTTTTAATA[A/G]GAATGAAAACTTGGA | 5336 |
| rs191467247 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813381 | CTCTTTGAAGAGGTC[A/C]TTCACATCCCTTGTA | 5336 |
| rs191469358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845132 | TTTTTTAGAGATGGG[A/G]TATTGCTTTGTTGCC | 5336 |
| rs191471158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877516 | TGGAGGTTAAAAGTC[C/T]AAAATCCAGGTGTTG | 5336 |
| rs191471467 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864590 | AAAATAATAGTTCCC[A/G]CCTCCCAGGGCAGAT | 5336 |
| rs191473313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824559 | GATCATGTTTGGATC[C/T]CCCTCAGGCCTTCTC | 5336 |
| rs191475395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797657 | TGCCCCTTTCAGCCT[C/T]GGACTTCCGGTTTCT | 5336 |
| rs191477281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830041 | ATATATAATAGTGGC[C/T]GGGTGCAGTGGCTCA | 5336 |
| rs191529649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951299 | CTTTGCCTACTTAAT[A/T]AAAGAATAAAGAGGA | 5336 |
| rs191552390 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796554 | CTTACCAATTTCATA[C/T]GTCAAGGTCCTAATC | 5336 |
| rs191569028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930577 | AACATGGCGAAACCC[C/T]TCTCTACAAAAAATA | 5336 |
| rs191579935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948420 | AACTGGCTGCCCCAC[A/G]ACCTGTTTAGTACTG | 5336 |
| rs191592935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800650 | TTCCCTATCTTCGCT[A/G]TTGTGATACTATTGC | 5336 |
| rs191606821 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817008 | TTGCCCAGAAGGTGA[C/T]GGGCACTGGATGCGT | 5336 |
| rs191611388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841875 | GCAGGGTCCTTGGCT[A/G]AGATCAGTAAGCAAC | 5336 |
| rs191613594 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927347 | AATTGAGATTGAGTT[G/T]TTGTGGGTGAGTTGC | 5336 |
| rs191616853 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885923 | GCTTATTTGCCCAAC[C/G/T]TGAGACTAAGTTTGA | 5336 |
| rs191617341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822145 | TAGAGCTTGTTATCA[A/G]TTTCTCTTAGCTTTG | 5336 |
| rs191618629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827603 | GCAGGTTGTATCTAG[G/T]GGACAAATGACAATA | 5336 |
| rs191619253 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884047 | GGCAGCCCCCCCTAC[C/T]CCCCAGCGAAGAAGT | 5336 |
| rs191621653 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902277 | TGTTTCCTAGGTATT[G/T]CAGTCTGTTCCTGCA | 5336 |
| rs191637645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863295 | TATAAGTGGACTAGC[A/G]GAATATTTGTCCTTT | 5336 |
| rs191644710 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935325 | CCAGAATAAGCCTCC[C/T]ATTTCAAGCTCCTTA | 5336 |
| rs191655166 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837887 | CATTCACAACATTCA[A/C/T]AGAACCCACTACCAG | 5336 |
| rs191659525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922458 | CGATACTATAGTTAG[C/T]ACTTAAGAAGTGCAA | 5336 |
| rs191667651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897114 | GGCTGTGTTCCAGTT[A/G]AAACTTGAATTACAC | 5336 |
| rs191668546 | snp | C/T | 0.000513419 | 0.0160139 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910598 | CTACTTGACTGACAA[C/T]CTCACCTTCAGCAGC | 5336 |
| rs191672786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939520 | GGGCTCTCCCCTGCC[A/G]GCTGTAGAACCCCCT | 5336 |
| rs191681809 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884344 | CAACAGAGCAAGACT[C/G/T]CGTCTCAGAAAACAA | 5336 |
| rs191683326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875342 | TATTGCCATTTTAGG[A/G]ATTAAGAAACTGAGG | 5336 |
| rs191687802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801260 | AATAAAATATAGTTA[A/G]GTTCTCATAAGTACC | 5336 |
| rs191688843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860386 | TGTAAACTCATTTGA[A/G]GGAGCTGTGAGTGGG | 5336 |
| rs191839304 | snp | A/C/G/T | 0.00125293 | 0.0250032 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905528 | CCTTGGTCCCTTCCC[A/C/G/T]TAGCCACTGCGGCCA | 5336 |
| rs191844142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791558 | GAAGACTGAGCTTAG[C/G]TGGGATTATTTTTTG | 5336 |
| rs191847325 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936694 | GTTCTCTTCTCCAGG[C/T]CTGTTGCTGTGTGAG | 5336 |
| rs191852539 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958648 | TTACTGGGATGGAGG[A/G]TAGGAATCTTGGGGC | 5336 |
| rs191852855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781994 | CTCCTGCCTCAGCCT[C/T]ACGAGTAGCTGGGAT | 5336 |
| rs191855045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957844 | ACACTCAGCCCTATA[C/T]CATCCAGCTATGAAT | 5336 |
| rs191855624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881705 | GCTGGAGTGCACTGG[C/T]GCAATCTTGGCTCAC | 5336 |
| rs191856941 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893251 | GTTTTGGTGGATATG[G/T]CTCCTAGCATAGCCG | 5336 |
| rs191858877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792966 | ATAATAGTAGTTTCT[A/G]TCTTATTGGGTGAGA | 5336 |
| rs191863851 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812576 | TCTTTGTAGATTCTG[C/G]ATATTAGCCATTTGT | 5336 |
| rs191869463 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871237 | AAAGTGCAACTCACT[C/G]TACTGCATTATTTCA | 5336 |
| rs191871461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829513 | GTGAGCCACCACACC[C/T]GGCCCATTTCTCTGT | 5336 |
| rs191871618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804196 | GCTCCAACTTCCCCA[C/T]GTCCTCGCCAACACA | 5336 |
| rs191872959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856410 | TATGATCTTCCTTTT[G/T]CCAGATGCCAAGCTC | 5336 |
| rs191874835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926293 | GAGGCCCTGGGGAGC[C/T]ATCATGTGGTGTGGT | 5336 |
| rs191877491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814107 | AGAGAGGATAAGGGG[A/C]TGGGAACCCAGGCTG | 5336 |
| rs191878393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946584 | TAGATAGACTCATCC[C/T]TTCTGGATGCTTTTT | 5336 |
| rs191878919 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912015 | TGTTAGCCAGGATGA[C/T]CTCGATCTCCTGACC | 5336 |
| rs191879992 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937514 | CTACATAGACACTTT[C/T]AGCAAGTTTGAATCT | 5336 |
| rs191882772 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789547 | TCCCACCTTGGTCTC[C/T]GAAAGTGCTGGGATT | 5336 |
| rs191883610 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825634 | AGTAATAGTAGGTTG[G/T]TGCAAATGTAATTGC | 5336 |
| rs191884330 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886037 | GAGAAATTCATGCAC[C/T]TTTTTCCCTTCATTA | 5336 |
| rs191887711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939046 | CCTCCCTCTTGCCCA[C/T]ATGGTTCAGCTTGAG | 5336 |
| rs191889179 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959927 | GCTAAGGCCTGCATC[A/C]CCTTTCTGCCCAAAT | 5336 |
| rs191891202 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826479 | GCCTCAGTCTCCTCA[C/T]TGATAAAATCGCAAT | 5336 |
| rs191898219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810072 | TCTCAGCTCACTGCA[A/G]CCTCCTCCTCCTGGG | 5336 |
| rs191903474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896529 | GTTACAGTGAGGTCA[C/T]ATTGCGCCACTGCAC | 5336 |
| rs191915879 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870379 | TTGGAGCTGAGTTCT[C/G]TCTGACTCCCAATGC | 5336 |
| rs191925656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914571 | GTCTTGAGAATGGAA[A/G]TTTTTATTTTTTAGA | 5336 |
| rs191931570 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875027 | GGAGTGCAATGGCAC[A/G]ATCTTGATTCACTGC | 5336 |
| rs192019529 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844215 | AGCCAGGATGGTCTC[A/T]ATCTCCTGACCTCGT | 5336 |
| rs192074059 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960366 | AAGACTAGTAACAGG[C/T]ACATTCTGAAAGATG | 5336 |
| rs192093172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956040 | CAAAAAGAAACCTCA[C/T]GCTCATTAGCTGCTG | 5336 |
| rs192094401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805479 | ACTTCAGCCTGGGTA[A/G]CAGAGCGAGACTCCA | 5336 |
| rs192096640 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903342 | GTCAACAGAGAAACA[C/G]CAAACAGTGCAAGGA | 5336 |
| rs192106684 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943491 | CAGTCACCTCCCACC[A/C]GGCCCCAGCTCCAAC | 5336 |
| rs192113689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826955 | GCCTCCTGTGGATCC[C/G]ATGAGATGACTGAAG | 5336 |
| rs192116095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784952 | AGGGCTCAGGGAGGG[A/T]CTAAGGGATTTTGAG | 5336 |
| rs192119847 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921122 | TAACCATAAGGAAGC[C/T]TAGAACCCTTGTTAT | 5336 |
| rs192120146 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891069 | TTGGGAGGTTGAGGC[A/T]GGAGAATCGCTTCAA | 5336 |
| rs192126454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879578 | CCATGACGTCCTGGG[C/T]TGCAAGGAGTTCAGC | 5336 |
| rs192127060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935765 | TGTGGGCTTTGGCAG[A/G]TGATTCTCAGTTTGT | 5336 |
| rs192128492 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867954 | TCCGCCCGCCTCAGC[A/C]TCCCAAAGTGCTGGG | 5336 |
| rs192129071 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944862 | CCCCATAGATATCAA[A/G]GGCCAACTGTAGAGT | 5336 |
| rs192130034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795478 | TCCTGTAAGTTTATC[A/T]CTCACTCACTCAAAT | 5336 |
| rs192134254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895229 | GTTTTCAACAGGTAA[A/C]GTCAGAAAATAAAAC | 5336 |
| rs192134422 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805970 | AGTTTTCTAGTTGCC[A/T]CATTCATAAAGGTAA | 5336 |
| rs192139816 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945840 | ACTCTTTTGGTCTCA[G/T]GAGTATTTAAGGAAT | 5336 |
| rs192142608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853849 | TCATAGTTTACCACT[C/G]TCTTCTCACAGGCCC | 5336 |
| rs192143027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816033 | TGCCACTGCACTTCA[A/G]CCTGGGTGACAGAGC | 5336 |
| rs192143951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780022 | CCAAAGAGGGCATTA[C/T]CCGCACAGCGCAAGA | 5336 |
| rs192147075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842252 | GAACTCAGCCAGGAT[A/G]CATGTGCTCAGAGAA | 5336 |
| rs192154882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827417 | TGATCTCGAACTCCT[A/G]GGCTCAAGGAGTTCA | 5336 |
| rs192158558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802590 | TTTTTGTTTTGAGAC[C/T]GAGTGGAGTTTCACT | 5336 |
| rs192166901 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925575 | TTCCCACCACCACGG[A/C]GCACAGACTTGATTA | 5336 |
| rs192172776 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824044 | CTTTCCTTTCCTTTC[A/C]TTTCCTGTCCTGTCC | 5336 |
| rs192193723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899821 | TGTCAGTCAATAATA[C/T]ATACCAAATCAGGTG | 5336 |
| rs192241685 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855385 | CCTAGAATTTATTGA[C/T]TTAGAAGTATATGTA | 5336 |
| rs192289929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952996 | AGGTTGAAATCACGT[A/G]CTTCCTGAGGTGAGA | 5336 |
| rs192299828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932311 | CCTCAGTTTCCTTGT[A/C]TGCAAAATGAGGAGC | 5336 |
| rs192312205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906270 | TGACTCCTTCGTGTC[C/G]TCCAACTGGGGGTCG | 5336 |
| rs192326514 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781384 | TATTTATCCAGGAGG[C/T]CCCCCACATTGATGA | 5336 |
| rs192330742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952381 | GACACCCCAGTCATT[G/T]GATTCTCAATTCCAG | 5336 |
| rs192337144 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882267 | TGGTGGCCTGCTGGC[C/G]AAGGCGGGAGTCCTG | 5336 |
| rs192352320 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932014 | TAAAGCAGTCTGGAT[A/C]CTCCTGACAGAAAAC | 5336 |
| rs192361136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942286 | GGCATCAAAGTGTGT[C/T]AATTCATCTGCAGAA | 5336 |
| rs192368934 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919861 | GGAGATGCAACAAAT[C/G]ACATTTAAAATATCC | 5336 |
| rs192375779 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893610 | AGAGCTTTGGCGGCT[C/T]GGGCGGAGAAGTTCC | 5336 |
| rs192378045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906004 | TTTTATTTTGAAATA[A/T]TTTTAGATTAAATAT | 5336 |
| rs192381797 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820005 | AATATCTCCCATTGA[C/G]TACCCTCCAGGGAGC | 5336 |
| rs192384024 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839013 | ATTTCCCTTTATGAC[A/T]CACAGAACCAAGCCG | 5336 |
| rs192473478 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820290 | GAGAGGGTTCCCTCA[C/T]TTCCCTCTGCAGTCT | 5336 |
| rs192482898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815918 | AATACAAAAATTAGC[A/C]AGGCATGGTGACTTG | 5336 |
| rs192482917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932683 | TTGACTCACTCAACT[C/G]TTCTGCAGGGAAGTG | 5336 |
| rs192485375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908089 | TCCAGCTGTGGTCAT[C/T]TTTCCCGCTGTTTAT | 5336 |
| rs192511820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867652 | CTATTGTTACTGCTG[C/G]TGCTGCTCCTTTTGC | 5336 |
| rs192562513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955958 | AAAGTGTACAATTCA[A/G]TGGTTTATAGCCTAT | 5336 |
| rs192586840 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949915 | AAATAAACTATACTG[A/C]AGAGGGAGATTTAAT | 5336 |
| rs192603875 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961855 | ATGTCAATATAGCAA[C/T]GTGCAAGAAGATAGA | 5336 |
| rs192605835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928955 | AAGCTGAGCTGTCAG[C/T]CTGGCTGAAATGCAG | 5336 |
| rs192606631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916255 | TCGCTTAAAGCAATA[C/T]ATTTTTTTTTTCAAA | 5336 |
| rs192614164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890769 | CCAGGAATTGTAACT[G/T]GAAATTTCCTGCCCT | 5336 |
| rs192615165 | snp | A/G/T | 0.00116848 | 0.0241447 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940100 | TCGATTTGGGCTGGC[A/G/T]TTGTACTTTGGTTTG | 5336 |
| rs192622736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917523 | ACCCACCAGGTGCAG[C/G]GGTCCCCTTTTCTCC | 5336 |
| rs192627917 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810564 | CAAGATGACACTCTG[A/C]CTTCCTGTTTTAGCT | 5336 |
| rs192631787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847444 | GTTGGGGGTAGGGCT[A/G]AAAGTTCCAACCCTC | 5336 |
| rs192635231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795710 | CCTGCTTTTTTTTTT[C/T]CTCCCCAAGAGATGG | 5336 |
| rs192639199 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903746 | TGCTCTTCCCTGTTC[C/G/T]CAGCTCATTCCTTCT | 5336 |
| rs192641943 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867807 | AATTCACGCCATTCT[C/T]CTGCCTCAGCCTCCT | 5336 |
| rs192647603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891285 | TCCATGGAACAAATA[A/T]GTCGCTGCAGCCCAT | 5336 |
| rs192661383 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790110 | CTACCCCACAGGCTC[A/G]TGGTTGGGAAGAAGC | 5336 |
| rs192674217 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875163 | GAAACGGGGTTTCAC[C/T]GTGTTGGCCAGGCTA | 5336 |
| rs192676224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859965 | GCACAAAGCTCTATG[A/G]CGGACTATTATTATT | 5336 |
| rs192680305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801453 | GTGAAGATTTTCCAT[C/G]TTGATGTAGCTTTAT | 5336 |
| rs192685844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942786 | TAATTAATTTCGAAC[C/T]CCGTGTTCCTCCTCT | 5336 |
| rs192687300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811434 | GAAGATGATGGATTC[C/T]CTAGGCTGGGAACTG | 5336 |
| rs192689260 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846906 | TATGGTTTTCCCCCC[A/G]CGCATCAAGCAAACA | 5336 |
| rs192698225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822802 | AGGCAGGAGATCAGA[A/G]TGAGTAGAAGACAAT | 5336 |
| rs192699187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833837 | ACAAGCATGAGCCAC[A/G]GCGCCCGGCCTCCTG | 5336 |
| rs192708751 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958137 | TCAAGGACATTTCTT[A/G]AGACCCAACTGGCAT | 5336 |
| rs192712909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920055 | GATAGCATGCGCAAA[A/G]GTCCTGAGGTAGAAG | 5336 |
| rs192718920 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894292 | AAATTAGCTGTGTGT[A/G]GTGGCATGCGCCTGT | 5336 |
| rs192721496 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872048 | AATCATAGAATACAG[A/G]CCAGGTGCAGTGGTT | 5336 |
| rs192722183 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792138 | ATCCCAATTTATGAT[A/G]CAAATCCCTGCTCTG | 5336 |
| rs192742782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850635 | CTCTTCCTGGCTCCC[C/T]GAAGACAGTCAGGAG | 5336 |
| rs192743723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808987 | GTTGGTGGTGTCTAC[C/T]AGGCATTGTCCTCTA | 5336 |
| rs192749698 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803667 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 5336 |
| rs192751009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829805 | GTGCTGAGTCCCTTT[C/G]TCCTTTGAAATTGCA | 5336 |
| rs192778201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900280 | TTGTGCTGTCTGTTC[A/C]TCTTTTCTGTAGGTT | 5336 |
| rs192779915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787224 | CTTTTTTTTTTAAAA[C/G]AAAATTAATTTTTTT | 5336 |
| rs192784402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877659 | CTGGCTGCTGGTGGC[G/T]GCCAGCAGTCCTACA | 5336 |
| rs192791197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808825 | AGCAAGCTCCATAGC[C/G]TCTGTGGGCCTGGCC | 5336 |
| rs192793203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850885 | AATAGGGTTAACTCC[C/T]TTGAGTAAGATTTAA | 5336 |
| rs192827728 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944708 | CTTGAATTCCTGGCT[A/T]CAAGTGATCCTCCTG | 5336 |
| rs192847599 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927870 | AAAGGTGTGGCAGTG[G/T]GAATGTGGTTGTGTT | 5336 |
| rs192861919 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902831 | CAATCATGTCAGAAG[A/G]CAAAGGAGGAGCAAA | 5336 |
| rs192864888 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785184 | TTTTGGGCCCAAGCA[C/T]CTCTCTGACACTGAC | 5336 |
| rs192869175 | snp | C/G | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879244 | GGAAGTGTTCTAGCC[C/G]CTGATGCCTTCAGCA | 5336 |
| rs192871084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822574 | CCAGCCTGGCCAATA[G/T]GGCGAAACCCCGTCT | 5336 |
| rs192872267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834303 | TGTTTCTGCCCTGAA[C/G]TTGACCTCGGAGGGC | 5336 |
| rs192875157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853302 | TGCCACTGCACTCCA[C/G]ACTGGGTGACAGAGT | 5336 |
| rs192875397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806351 | TGTGTGATCAGGTAG[C/G]TTTAATTTCCCACAG | 5336 |
| rs192884655 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949412 | TATAAAGGAAACTGA[A/G]TAAGTCTAATATCAG | 5336 |
| rs192900812 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928314 | CTGTTCTAGAATTCA[C/G]AAGGCACGTTTTTAC | 5336 |
| rs192932852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801838 | GTTGTACACCACCAC[A/G]CCTGGTTAATTTTTG | 5336 |
| rs192940102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822936 | GGAAGCAGGTTTTCC[C/T]TCGGAGCCTCCAGAA | 5336 |
| rs192941122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833255 | CCTTTCTGTGGGGGC[C/T]ACAGCCTGGTTGTGT | 5336 |
| rs192975460 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912797 | AAGGGGGAACTTCAG[G/T]TGGAGGCTCACCTGC | 5336 |
| rs192989863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886890 | TTTGCCATTTTCACT[A/G]TTACAGGTATCTAGT | 5336 |
| rs192993950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864801 | ATGGCTGCCTGGGTG[C/T]GGGAGTTGAAGAACC | 5336 |
| rs192995844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797368 | AGGCTCGCAAAATTA[C/T]GTGTCTTGATTTGTC | 5336 |
| rs193002791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819488 | TGGACCTCCTGGCTC[C/T]TCGCCCACTGCTTTT | 5336 |
| rs193003945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839303 | GCAGTTTGAGAAATA[A/G]TGTCATATGGCTCCA | 5336 |
| rs193004340 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958765 | GGAGGCTCTGGCCCC[A/G]CTAGTCCCTCATGGC | 5336 |
| rs193015498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938033 | AACGATCCCCATTCA[C/G]GCAGTGTTTGAGGAT | 5336 |
| rs193030511 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913658 | AGATTGCTTCTTGTG[A/C]AAAATGGGAGGCAGT | 5336 |
| rs193054638 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792776 | CCGGCCCTATGATTC[A/G]ATTACCTCCCACTGG | 5336 |
| rs193054730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871444 | CCCGGGTTCAAGCGA[C/T]TCTTGTGCCTTAGCC | 5336 |
| rs193060474 | snp | A/G | 0.00276688 | 0.0370916 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813763 | GTTCCTTTGTGCAGC[A/G]TCTCTCCCTGTTCTG | 5336 |
| rs193062865 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844818 | TATGTGTGTACACAC[A/G]TGGATGCATACATCT | 5336 |
| rs193084737 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961358 | GTGGAGAAAAGCCCT[C/G]TTTATCTCATTAAGT | 5336 |
| rs193126240 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944340 | ACATATGCAGACTTT[C/T]TTCTTATTCCTTAAT | 5336 |
| rs193128632 | snp | C/T | 6.6257e-05 | 0.00575535 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81939914 | TGGCCTCAGCCCTAT[C/T]TGGGCTCCAACACAG | 5336 |
| rs193131700 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922010 | TGTTAGTAGTGAAGG[A/T]TGTTTTGGCGATGAG | 5336 |
| rs193137700 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879859 | GCCTCTTCATCATGC[A/G]ACAGTTGGCACGGCA | 5336 |
| rs193138226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784736 | CAAAAACATTTAGAT[A/G]GTGGATACTGTTACC | 5336 |
| rs193140788 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896804 | GTGATCATATTGATT[C/G]TTTGCCACAAAGTGA | 5336 |
| rs193156996 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916933 | GTGAGCCACCACGCC[C/T]GGCCAGGACTTTGTT | 5336 |
| rs193166441 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790809 | GGCATTTGGCAAAGT[C/T]TGGAGACGTGTTGAT | 5336 |
| rs193170427 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812005 | TGTAAAAGCATTCCT[A/T]TTTCTCTACATCCTC | 5336 |
| rs193171238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846610 | CATCCAGCAGAACAT[C/T]GGGCTTATGGCTAAT | 5336 |
| rs193206156 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812329 | GCTGAGATTACAGGC[G/T]TGAGCCACCGCACCC | 5336 |
| rs193213569 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947303 | AAATGGAAAGTCGAC[A/G]CTCACAAATCTGCTT | 5336 |
| rs193214612 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926475 | GGATTATGTCCCGTG[C/T]TGTTAGTGTTGTTAT | 5336 |
| rs193217393 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900874 | AGTTCTATGTCCTAC[C/T]GGGCCTGCTCCAGGT | 5336 |
| rs193228768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882018 | GGTGGGGAAAGGTTA[C/G]AATTGTACTCATAAT | 5336 |
| rs193231296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857200 | ATGTCTCCGTCATCC[C/T]TCTCTTCTGGTTTAA | 5336 |
| rs193231948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803730 | TGTGTCGGTCAGGCC[A/G]GAGGGCAGTGGTGCG | 5336 |
| rs193235250 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825081 | GCCTCCAGAAGGAAC[A/T]CAGCCCTGCTGACTC | 5336 |
| rs193284146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955751 | CAACGAAAGTCCCAC[C/G]GATGCGTCTAGTTGG | 5336 |
| rs193286740 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934691 | CGAGTGAGGGAGCTG[C/G]TGGCAGAAGCTTTTT | 5336 |
| rs193287875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910313 | CCAGGCTGGTCTGGA[A/G]CTCCTAATCTCAGGT | 5336 |
| rs193291199 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777922 | CTCAGGAGGCTGAGG[C/G]AGGAGAATCGCTTAA | 5336 |
| rs193291307 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868443 | TCTCTTCACAGTGTC[A/G]GACTAGAGTCAAATT | 5336 |
| rs193291568 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794530 | ATGGTATAAAGAAGG[A/G]CTGTCAAATCCTGGT | 5336 |
| rs193292258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884167 | ACCTACCTGGCCAAC[A/G]TGGTGAAACCCCATC | 5336 |
| rs199514190 | snp | C/G/T | 0.000382644 | 0.0138275 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81900696 | CAAGGAAGTATTTGG[C/G/T]GACCTGCTGTTGACG | 5336 |
| rs199516791 | snp | C/T | 8.29442e-05 | 0.00643935 | missense | PLCG2 | GRCh38.p7 | 16:81919630 | TGAGACTGCGCTACC[C/T]CGTGACCCCCGAGCT | 5336 |
| rs199526555 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830666 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAC | 5336 |
| rs199530350 | snp | C/T | 3.31252e-05 | 0.00406958 | missense | PLCG2 | GRCh38.p7 | 16:81956794 | ACACACCAGAACTTG[C/T]GCAATGCCAACCGGG | 5336 |
| rs199531484 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781028 | GAGACTCCATCTCAA[A/G]ACAAACAAACAAACA | 5336 |
| rs199537366 | snp | C/T | 0.00325364 | 0.0402034 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891421 | AGAAACAAGCAGACA[C/T]CATCCTGCCCGTCAA | 5336 |
| rs199548839 | snp | C/T | 8.28452e-05 | 0.00643551 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928531 | TCCCGTTACAACTAA[C/T]GTGAGTTATGTCTTG | 5336 |
| rs199571184 | snp | C/T | 1.65627e-05 | 0.00287769 | missense | PLCG2 | GRCh38.p7 | 16:81946187 | CAGGATTCAGGTCCG[C/T]TCCTCTGAAGAATGG | 5336 |
| rs199597437 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808650 | AGGTGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 5336 |
| rs199612461 | in-del | -/ACATTTTTTAA | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950631 | TTAGAAAACTTTAAT[-/ACATTTTTTAA]AAATAATGATTTCCT | 5336 |
| rs199617817 | in-del | -/CT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904356 | CAAATCTGGATCTGA[-/CT]CCCCCTATCCTGAGC | 5336 |
| rs199617993 | in-del | -/C | 0.0898077 | 0.191933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851801 | TACAGGCGTGGGCCA[-/C]CAGTGCCCGGCTTGT | 5336 |
| rs199636472 | snp | C/T | 0.00190339 | 0.0307908 | missense | PLCG2 | GRCh38.p7 | 16:81891527 | ATGAGAAGTATGACG[C/T]GGTGGACATGCAGGA | 5336 |
| rs199638859 | snp | C/T | 0.000132474 | 0.00813755 | missense | PLCG2 | GRCh38.p7 | 16:81854515 | CGAGCAAAAGCAGTT[C/T]GCCAGAAAGAAGACT | 5336 |
| rs199642195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900865 | CGTTCACCAAGTTCT[A/G]TGTCCTACTGGGCCT | 5336 |
| rs199643323 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929571 | TGGCTAATTTTTGTA[C/T]TTTTAGTAGAGCTAG | 5336 |
| rs199643936 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81880123 | GCGCATGCCTGTAGT[A/C]CTAGTTACGCAGGAA | 5336 |
| rs199644488 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909587 | CACCTGAATAACTTT[-/G]TAAATTTTTTGTAGA | 5336 |
| rs199650798 | snp | A/G | 0.000248717 | 0.0111488 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869335 | GGGAATTTTATGAAT[A/G]CGGAGTGACTTAGCC | 5336 |
| rs199703276 | snp | C/T | 0.000132501 | 0.00813836 | missense | PLCG2 | GRCh38.p7 | 16:81931569 | AGCAGGGCGATCCTC[C/T]GGTGGAGTTTGCCAC | 5336 |
| rs199705553 | in-del | -/C | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866566 | CAGCATGAGAGGACG[-/C]TGGCCTCTCCCTTGC | 5336 |
| rs199708049 | snp | A/T | 0.000450236 | 0.0149972 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908427 | CCAGGATATACCCCC[A/T]ACAGAACTACATTTT | 5336 |
| rs199732096 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877422 | ATTGCGCCACTGCAC[C/T]CCAGCCTGGGCGACA | 5336 |
| rs199760975 | snp | C/T | 0.000778384 | 0.0197126 | missense | PLCG2 | GRCh38.p7 | 16:81883283 | GGAACACTGACAGGC[C/T]GGATGCCTCTGCTGT | 5336 |
| rs199761977 | snp | A/G | 0.00199792 | 0.0315431 | missense | PLCG2 | GRCh38.p7 | 16:81907721 | GCCATTGCCGATGCC[A/G]AGCTGTCCTTCAGTG | 5336 |
| rs199812621 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916298 | CTTTTTTAAAAAAAG[A/G]AAAAAAACAACGTTT | 5336 |
| rs199835872 | snp | G/T | 1.66568e-05 | 0.00288585 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883354 | CAGGTGAGAGCACAA[G/T]GTGTGTGGGTGCCTG | 5336 |
| rs199840870 | snp | A/G | 0.000248462 | 0.0111431 | missense | PLCG2 | GRCh38.p7 | 16:81936279 | AAGGGCCTGACCCGC[A/G]TCTACCCAAAGGGAC | 5336 |
| rs199846750 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942922 | AAAAACAATTATTTT[-/A]TTTTTTTTTTATACA | 5336 |
| rs199855850 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950997 | ATCAAAAAGGCCAAA[-/T]TTTGTTTTGAGACAG | 5336 |
| rs199879302 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829096 | TCATTAATGGGGTAG[A/T]TAGTAGTTTTTATTT | 5336 |
| rs199902581 | snp | A/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962199 | CTAAGTGATGAATTG[A/T]ATTTGGAAGCAAAAA | 5336 |
| rs199921771 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891996 | CTGGGGATGTGGCTG[A/C]GAACCGGCAGCAGCC | 5336 |
| rs199925488 | in-del | -/C/TC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838085 | AAAGATACTAATTTT[-/C/TC]CTTTTTTTTTTGAGG | 5336 |
| rs199928236 | in-del | -/CCTCCCTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803660 | CTCCCTCCCTCCCTC[-/CCTCCCTT]CCTTCCTTCCTTCCT | 5336 |
| rs199958187 | snp | A/C | 0.000480502 | 0.0154926 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928524 | TTATTATTCCCGTTA[A/C]AACTAACGTGAGTTA | 5336 |
| rs199958718 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825292 | CTCTAATTTTTTTTT[-/G]TTTTTTTTTTTTTTG | 5336 |
| rs199963973 | snp | C/G | 0.000547014 | 0.016529 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895784 | CACACGTGGTATTGA[C/G]GCTGCCGCGTTTCTC | 5336 |
| rs199965581 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855062 | AAAAATACAAAAACT[-/A]AGCTGGGTGTGGTGG | 5336 |
| rs199972098 | snp | C/T | 0.000299172 | 0.0122269 | missense | PLCG2 | GRCh38.p7 | 16:81786000 | CGACAATGTCCACCA[C/T]GGTCAATGTAGATTC | 5336 |
| rs199972153 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932194 | GAAGTGTTTTGGGAA[A/G]GTGTGAGCTTCTGGA | 5336 |
| rs199972766 | in-del | -/G | 0.031825 | 0.122064 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925452 | CTGGAGAAATGGTGC[-/G]GGGGGGGCGTGAAAA | 5336 |
| rs199988921 | snp | A/G/T | 0.000292903 | 0.0120985 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956917 | AAAAACTTTTGGGGG[A/G/T]TCTCTAGGCACGGTG | 5336 |
| rs200016243 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822782 | AAAAAAAAAAAAAAA[C/T]AAAAAGGCAGGAGAT | 5336 |
| rs200025641 | snp | C/G/T | 9.95366e-05 | 0.00705408 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919631 | GAGACTGCGCTACCC[C/G/T]GTGACCCCCGAGCTC | 5336 |
| rs200031932 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827193 | GAGGATTGCTGGGTT[G/T]TTTTTTTTTTGGGGA | 5336 |
| rs200058058 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858439 | TGGGCTACAGGGGGG[A/G]AAAAAAAAAAAAGGG | 5336 |
| rs200081833 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910634 | TGCCCTCATCCAGCA[C/T]TACCGCGAGACGCAC | 5336 |
| rs200086447 | snp | C/T | 0.000132564 | 0.00814031 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883260 | TGCACCCCCTTTCCC[C/T]GAGGATAGGAACACT | 5336 |
| rs200089739 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852485 | GAAGGGACTGGTTGA[-/G]CTTGTTGAGCTTGTG | 5336 |
| rs200096737 | snp | A/C | 0.00214262 | 0.0326607 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957906 | CAGAGTTCAGCACGC[A/C]GCCCATTTCTCATGG | 5336 |
| rs200100973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886409 | TGTGTGCAAATTAGT[A/G]TGCCTTTTCTAGAAA | 5336 |
| rs200106233 | snp | A/G | 0.000149079 | 0.00863235 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881000 | GCTGTGCCGGACCTC[A/G]GTGCCTGGTGCCCAG | 5336 |
| rs200132500 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894040 | TGGTATTAGAGGAAG[A/G]CAAACAGACACCCGC | 5336 |
| rs200135337 | snp | C/T | 0.000118462 | 0.00769527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910759 | GAGGCAGGCGGTGGT[C/T]GGGTTAGCTCCACCA | 5336 |
| rs200135670 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907301 | AGACTAAATTTCATC[-/G]GGGGAAAAAAAAAAG | 5336 |
| rs200137340 | snp | A/G | 0.000483442 | 0.0155399 | missense | PLCG2 | GRCh38.p7 | 16:81900727 | AAGCCCACGGAGGCC[A/G]GTGCTGACCAGCTGC | 5336 |
| rs200141999 | snp | G/T | 0.00184943 | 0.0303528 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900823 | TGTCCAGGGAGCCCA[G/T]TGGCTCGGTTCCCCG | 5336 |
| rs200149635 | snp | C/T | 0.000348233 | 0.0131907 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81893736 | TGACCAGCTGCGGAG[C/T]GAGTCGTCCCCAGAA | 5336 |
| rs200175958 | snp | G/T | 0.471673 | 0.115589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805784 | TTTTTTTTTTTTTTG[G/T]TTTTTTTTTTTTTTG | 5336 |
| rs200176118 | in-del | -/T | 0.029116 | 0.117091 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961082 | AATGGATTTTCCAAG[-/T]TTTTTCTGGTGGTTC | 5336 |
| rs200196592 | in-del | -/ATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906079 | CAAGCTTCTCCAAAT[-/ATT]ATTAATAACATCCTA | 5336 |
| rs200228075 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940574 | TTACAGTTTTCTTCC[C/G]TGCTGAAGAAAACAC | 5336 |
| rs200250244 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906087 | GTTATGTAGGATGTT[A/G]TTAATAATATTTGGA | 5336 |
| rs200269364 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926785 | GTGAACTTTTGTCTT[C/G]TATGGTCTCTGACTT | 5336 |
| rs200274958 | snp | C/G | 0.00299551 | 0.0385848 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912759 | TCTACAGAGGGGCTT[C/G]GCAAGGACAGATGCG | 5336 |
| rs200276965 | in-del | -/GATG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927733 | GTTTATTTTCTAAGG[-/GATG]TAGGGCAATCTGGGA | 5336 |
| rs200277154 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816496 | TAATTTTTTTTTTTT[G/T]AGACACGGTCTCATT | 5336 |
| rs200278332 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835600 | AATAATAATAATAAT[A/C]ATAATAATAATGATA | 5336 |
| rs200303846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915772 | ACCTTGGCTCTGTAC[C/T]TCGGCACCCCAGAGC | 5336 |
| rs200312530 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876038 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGGGT | 5336 |
| rs200316407 | in-del | -/C | 0.0209421 | 0.100162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824246 | TCAAGCAATTCTCCT[-/C]CCTCAGCCTCCCAAG | 5336 |
| rs200325678 | snp | A/G | | | missense | PLCG2 | GRCh38.p7 | 16:81910531 | GCAGGCGGTCAGGCC[A/G]GGTCCAGCACTGCCG | 5336 |
| rs200343785 | snp | A/C | 1.67253e-05 | 0.00289178 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940106 | TGGGCTGGCGTTGTA[A/C]TTTGGTTTGGCTGCT | 5336 |
| rs200351874 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936440 | CAGTCACTCCAGGCC[A/G]AGTCACCTTGGGTCA | 5336 |
| rs200354151 | snp | A/C/G | 0.00010577 | 0.00727143 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889307 | TTGTCGCTTGGGGGT[A/C/G]ACTTTTTGATTGATG | 5336 |
| rs200356569 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787855 | GTGACTGGCTTCTTT[A/C]ACTCAGCATTTTTCA | 5336 |
| rs200366770 | snp | A/C/G | 6.64224e-05 | 0.00576259 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937897 | CCTGATGACGCTGAC[A/C/G]GTCAAGGTAAAGCCA | 5336 |
| rs200389119 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857029 | AGATCTCATGCAACC[-/AA]AGTCTATTTTAGACT | 5336 |
| rs200398920 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885640 | TTTTTTTTTTAAAAT[A/T]TAGCCATAACACTCC | 5336 |
| rs200406640 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858120 | CCATGACGGTGTGAA[A/G]GGGGATGCTTTCTTT | 5336 |
| rs200425954 | snp | A/C/G | 0.000170745 | 0.00923844 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907664 | GACTTGGGGGGCACT[A/C/G]ATACCAGTTTCACTT | 5336 |
| rs200449944 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888389 | CTGATTTAAAGAAAA[A/G]AAAAATGTTTGTATT | 5336 |
| rs200459426 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804317 | ATTGCTCTATCTTAA[A/G]TAGTTGATGTAATAA | 5336 |
| rs200464512 | snp | A/G | 0.000182169 | 0.00954208 | missense | PLCG2 | GRCh38.p7 | 16:81869239 | CGAGAGTTGAAGACC[A/G]TCTTGCCCCTGATCA | 5336 |
| rs200466053 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942920 | AGAAAAACAATTATT[-/A]TTTTTTTTTTTTATA | 5336 |
| rs200481178 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809972 | TCTGCCAGTCTTTGT[C/G]TGCCACCATGGTTCT | 5336 |
| rs200484243 | snp | A/G | 0.000199094 | 0.00997534 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891448 | TCAACGTGATGATTC[A/G]GTCTTCGTGTTTGAC | 5336 |
| rs200493094 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909037 | AGCCGTCATAGGCTG[G/T]GATGAGCTTGTGCAT | 5336 |
| rs200506549 | snp | A/G | 0.00245867 | 0.0349756 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81893709 | CCTTCTCTCCTGCAG[A/G]TACCTTACAGGTGAC | 5336 |
| rs200511055 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860176 | TATTATTATTATTTT[-/A]TTTTTTTTTTTGTAA | 5336 |
| rs200529725 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851803 | CAGGCGTGGGCCACC[-/A]GTGCCCGGCTTGTTT | 5336 |
| rs200533453 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859541 | TTCTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 5336 |
| rs200535880 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782689 | CCAGAAATCAAGGAA[-/G]GTTTTTCTCTTCAGT | 5336 |
| rs200568068 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805127 | AAGAGGTTAACAAGA[G/T]AAGCCACAGATAGGG | 5336 |
| rs200573080 | snp | C/G | 0.00039954 | 0.0141284 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854408 | CAGGTGGAGGGAACT[C/G]CAGCTTCTAATTGGC | 5336 |
| rs200594841 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858096 | TCAGACAAAAAGCAG[C/T]TCCTAGGGCCATGAC | 5336 |
| rs200609506 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901868 | TATTTAATATCTTAA[A/T]CATGTTTCAATATAA | 5336 |
| rs200649912 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953907 | ATTTTGAACTTGCGC[C/T]CGAATAACAAATACC | 5336 |
| rs200653510 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858437 | CATGGGCTACAGGGG[A/G]GAAAAAAAAAAAAAG | 5336 |
| rs200676347 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781052 | ACAAACAAACAAACA[A/C]ACACAAACACTTCTT | 5336 |
| rs200677528 | snp | C/G | 0.00024849 | 0.0111438 | missense | PLCG2 | GRCh38.p7 | 16:81931546 | TGTCTTCATCCTGGA[C/G]CCCAAGCAGCAGGGC | 5336 |
| rs200684966 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849433 | TGTATAATTTTTCTG[G/T]AAGGACAGATGCTCA | 5336 |
| rs200736474 | snp | A/G | 0.00199792 | 0.0315431 | missense | PLCG2 | GRCh38.p7 | 16:81908449 | CTACATTTTGGGGAG[A/G]AATGGTTCCACAAGA | 5336 |
| rs200760958 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941578 | TTTTTTTTTTTTTTT[-/T]GTACTCTAGAAATGT | 5336 |
| rs200788818 | snp | A/G | 2.40856e-05 | 0.00347019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908633 | TACCTTCTTCTCCAT[A/G]CCAACCGATGAGGCA | 5336 |
| rs200790127 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962228 | AAGGATGGCTAAAAA[A/G]GACCTCAACCCTTTT | 5336 |
| rs200794987 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962197 | CACTAAGTGATGAAT[C/T]GTATTTGGAAGCAAA | 5336 |
| rs200800716 | snp | C/G | 0.000199256 | 0.0099794 | missense | PLCG2 | GRCh38.p7 | 16:81956854 | GAGAACCAGCTCCAG[C/G]TGTACCAGGAGAAAT | 5336 |
| rs200800971 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797282 | GGTGAATCATTTTTG[C/T]AAAAAAAAAAATTAT | 5336 |
| rs200808320 | in-del | -/C | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913817 | GACCCTGCCAGGCTG[-/C]CCCCTGGGCGTTTGG | 5336 |
| rs200813182 | snp | C/T | 0.00112551 | 0.0236958 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937817 | CGCACGGGCTACGTT[C/T]TGCAGCCTGAGAGCA | 5336 |
| rs200824224 | snp | A/G | 0.000132575 | 0.00814065 | missense | PLCG2 | GRCh38.p7 | 16:81893771 | ACATCCGCTGCCTGC[A/G]CATGGGCTGTCGCTG | 5336 |
| rs200824503 | snp | A/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962203 | GTGATGAATTGTATT[A/T]GGAAGCAAAAAGGAT | 5336 |
| rs200831991 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920755 | GCTCTCAGCGGGGTA[A/G]GGGGAAGGCACTGGT | 5336 |
| rs200832210 | snp | C/T | 0.000101213 | 0.0071131 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956890 | AAGAGGTAGGTCAGC[C/T]CCTCCACCTGCAAAA | 5336 |
| rs200841428 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942931 | TATTTTTTTTTTTTT[-/A]TATACAAGGAGGGCT | 5336 |
| rs200842061 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866714 | AGGATGGGCTCCACT[-/G]GGGCACCAGCATGAG | 5336 |
| rs200844173 | snp | A/G | 0.000198791 | 0.00996774 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81927091 | ATCCAGGTGGAAAGG[A/G]GACTATGGAACCAGG | 5336 |
| rs200846103 | snp | A/G/T | 3.45885e-05 | 0.00415852 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958026 | GTGTGTAAGGGTATT[A/G/T]TGTGTGTGCGCATGT | 5336 |
| rs200853258 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782244 | ATGAGATACAAGAAA[A/G]ACCTTTAGAAGGACA | 5336 |
| rs200871705 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810640 | TATTTTCTGCAATTT[C/T]TTTCTTTTTATTTTT | 5336 |
| rs200875985 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934702 | GCTGGTGGCAGAAGC[-/T]TTTTTGGTGTATTAG | 5336 |
| rs200892679 | snp | C/T | 6.67e-05 | 0.00577456 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910504 | TCCCAGCACTGATGG[C/T]GTCCTCTCCCCGCAG | 5336 |
| rs200906229 | in-del | -/ACAAAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858085 | GTGGCCCCATCTCAG[-/ACAAAAA]GCAGGTCCTAGGGCC | 5336 |
| rs200906847 | in-del | -/TTTA | 0.422944 | 0.180528 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841205 | GGCCAAAAAGTAAAC[-/TTTA]TTTATTTATTTATTT | 5336 |
| rs200919414 | snp | C/T | 0.000472534 | 0.0153637 | missense | PLCG2 | GRCh38.p7 | 16:81900760 | TCGCCCAGCCAGCTG[C/T]GGGAGAAGATCATCA | 5336 |
| rs200931278 | snp | A/T | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778831 | TTTATTTATTTATTT[A/T]TGAGACGGAGTGTCT | 5336 |
| rs200945548 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789852 | CACCTTTGCCCCCCC[-/T]CCATTGCCTCCCCTC | 5336 |
| rs200958396 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869122 | AGGCTCTCTCATAGA[-/G]GGCTGCCTGAGGTGG | 5336 |
| rs200958920 | snp | C/T | 0.00199809 | 0.0315444 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919681 | TAGGTGGTGGACTCC[C/T]TTGTGATTTGGTGGG | 5336 |
| rs200981336 | snp | A/G | 0.000298072 | 0.0122044 | missense | PLCG2 | GRCh38.p7 | 16:81869267 | TCAACTTTAAAGTGA[A/G]CAGTGCCAAGTTCCT | 5336 |
| rs200981948 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888385 | CAAGCTGATTTAAAG[A/G]AAAAAAAAATGTTTG | 5336 |
| rs200982591 | in-del | -/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899264 | GCCTCAGGAGGAGTA[-/TG]TGTGTGTATATATAT | 5336 |
| rs201020357 | snp | A/G/T | 0.00116417 | 0.0241003 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912755 | ATGCTCTACAGAGGG[A/G/T]CTTGGCAAGGACAGA | 5336 |
| rs201023271 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925892 | CTCTGTCTCAAAAAA[A/G]AAAAAAAAAAAATCC | 5336 |
| rs201043827 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874967 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTATTTG | 5336 |
| rs201045382 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876019 | TCTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 5336 |
| rs201053730 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869125 | CTCTCTCATAGAGGG[C/G]TGCCTGAGGTGGGAA | 5336 |
| rs201080992 | snp | A/C/G | 0.00224166 | 0.0334037 | missense | PLCG2 | GRCh38.p7 | 16:81870866 | GGAAATAGGAGCACA[A/C/G]AAAGATGAGCTCAGC | 5336 |
| rs201084625 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919607 | GAAGCATTCACTCTA[C/T]CGAAAGATGAGACTG | 5336 |
| rs201085570 | snp | C/G | 0.00199796 | 0.0315435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895751 | GGGCCGGGGGCTGAC[C/G]TCGGGGCTGTCAGTG | 5336 |
| rs201100463 | in-del | -/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885054 | CACCATGCCTGACAA[-/TT]TTTTTTTTTTTTTTG | 5336 |
| rs201106616 | snp | C/G | 5.10869e-05 | 0.00505379 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889142 | TCAGTTCTCACTTTG[C/G]TGATCTCTCGTTCTC | 5336 |
| rs201110214 | snp | A/G/T | 0.000597426 | 0.0172732 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936388 | CGGCAGGTAAAGGCC[A/G/T]ACTGAAGGTAGTCCC | 5336 |
| rs201115487 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942581 | TGGAGCGCAGGAAGG[-/A]AAAGCAGCAGCCTTT | 5336 |
| rs201155140 | in-del | -/CCT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781861 | CATCTCATTTCATGT[-/CCT]TTCCCCCCCCCCCCC | 5336 |
| rs201155403 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803135 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAATCTCA | 5336 |
| rs201215284 | snp | C/T | 0.000184188 | 0.0095948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931672 | AGGCACCTGCTCACC[C/T]GGGTGCAGGTGGGCC | 5336 |
| rs201243141 | snp | C/T | 8.72258e-05 | 0.00660343 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908622 | CAGGGAACGCCTACC[C/T]TCTTCTCCATGCCAA | 5336 |
| rs201247651 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916256 | GCTTAAAGCAATATA[-/T]TTTTTTTTTTCAAAA | 5336 |
| rs201248680 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955625 | CTCAGTGGCTGTTTT[A/G]CTCTTTTTCTGGCAC | 5336 |
| rs201274263 | snp | A/G/T | 0.000264969 | 0.0115073 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858384 | TGCCTGTTGATTTGC[A/G/T]TAGTTGCTGATTCCT | 5336 |
| rs201282710 | snp | C/G | 1.72949e-05 | 0.0029406 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786194 | TTCTGTGAGTACTCG[C/G]TGGGTGGGGCAGTGT | 5336 |
| rs201294738 | snp | C/T | 0.000249715 | 0.0111712 | missense | PLCG2 | GRCh38.p7 | 16:81870934 | TTGAACAGCAAAAAT[C/T]GGTAAGATGATTCTT | 5336 |
| rs201306895 | in-del | -/TG/TTG | 0.370974 | 0.218781 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803134 | TTTTTTTTTTTTTTT[-/TG/TTG]GTGAGACGGAATCTC | 5336 |
| rs201318091 | snp | A/T | 0.00199806 | 0.0315443 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956781 | CTTTCTGTATGACAC[A/T]CACCAGAACTTGCGC | 5336 |
| rs201333148 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916297 | CCTTTTTTAAAAAAA[A/G]AAAAAAAACAACGTT | 5336 |
| rs201335296 | in-del | -/A | 0.0138799 | 0.0821421 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961099 | TTTTCTGGTGGTTCC[-/A]AATTTTTTGCTTTCA | 5336 |
| rs201371631 | snp | G/T | 0.00416137 | 0.0454243 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921394 | CTGGCCAAAATAATT[G/T]TTTTTTTTTTTTGAG | 5336 |
| rs201391996 | snp | A/G | 6.71456e-05 | 0.00579382 | missense | PLCG2 | GRCh38.p7 | 16:81908417 | TCTTTGCGGCCCAGG[A/G]TATACCCCCTACAGA | 5336 |
| rs201403309 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851575 | TGGAGTGCAGTGGCG[G/T]GGTCTCGGCTCCCTG | 5336 |
| rs201409875 | snp | C/T | 0.000134106 | 0.00818749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912575 | CGCTCACCTGGTCGT[C/T]TTCCCTGGCCCTGTG | 5336 |
| rs201410855 | snp | C/T | 0.000161948 | 0.00899709 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938785 | GGGGTTCCAATGCTT[C/T]CCTTTGGTGTCCCAG | 5336 |
| rs201412321 | snp | G/T | 0.000463768 | 0.0152207 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928544 | AACGTGAGTTATGTC[G/T]TGTTTCTTCACAGAT | 5336 |
| rs201431172 | in-del | -/TCCTGTCCTGTCCTGTCCTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824047 | TCCTTTCCTTTCCTT[-/TCCTGTCCTGTCCTGTCCTG]TCCTGTCCTGTCCTG | 5336 |
| rs201475640 | snp | A/G | 4.96816e-05 | 0.00498381 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81939974 | AAACCTGGCATTTCT[A/G]CGCTTTGTGGTTTAT | 5336 |
| rs201487295 | snp | C/T | 1.72047e-05 | 0.00293293 | missense | PLCG2 | GRCh38.p7 | 16:81870916 | TCTATAAAAAACTTA[C/T]GTTTGAACAGCAAAA | 5336 |
| rs201490178 | snp | A/G | 0.00858254 | 0.0649431 | missense | PLCG2 | GRCh38.p7 | 16:81900676 | CGTCACATGGCCAAG[A/G]CCTTCAAGGAAGTAT | 5336 |
| rs201492291 | in-del | -/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825291 | GCTCTAATTTTTTTT[-/TG]TTTTTTTTTTTTTTT | 5336 |
| rs201501711 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929564 | CCGTGCCTGGCTAAT[G/T]TTTGTATTTTTAGTA | 5336 |
| rs201515331 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830662 | GGTGTGTGTGTGTGT[A/G]TGTGTATATATATAT | 5336 |
| rs201526187 | in-del | -/C | 0.078151 | 0.181571 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941698 | CCCACACTGTAAACT[-/C]CCCCCTTTTTTTTTT | 5336 |
| rs201548435 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781096 | GCAAGAACACAAAGA[-/G]AAAAATTTGCCCGTT | 5336 |
| rs201569432 | in-del | -/TC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893431 | GTGCTTTGACCAACT[-/TC]TCCTCAAAAGAACAC | 5336 |
| rs201575604 | in-del | -/GCT | 0.0869089 | 0.189476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934804 | TCACAGTTCCACGTG[-/GCT]GAGGAGGCCTCACAA | 5336 |
| rs201578091 | in-del | -/GCTCCACTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865796 | TTGCTCCCAGGATGG[-/GCTCCACTG]GGCACCAGCATGAGA | 5336 |
| rs201591234 | snp | C/T | 3.3484e-05 | 0.00409156 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919661 | CCTGGAGCGCTACAA[C/T]ATGGTAGGTGGTGGA | 5336 |
| rs201601191 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909039 | CCGTCATAGGCTGTG[A/G]TGAGCTTGTGCATTC | 5336 |
| rs201601618 | snp | C/G | 1.6563e-05 | 0.00287771 | missense | PLCG2 | GRCh38.p7 | 16:81931576 | CGATCCTCCGGTGGA[C/G]TTTGCCACAGACAGG | 5336 |
| rs201608031 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870776 | TTTCTGAAACAAAAA[A/T]TATTCTATAAATAGC | 5336 |
| rs201622146 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962198 | ACTAAGTGATGAATT[A/G]TATTTGGAAGCAAAA | 5336 |
| rs201647862 | snp | A/G | 4.96824e-05 | 0.00498385 | missense | PLCG2 | GRCh38.p7 | 16:81937832 | CTGCAGCCTGAGAGC[A/G]TGAGGACAGAGAAAT | 5336 |
| rs201652976 | snp | C/T | 0.00282777 | 0.0374952 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895841 | CGATGGGAAGCCGGT[C/T]ATCTACCATGGCTGG | 5336 |
| rs201654184 | snp | A/C | 0.000380829 | 0.0137938 | missense | PLCG2 | GRCh38.p7 | 16:81895894 | TTGACGACGTCGTGC[A/C]GGCCATCAAAGACCA | 5336 |
| rs201659233 | snp | A/C/T | 0.000150215 | 0.00866526 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931662 | ACACCAAGGTAGGCA[A/C/T]CTGCTCACCCGGGTG | 5336 |
| rs201682723 | snp | A/C/G | 0.000822672 | 0.020265 | synonymous-codon, missense | PLCG2 | GRCh38.p7 | 16:81956697 | CTGCATCCTCCAGGA[A/C/G]AGCGAAGAGGAACTT | 5336 |
| rs201686722 | snp | A/C/T | 0.000421429 | 0.0145101 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883380 | GCCTGAGGGAGCTGG[A/C/T]GGGATGCTGCTGGGG | 5336 |
| rs201690010 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866142 | CCCAGGGTGAGCTCC[-/A]ACTGGGGCACCAGCA | 5336 |
| rs201711190 | in-del | -/AC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907016 | CACTCCAGCCTGGTG[-/AC]AGAGAGACAGACTCT | 5336 |
| rs201728236 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860177 | ATTATTATTATTTTT[-/A]TTTTTTTTTTGTAAA | 5336 |
| rs201746780 | snp | A/G | 0.000336865 | 0.0129738 | missense | PLCG2 | GRCh38.p7 | 16:81905489 | GGGGGAGCTGTACAT[A/G]TGGGATTCCATTGAC | 5336 |
| rs201749224 | snp | C/T | 0.00256086 | 0.0356913 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893670 | CCCCAACCCCTGTGG[C/T]TGCCACTCTCACACG | 5336 |
| rs201753773 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789849 | CCCACCTTTGCCCCC[-/A]CCTCCATTGCCTCCC | 5336 |
| rs201762281 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916089 | TAGAAAATACAAATG[G/T]GAACATTCTGCAGCT | 5336 |
| rs201777471 | snp | A/C/T | 0.000164159 | 0.00905838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905538 | TTCCCGTAGCCACTG[A/C/T]GGCCACGCCCCTTGC | 5336 |
| rs201778389 | snp | C/T | 3.49773e-05 | 0.00418179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956928 | GGGGGTCTCTAGGCA[C/T]GGTGATGATGGGCAC | 5336 |
| rs201791343 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796843 | TGGTCTCCAGAACTG[-/T]GAGACAAACTTCTGT | 5336 |
| rs201800990 | in-del | -/TACATTTTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950630 | GTTAGAAAACTTTAA[-/TACATTTTT]TAAAAATAATGATTT | 5336 |
| rs201801906 | snp | A/C/T | 0.000270311 | 0.0116228 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958035 | GGTATTGTGTGTGTG[A/C/T]GCATGTGTGTTTGCA | 5336 |
| rs201803492 | snp | A/G | 0.00017666 | 0.00939674 | missense | PLCG2 | GRCh38.p7 | 16:81923489 | TTCCCTGAAAGCCTC[A/G]GAGAACCGTGAAAGC | 5336 |
| rs201808665 | in-del | -/A/GA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832104 | TCCTTTGATAAATGG[-/A/GA]AGGGGGGGAATAGTG | 5336 |
| rs201809622 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888039 | ATTTGGAGCTGAGAC[A/T]CTGCAGTTTACAAGC | 5336 |
| rs201812767 | in-del | -/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782690 | CAGAAATCAAGGAAG[-/GT]TTTTTCTCTTCAGTG | 5336 |
| rs201820658 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916593 | CCATTTTTTTTTTGT[G/T]TGTGGTGAGACTTAA | 5336 |
| rs201826443 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962204 | TGATGAATTGTATTT[G/T]GAAGCAAAAAGGATG | 5336 |
| rs201830291 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941720 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 5336 |
| rs201837004 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841792 | GTGTATCTCACCTAT[C/T]CCCCCAGCTGCCATG | 5336 |
| rs201867136 | in-del | -/TGTGTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830663 | GTGTGTGTGTGTGTG[-/TGTGTA]TATATATATATACAC | 5336 |
| rs201917839 | snp | C/T | 8.31456e-05 | 0.00644716 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910515 | ATGGCGTCCTCTCCC[C/T]GCAGGCGGTCAGGCC | 5336 |
| rs201929574 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805292 | ATCACAAGGTCAGGA[A/G]ATCGAGACCATCCTG | 5336 |
| rs201944343 | snp | A/G | 0.00066223 | 0.0181845 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880975 | CAGCTCTTGTGTGTC[A/G]TTCGGGGCGGCTGTG | 5336 |
| rs201945178 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874027 | CCCGTGTGGAACTTT[G/T]TATGGCAAAGATTCT | 5336 |
| rs201949878 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834588 | TAGACCCTGGATCTG[C/T]AGAGCTGCTGCTGCT | 5336 |
| rs202002041 | snp | A/G | 1.65982e-05 | 0.00288077 | missense | PLCG2 | GRCh38.p7 | 16:81786006 | TGTCCACCACGGTCA[A/G]TGTAGATTCCCTTGC | 5336 |
| rs202065168 | in-del | -/A | 0.144969 | 0.226867 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877298 | CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCTG | 5336 |
| rs202068485 | snp | A/G | 0.0040556 | 0.0448481 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858438 | ATGGGCTACAGGGGG[A/G]AAAAAAAAAAAAAGG | 5336 |
| rs202075259 | in-del | -/GTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871886 | CTGGGTAAATTATGG[-/GTC]TCTATCCATATTATG | 5336 |
| rs202103803 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857520 | CAAGATCAAGATGCT[A/G]GATGGTTGAGTTCTG | 5336 |
| rs202108152 | snp | C/T | 4.96907e-05 | 0.00498426 | missense | PLCG2 | GRCh38.p7 | 16:81956806 | TTGCGCAATGCCAAC[C/T]GGGATGCCCTGGTTA | 5336 |
| rs202110243 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888384 | CCAAGCTGATTTAAA[-/G]AAAAAAAAAATGTTT | 5336 |
| rs202120968 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827192 | GAGGATTGCTGGGTT[-/G]TTTTTTTTTTTGGGG | 5336 |
| rs202144513 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929561 | CCACCGTGCCTGGCT[A/G]ATTTTTGTATTTTTA | 5336 |
| rs202165223 | in-del | -/AACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781051 | ACAAACAAACAAACA[-/AACA]CACACAAACACTTCT | 5336 |
| rs202166689 | snp | C/G/T | 0.000384606 | 0.013862 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937739 | CTGACTTACAGCAGG[C/G/T]GTTCACTTTCCTTCC | 5336 |
| rs202192451 | in-del | -/TTCTT | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954328 | CGCCCGGCGACTTGA[-/TTCTT]TTCTTTTCTTTTTCC | 5336 |
| rs202193221 | snp | A/G | 0.000713976 | 0.0188806 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912740 | GAGGGTGGGAGGCAC[A/G]TGCTCTACAGAGGGG | 5336 |
| rs202196694 | in-del | -/AT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842192 | CAGAACTCCCTACAA[-/AT]AGGGAGGCTTTCTCC | 5336 |
| rs202201104 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782696 | ATCAAGGAAGTTTTT[-/C]TCTTCAGTGCTCTGT | 5336 |
| rs202207822 | in-del | -/TGATCTTACTTTAAA | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942841 | CAAAGCCAGATGCAT[-/TGATCTTACTTTAAA]TGATCTTACTTTAAA | 5336 |
| rs202210217 | snp | A/G | 1.70507e-05 | 0.00291977 | missense | PLCG2 | GRCh38.p7 | 16:81923552 | AGCTGAGCTTCTGCC[A/G]TGGTGCCCTCATCCA | 5336 |
| rs202213718 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829610 | CAGAATTTATTTGGA[-/C]TTTAACAGTTTCTCC | 5336 |
| rs202214266 | snp | C/G/T | 0.00019914 | 0.00997669 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936387 | ACGGCAGGTAAAGGC[C/G/T]GACTGAAGGTAGTCC | 5336 |
| rs202234501 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865780 | GACGCTGGCCTCTCC[A/C]TTGCTCCCAGGATGG | 5336 |
| rs202246508 | in-del | -/G/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916590 | AACCATTTTTTTTTT[-/G/TG]GTGTGTGGTGAGACT | 5336 |
| rs267604657 | snp | C/T | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81880945 | GGATTCGTCCGTGTT[C/T]ATCCTGGGGTGAGGC | 5336 |
| rs367560125 | snp | G/T | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963041 | AATCACTGCGTTTCT[G/T]GCCAACAATCCCTGG | 5336 |
| rs367563792 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906089 | CAAATATTATTAATA[A/T]CATCCTACATAACCA | 5336 |
| rs367564287 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840582 | GGCATTAGATTCTCA[A/T]AAAGAGTGTACAACC | 5336 |
| rs367565679 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876813 | CACATAACCCTCCAT[G/T]GTAATGCCGAACATA | 5336 |
| rs367581596 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863559 | ATTCCTCTGTGTATA[C/T]ATCCAGAAGCTGAAT | 5336 |
| rs367586328 | snp | C/T | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778295 | GGATCGCTTGAGTCC[C/T]GGAGTTCGAGGATGT | 5336 |
| rs367599078 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914102 | GAGGTGTGTTCAGTC[C/T]GCTGCACACGGATTG | 5336 |
| rs367603065 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797060 | GTGTCATGTTATTTT[C/G]TAGCTGCGTTGGTTC | 5336 |
| rs367618764 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81898838 | ACCTGTGGGGGATGT[C/G/T]TGCGCCTTATTTCAG | 5336 |
| rs367633550 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814860 | GGGGATTATGATGAT[A/C]CTCTCCCCATAGAGT | 5336 |
| rs367649147 | snp | C/T | 0.00022687 | 0.0106482 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956926 | TGGGGGGTCTCTAGG[C/T]ACGGTGATGATGGGC | 5336 |
| rs367651729 | in-del | -/ATAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838779 | TTAAAGTAAAATTAA[-/ATAT]ATATATATATATATA | 5336 |
| rs367654927 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961172 | CATGTAACTACAAAG[A/G]GGTTGGAAGAATTCA | 5336 |
| rs367671782 | snp | A/G | 1.72362e-05 | 0.00293561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936140 | AGATGAGACACAGAA[A/G]TACTGATGACCTTTT | 5336 |
| rs367677388 | snp | C/T | 0.00173773 | 0.0294253 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919577 | GAGTCTGGTGGAGCT[C/T]GTCAGTTACTACGAG | 5336 |
| rs367678289 | snp | C/G/T | 4.99474e-05 | 0.00499716 | missense | PLCG2 | GRCh38.p7 | 16:81900710 | GCGACCTGCTGTTGA[C/G/T]GAAGCCCACGGAGGC | 5336 |
| rs367679252 | snp | C/T | 3.69426e-05 | 0.00429767 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938764 | CTGCCTGTTCAGGAC[C/T]CCAGGGGGGTTCCAA | 5336 |
| rs367682005 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927036 | CAGTAGTGGGTAATT[C/T]ATGCCACCTGGTGAC | 5336 |
| rs367704973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903781 | CCATTAGGATGGCTT[C/G]CTGCCTGTTCCCAGG | 5336 |
| rs367716839 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902924 | AGATCTCATGAGATG[C/T]GTTCACTATCACAAG | 5336 |
| rs367733121 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913823 | GCCAGGCTGCCCCCT[C/G]GGCGTTTGGATTTCC | 5336 |
| rs367737859 | in-del | -/TAAAA | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861179 | ACCTTATTTTTTTGG[-/TAAAA]TATTCCTTTCATTCA | 5336 |
| rs367738475 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854804 | GTGAAATGGGGAGAA[A/T]AATAATGCCTATTTC | 5336 |
| rs367745602 | in-del | -/TGAG | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778356 | GCCTGGGTGACAGAG[-/TGAG]ACCCTGCCTCTTAGA | 5336 |
| rs367751699 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838376 | ACAGGCATGAGCCGC[C/T]GTTGCCAGCCTGAAA | 5336 |
| rs367779682 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832499 | GGTTCAAGCTATCTT[C/T]CCACCTCAGCCTCCC | 5336 |
| rs367786769 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959225 | GTGGTGGGGAAGAAC[A/G]AACCAGCAGTAAGCC | 5336 |
| rs367791114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823329 | CTCTCTCGACAGAAA[C/T]GCAGAAGTGAGCTGC | 5336 |
| rs367796511 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780564 | CAGGGACAATCGTCA[C/T]TGTGAGCCTCACTGA | 5336 |
| rs367815706 | in-del | -/GAGG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930646 | CAGCTACTAGGGAGG[-/GAGG]CTGAGGTGGGAGGAT | 5336 |
| rs367855637 | snp | C/T | 0.000117482 | 0.00766337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937728 | CGTGCTCATGCCTGA[C/T]TTACAGCAGGCGTTC | 5336 |
| rs367858701 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934075 | TGAAGAACTAGAATT[G/T]GAGACACTCTAACAG | 5336 |
| rs367864083 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949576 | CATGTATCCTACTCA[A/G]GGGAAATCTTGAGGC | 5336 |
| rs367866295 | snp | C/G | 1.65627e-05 | 0.00287769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928634 | ACGTCGGTACGTGCA[C/G]ACATCATCTTAGCCT | 5336 |
| rs367870246 | in-del | -/CA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81880572 | GTAAAGCTTGAAACA[-/CA]GCAAAAAATTGTGAG | 5336 |
| rs367870963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926802 | ATGGTCTCTGACTTC[C/T]ACGTAAAGCATGGAA | 5336 |
| rs367874879 | snp | C/G | 8.28397e-05 | 0.00643529 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946150 | AATTACCTGCCTTTG[C/G]ATTTTCCTCCTTGTT | 5336 |
| rs367884906 | snp | A/G | 0.000159987 | 0.00894249 | missense | PLCG2 | GRCh38.p7 | 16:81910710 | AACCCCAACCCCCAC[A/G]AGTCCAAGCCGTACG | 5336 |
| rs367885048 | snp | A/G | 0.000132474 | 0.00813755 | missense | PLCG2 | GRCh38.p7 | 16:81858331 | CAGGAAGCGATGAAT[A/G]CGTCCACGCCCACCA | 5336 |
| rs367898185 | snp | A/G | 3.3484e-05 | 0.00409156 | missense | PLCG2 | GRCh38.p7 | 16:81870861 | TTACAGGAAATAGGA[A/G]CACACAAAGATGAGC | 5336 |
| rs367901037 | in-del | C/TA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870770 | ATGCCATTTCTGAAA[C/TA]AAAAATTATTCTATA | 5336 |
| rs367922513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901056 | AGGCGTGCAGAATGC[A/G]TGCAACTGCGCCTGT | 5336 |
| rs367929772 | snp | C/T | 5.18453e-05 | 0.00509116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921296 | AACCTCCAATTCACA[C/T]GATTTTGGAGTCACG | 5336 |
| rs367930737 | snp | C/G | 0.000489862 | 0.0156426 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907812 | TAGGGAGGAGGTCCC[C/G]AGGAACCCCGAGGAC | 5336 |
| rs367936087 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801552 | ACATTTAGGTTGTTT[C/G]CAATCATGATACTCC | 5336 |
| rs367943688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944765 | ACAGGCATGAGCCAC[C/T]GTACTTGGCCAACTA | 5336 |
| rs367943919 | snp | A/G | 0.000155988 | 0.00883004 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893844 | CAGCAAATTGAGGAT[A/G]ACCATGTGGTTGCTC | 5336 |
| rs368008897 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866988 | AGCTGGCCCAACAGG[A/G]ACTTTTTCTGCCCTC | 5336 |
| rs368009623 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811468 | TCAGGATGATGTTTC[C/T]GTTTTCTTTTTTCTT | 5336 |
| rs368032114 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778598 | AACGGGACATCAATT[A/G]TCTGGGGTTCTTTGC | 5336 |
| rs368036121 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789711 | TATAATAAGTCCCCC[A/G]GATGGTCTGGTAACT | 5336 |
| rs368071289 | snp | A/C/G | 3.38914e-05 | 0.00411638 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81938863 | TCCCTTTGTAGAAGT[A/C/G]GAGATCTGTGGAGCC | 5336 |
| rs368107827 | snp | C/T | 8.28397e-05 | 0.00643529 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81891483 | TTAGTTCCTCACGTA[C/T]CTGTTTTCACGAGAA | 5336 |
| rs368125576 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782110 | CTTGATCTCCTGACC[-/T]CATGATCCGCCCACC | 5336 |
| rs368136839 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890314 | TATTTTGGGGGAAGG[A/G]CTGGTATTTAAACTA | 5336 |
| rs368137889 | snp | G/T | 1.65663e-05 | 0.002878 | missense | PLCG2 | GRCh38.p7 | 16:81786122 | CGGAGAACCGTCCAG[G/T]TGATCATGGAGACGC | 5336 |
| rs368139970 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828022 | TTGCACCTGGGAGGC[A/G]GAGCTTGCACTGAGC | 5336 |
| rs368147709 | snp | C/T | 0.000182196 | 0.00954279 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869199 | GTGACAGAACTGGGT[C/T]TCCCTCTTTTGCAGC | 5336 |
| rs368159365 | snp | A/G | 3.31796e-05 | 0.00407292 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895970 | GACTTAAAGGGGAAG[A/G]CAGCTAGGGTTGGAT | 5336 |
| rs368161088 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913540 | TAAGCTCTTCACTCC[A/G]GAGTCTCTAGCCAGA | 5336 |
| rs368164634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895194 | CTGTATCATTTCCAC[A/G]GGCAGAAAAGGCAGT | 5336 |
| rs368192868 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835852 | CTGGTGACCCTGGGT[A/G]TCCCTTGGCTGGTGG | 5336 |
| rs368219963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816423 | CTGGCATATCCTATT[C/T]TGGGACCATGAAAAG | 5336 |
| rs368220809 | in-del | -/T | 0.468349 | 0.121752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827190 | TAGAGGATTGCTGGG[-/T]TTTTTTTTTTTTTGG | 5336 |
| rs368241065 | snp | A/C/G/T | 9.94347e-05 | 0.00705051 | missense, synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937780 | CATGCAGATGAATCA[A/C/G/T]GCATTGTTTTCTCTC | 5336 |
| rs368242901 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950177 | GCTGAATCCTCCTAT[A/T]AGAAAAGAAATCTAC | 5336 |
| rs368264521 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810086 | AACCTCCTCCTCCTG[A/G]GTTCAAGTGATTCTC | 5336 |
| rs368290525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882413 | GGTGGGGCCTCATGT[A/G]GCTCCCACTCCAGAG | 5336 |
| rs368337142 | snp | C/T | 3.3168e-05 | 0.00407221 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910658 | GACGCACCTGCGCTG[C/T]GCCGAGTTCGAGCTG | 5336 |
| rs368346315 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902702 | CCTCATGACCTAATC[A/C]CCTTCTGTGTTACCC | 5336 |
| rs368391320 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944895 | AAGTTTCGTACAATC[C/T]AGGTGGTGGGTATAC | 5336 |
| rs368394863 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879919 | TCCGATATTTCTTTC[A/G]TCTTCTTGCCTTCGA | 5336 |
| rs368410901 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928690 | GCTGACCTCAGCCCC[A/G]CCCTACACAGGGAGG | 5336 |
| rs368453570 | in-del | -/CAAACAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957316 | AAACAAACAAACAAA[-/CAAACAAA]AAATCCTTTGGCACC | 5336 |
| rs368453849 | snp | C/G | 4.9788e-05 | 0.00498914 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895771 | GGCTGTCAGTGAACA[C/G]ACGTGGTATTGAGGC | 5336 |
| rs368463830 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931115 | ATGTTTGTTTTTTTT[-/T]CCTGCATCTTAAGTG | 5336 |
| rs368482871 | snp | A/G | 1.671e-05 | 0.00289045 | missense | PLCG2 | GRCh38.p7 | 16:81956876 | AGGAGAAATGCAACA[A/G]GAGGTAGGTCAGCCC | 5336 |
| rs368494408 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822856 | TGGAATGATGTGCTT[C/T]AAAGGCAGAGGAAGA | 5336 |
| rs368512992 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877289 | GAAACCCTGTCTCTA[C/G]TAAAAATACAAAAAA | 5336 |
| rs368517722 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841596 | TCTATAGGGTGTATG[G/T]TCTTTTTCCATTTCA | 5336 |
| rs368520478 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778051 | AAAAAAACAAAAAAA[A/C]AAACAAAAAAAACCA | 5336 |
| rs368522061 | snp | A/G | 4.96857e-05 | 0.00498401 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880984 | TGTGTCGTTCGGGGC[A/G]GCTGTGCCGGACCTC | 5336 |
| rs368524158 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803141 | TTTTTTTTTGTGAGA[C/T]GGAATCTCACTCTGT | 5336 |
| rs368525788 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876016 | CTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 5336 |
| rs368530152 | snp | C/T | 4.9736e-05 | 0.00498653 | missense | PLCG2 | GRCh38.p7 | 16:81927158 | ATCTCAACTGCAGAC[C/T]TCGAGGAGCTAGAAA | 5336 |
| rs368534849 | snp | A/G | 4.97022e-05 | 0.00498484 | missense | PLCG2 | GRCh38.p7 | 16:81891537 | TGACGCGGTGGACAT[A/G]CAGGACATGAACAAC | 5336 |
| rs368535941 | in-del | -/CT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818021 | GTTGTCATCTACTCT[-/CT]GTTCCTTCCTTTCAT | 5336 |
| rs368609883 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809832 | TTTTTTGGCCGGGGC[G/T]GGGGGTGGGGTCAGA | 5336 |
| rs368616874 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789501 | GCTATGTTGCCGAGG[C/G]TGGTCTCCAACTCCT | 5336 |
| rs368617803 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81898044 | ATCAGGCAGATGGAA[G/T]GAGCTGGTATTAACA | 5336 |
| rs368637152 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797651 | CCTGGCTGCCCCTTT[C/T]AGCCTCGGACTTCCG | 5336 |
| rs368648981 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825953 | TGGCATTGGACCAGA[A/G/T]AAATTTTCTCAGATG | 5336 |
| rs368655115 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940892 | AATAGGCCCTTGCTG[C/G]ATGTTGAATTTTCCT | 5336 |
| rs368684142 | snp | A/G | 6.62449e-05 | 0.00575483 | missense | PLCG2 | GRCh38.p7 | 16:81946216 | GGGTACAGCGAGGAC[A/G]TAGAGCTGGCTTCCC | 5336 |
| rs368694820 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801102 | TTTTGCTCGTCTCCA[C/G]AGCTGCAAGATAATC | 5336 |
| rs368698067 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845777 | CAAGGGGTGGAGATG[A/T]CAACAAAAATGCCCA | 5336 |
| rs368707800 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955645 | TTTTCTGGCACATTC[C/T]AAACTTCTTGACTCA | 5336 |
| rs368730794 | in-del | -/ATAG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920044 | AGGAAGAGAGGATAG[-/ATAG]CATGCGCAAAGGTCC | 5336 |
| rs368738612 | snp | C/G | 0.000167746 | 0.00915668 | missense | PLCG2 | GRCh38.p7 | 16:81870881 | CAAAGATGAGCTCAG[C/G]TTTGAACAGTTCCAT | 5336 |
| rs368767352 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864103 | CTAGAGGGCAATTTT[C/G]AAATCTGAGCATGCA | 5336 |
| rs368769675 | snp | A/G | 5.46712e-05 | 0.00522806 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905539 | TCCCGTAGCCACTGC[A/G]GCCACGCCCCTTGCA | 5336 |
| rs368773136 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838249 | CTGCCACCATGCCTG[A/G]CTAATGTTTATATTT | 5336 |
| rs368781393 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906546 | CTTGTGCCTCATCTT[C/T]CCAAGTAACTGGGAC | 5336 |
| rs368785152 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851700 | GTATTCTTACTAGAG[A/C]TGGGGTTTCACCTTG | 5336 |
| rs368785712 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814454 | TCCCAGCACTTGTGG[A/T]GATTGAGGCGGGCAG | 5336 |
| rs368793095 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823586 | GCTGGAGGGCAGTAG[G/T]GTGATCATAGCTCAC | 5336 |
| rs368810846 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869728 | CTGTCAGAGTTGGCT[C/G]TTTTTTCTTCTGTTT | 5336 |
| rs368857343 | in-del | CCCC/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781870 | TCATGTCCTTTCCCC[CCCC/T]CCCCCCGCCCGCCCC | 5336 |
| rs368880019 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899180 | GGCAATGAGTGAAAC[C/T]CCATTTCCAAAAGAA | 5336 |
| rs368887042 | snp | A/G | 1.65886e-05 | 0.00287993 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81927169 | AGACTTCGAGGAGCT[A/G]GAAAAGCAGGTGAGT | 5336 |
| rs368897845 | snp | C/G | 1.65671e-05 | 0.00287807 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81939905 | AGATGATAATGGCCT[C/G]AGCCCTATCTGGGCT | 5336 |
| rs368899387 | snp | A/C/G | 0.000197526 | 0.00993623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908603 | TCTGGTAATGCCCCC[A/C/G]ACCCAGGGAACGCCT | 5336 |
| rs368907385 | snp | A/T | 4.9708e-05 | 0.00498513 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869306 | AGTTTGTGGTAAGTT[A/T]CATGGCTCAGCCTGG | 5336 |
| rs368910187 | snp | C/T | 1.65886e-05 | 0.00287993 | missense | PLCG2 | GRCh38.p7 | 16:81921246 | AGAATGTATGTGGAT[C/T]CCAGTGAAATCAATC | 5336 |
| rs368911948 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956078 | CTCCATCCCCCAGAC[C/G]CCGGTGACCTTTAAC | 5336 |
| rs368933697 | snp | A/C/T | 0.000166121 | 0.00911241 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919640 | CTACCCCGTGACCCC[A/C/T]GAGCTCCTGGAGCGC | 5336 |
| rs368940503 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886132 | GGGGACAAGTAGCCT[C/T]GCATCCTAGAATTCA | 5336 |
| rs368957009 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856237 | TCTGCCATGGGTGTA[C/T]GGACTGATAAAGTAC | 5336 |
| rs368964105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908678 | TCTAGCTCAGGCAGG[A/C]ATTGGGCAGGCTGGG | 5336 |
| rs368974712 | in-del | -/TT | 0.0010452 | 0.0228366 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921369 | AGGGCAAGGGAAGAC[-/TT]TGGAAAACCTGGCCA | 5336 |
| rs368998879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850745 | TGTAACAGCATAGAG[A/C]GCTTCTTCCTGTGTT | 5336 |
| rs369037578 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950904 | ATAAAATAGAACAAA[A/G]GAATAAAAGAGATAG | 5336 |
| rs369037733 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922033 | GCGATGAGAACAGTC[A/G]CCTCTCTAACTGATG | 5336 |
| rs369043484 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931309 | CCCTACTGAATCTAC[C/T]GCATCCCTTGAGTAG | 5336 |
| rs369047353 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953091 | TAAGAAGACACCAGA[A/C]AAAAGTTGCTGGACA | 5336 |
| rs369060306 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921527 | ACCACCTTTGGGCCA[A/C]ATGGCTTCTAATGAA | 5336 |
| rs369064818 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905107 | GGCCAGGCTGGTCTA[C/G]AACTCCTGAGCTCAA | 5336 |
| rs369072495 | snp | C/G | 1.75949e-05 | 0.002966 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956644 | CAGGTTCACATTTTG[C/G]TTTGGAAGGTGTAGT | 5336 |
| rs369077109 | snp | A/G | 0.000132488 | 0.00813795 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937837 | GCCTGAGAGCATGAG[A/G]ACAGAGAAATATGAC | 5336 |
| rs369085057 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914727 | ACATCGCCTTACTCC[A/T]AGTGTTTCTTGCTTT | 5336 |
| rs369089031 | snp | A/C/G | 0.000146993 | 0.00857195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889302 | GCTTGTTGTCGCTTG[A/C/G]GGGTGACTTTTTGAT | 5336 |
| rs369090020 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821010 | GATCCGCCCACCTCA[C/G]CCTCCTGAGTAGCTG | 5336 |
| rs369090249 | snp | A/G | 8.29029e-05 | 0.00643775 | missense | PLCG2 | GRCh38.p7 | 16:81936240 | ATCAGACAGAAGCCC[A/G]TCGACCTCCTGAAGT | 5336 |
| rs369092713 | snp | A/C | 0.000331208 | 0.0128645 | missense | PLCG2 | GRCh38.p7 | 16:81931575 | GCGATCCTCCGGTGG[A/C]GTTTGCCACAGACAG | 5336 |
| rs369094411 | snp | A/T | 0.000544014 | 0.0164837 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859072 | CTTGTGCTATTTTCT[A/T]ATTTTCTCTTTCTCT | 5336 |
| rs369098550 | snp | A/G | 0.000588844 | 0.0171486 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81905423 | GAAGCTGGGCCCCCG[A/G]GGCGATGTGGATGTC | 5336 |
| rs369106789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954223 | TAACAGGGTCCCGCT[A/G]TGTTGCCCAGGCTGG | 5336 |
| rs369124040 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901603 | AAAAAAATTACATCT[G/T]TATTTGTTTAACCTG | 5336 |
| rs369139882 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943662 | TCTGCATTTTAACAA[C/G]ATTCACAGGTGATTC | 5336 |
| rs369150321 | snp | C/T | 0.000115941 | 0.00761296 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895826 | CTGCTGGGACGGGCC[C/T]GATGGGAAGCCGGTC | 5336 |
| rs369154432 | in-del | -/TTTTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785508 | TTCATTTTTTTTTTT[-/TTTTT]GTTCTTAATTTTGCT | 5336 |
| rs369167633 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802416 | CGCGCCCGGCCTCAG[A/G]TGGGTACAGTCTTAT | 5336 |
| rs369216572 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803592 | CTTTCCTTTCTTTTC[C/T]TTTCTCCTTTTCTTT | 5336 |
| rs369217810 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914747 | TTTCTTGCTTTTGAC[C/G]TGTTCCTGCTTATGT | 5336 |
| rs369259797 | snp | C/G/T | 6.62409e-05 | 0.00575471 | missense | PLCG2 | GRCh38.p7 | 16:81939958 | TTGAAATTTATGACC[C/G/T]AAACCTGGCATTTCT | 5336 |
| rs369266271 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918422 | TCTTTCGAAATTGCT[A/G]TTATTTCTATATAGG | 5336 |
| rs369267913 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780793 | GCACTTTGGGAGGCC[G/T]AGCTGGGCTGATCAC | 5336 |
| rs369281824 | snp | A/G | 6.71028e-05 | 0.00579197 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81900747 | TGACCAGCTGCCCTC[A/G]CCCAGCCAGCTGCGG | 5336 |
| rs369293805 | snp | C/G | 0.000163987 | 0.00905353 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854401 | GCATCCTCAGGTGGA[C/G]GGAACTCCAGCTTCT | 5336 |
| rs369296271 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939002 | TGGGGGATTTTGCAA[C/T]GCTCTTTAGTTGTCC | 5336 |
| rs369314687 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848448 | AGAATGGCTGTTAGA[A/G]TTTCATTCTTTCTTT | 5336 |
| rs369329965 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839180 | ATCACTCTTAACATA[C/T]ATCAGTTCAGGTGAA | 5336 |
| rs369333200 | snp | G/T | 3.32038e-05 | 0.00407441 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936391 | CAGGTAAAGGCCGAC[G/T]GAAGGTAGTCCCGTC | 5336 |
| rs369334194 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943778 | AAATCACATTGTAGC[A/G]ATAGGGAAAAATAGG | 5336 |
| rs369336417 | snp | C/T | 1.6636e-05 | 0.00288405 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936200 | AGAAATCCGCTCCTT[C/T]GTGGAGACGAAGGCT | 5336 |
| rs369340245 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808656 | CCGCCACCACGCCTG[G/T]CTAATTTTTTCTATT | 5336 |
| rs369341985 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805816 | TGTTATTGTTGTTTT[G/T]TTTTTTAAATAGAGA | 5336 |
| rs369346213 | snp | C/T | 0.000126038 | 0.00793746 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908639 | CTTCTCCATGCCAAC[C/T]GATGAGGCAGGGTGG | 5336 |
| rs369350365 | snp | A/C/T | 9.95345e-05 | 0.00705396 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869336 | GGAATTTTATGAATG[A/C/T]GGAGTGACTTAGCCT | 5336 |
| rs369357700 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884125 | GGAGGCCGAGGCGGG[C/G]GGATCACTTGAAGCC | 5336 |
| rs369383473 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808042 | CTGCGGAGACAGATA[A/T]GCAAACAATATTAGG | 5336 |
| rs369385259 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804617 | GTTCCCTCAGTAGAT[A/G]TTTGTCCAAATGTTG | 5336 |
| rs369412865 | in-del | -/TTTATTTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841205 | GGCCAAAAAGTAAAC[-/TTTATTTA]TTTATTTATTTATTT | 5336 |
| rs369423406 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918563 | AGTTGACTGTAAATG[C/T]ATGGATTTATTTCTT | 5336 |
| rs369426093 | snp | A/C/T | 8.92871e-05 | 0.00668106 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786214 | TGGGGCAGTGTGGCC[A/C/T]GTCCTCTGGGGCCCT | 5336 |
| rs369432078 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816713 | CACTATGTTGTCTAG[A/G]CTGGTCTTAAACTCC | 5336 |
| rs369441257 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838625 | GGGGTGGGGGCAAGG[A/G]GAGGGAGAGCGTTAG | 5336 |
| rs369442363 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815897 | GAAACCCCGTTTTTT[A/G]CTAAAAATACAAAAA | 5336 |
| rs369445776 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825587 | GGCGTGAGCCACCGC[C/G]CCCAGCCCGAGATGC | 5336 |
| rs369501516 | snp | A/G | 1.69784e-05 | 0.00291357 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893685 | CTGCCACTCTCACAC[A/G]GCCACCTGCCTTCTC | 5336 |
| rs369507922 | snp | C/T | 3.32353e-05 | 0.00407634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957916 | CACGCAGCCCATTTC[C/T]CATGGCCCACTGCTG | 5336 |
| rs369514332 | in-del | -/TTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910109 | TTGTTGTTGTTGTTG[-/TTG]AGATGGAGTCTCGCT | 5336 |
| rs369516453 | snp | A/G | 3.31312e-05 | 0.00406995 | missense | PLCG2 | GRCh38.p7 | 16:81919609 | AGCATTCACTCTACC[A/G]AAAGATGAGACTGCG | 5336 |
| rs369529901 | snp | C/G | 0.000170115 | 0.00922109 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923440 | AGCCGCCTCCCTCCC[C/G]TCCTGTCCCTGGCCT | 5336 |
| rs369542249 | snp | A/G | 5.71206e-05 | 0.00534388 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912728 | TCAGGTGGGTGCGAG[A/G]GTGGGAGGCACATGC | 5336 |
| rs369542354 | snp | A/G | 0.000960296 | 0.0218912 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786046 | GAAGAGCCAGATCAA[A/G]AGAGCCCTGGAGCTG | 5336 |
| rs369542682 | snp | A/G | 0.000161987 | 0.00899818 | missense | PLCG2 | GRCh38.p7 | 16:81907695 | TCTAGAAATGGACTC[A/G]GCACTACTGCGCCAT | 5336 |
| rs369555285 | snp | C/T | 0.00152822 | 0.0276002 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81889177 | TCATTTTAAGGAGCA[C/T]TGGGCTCAGGATCTG | 5336 |
| rs369564051 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868919 | ATAAATCTCTTATGT[G/T]ACCTATGTCCCTGGA | 5336 |
| rs369565226 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794089 | AGGACTTGCTCTGCC[A/G]GGTGCTGGAGGTACC | 5336 |
| rs369565626 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81936702 | CTCCAGGCCTGTTGC[G/T]GTGTGAGGGCTTTCT | 5336 |
| rs369567689 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879186 | GGGCCACACACTGGG[A/C]TCCCTCCAGATGTAA | 5336 |
| rs369573580 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836522 | GAGGTGGGTGGATCA[C/G/T]CTGAGGTGAGGAGTT | 5336 |
| rs369576817 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850524 | GGGCTCTCAGTGTGA[C/T]AGAAATTGACAAGAG | 5336 |
| rs369578585 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866694 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGGGCT | 5336 |
| rs369585633 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843083 | ATTTCTGTGGCTGGG[G/T]TATCTCACTTTCTTC | 5336 |
| rs369588165 | in-del | -/TA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899271 | GGAGGAGTATGTGTG[-/TA]TATATATATATATAT | 5336 |
| rs369592389 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810377 | TTTTTCTCTCAGCAT[C/T]TATGCTTGGCCTTCG | 5336 |
| rs369597481 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840939 | CCCTTGGGGATGGGG[A/T]GTCCCAGAGGGGAGA | 5336 |
| rs369608316 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856444 | ACCACTCCTCAATGC[C/T]GCTTATTAACAAGGG | 5336 |
| rs369614892 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861113 | TATTTGGCATGCCAG[A/G]GATTGCATTGAGCTC | 5336 |
| rs369650533 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892878 | TTTGAGACAGAGTCT[C/T]ACTCTGTTGCCCAGG | 5336 |
| rs369652464 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828602 | CTTTTATGAGCTGCA[C/G]TTTTGATCAGCGAGT | 5336 |
| rs369687608 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81928933 | GTTTCCCATGCGTTG[C/T]GAAGGAAAGCTGAGC | 5336 |
| rs369701327 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941452 | GGTGCTTGGATGGCA[C/G]TTTGACAGAACCAAA | 5336 |
| rs369704658 | snp | A/G | 1.66344e-05 | 0.0028839 | missense | PLCG2 | GRCh38.p7 | 16:81931652 | TGGAAGATTGACACC[A/G]AGGTAGGCACCTGCT | 5336 |
| rs369704668 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909221 | AGTCACTCAAATGAT[C/T]TGCAAGTATAGTTGT | 5336 |
| rs369715245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944538 | TGTGTGATCATAGCT[C/T]ATGGCAGCCTCAGAC | 5336 |
| rs369721455 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912579 | CACCTGGTCGTTTTC[C/T]CTGGCCCTGTGCCGC | 5336 |
| rs369721663 | snp | C/G | 3.33233e-05 | 0.00408173 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936414 | GTCCCGTCCCTGCAA[C/G]GTGGCGGTTGCAGTC | 5336 |
| rs369732261 | snp | C/T | 0.000115912 | 0.00761201 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895850 | GCCGGTCATCTACCA[C/T]GGCTGGACGCGGACT | 5336 |
| rs369736034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932087 | AACATAGCAAATCAG[C/T]GAGACCCGGTTCTTT | 5336 |
| rs369748186 | in-del | -/TTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787177 | GCTATTTCCAGGCTT[-/TTG]TTATTATTCGAAGTG | 5336 |
| rs369750333 | snp | A/G | 0.000380867 | 0.0137945 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858386 | CCTGTTGATTTGCGT[A/G]GTTGCTGATTCCTTT | 5336 |
| rs369753322 | snp | A/G | 0.000161987 | 0.00899818 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900805 | CCGGGTGCTGCTGTT[A/G]GCTGTCCAGGGAGCC | 5336 |
| rs369760877 | snp | C/T | 3.31526e-05 | 0.00407127 | missense | PLCG2 | GRCh38.p7 | 16:81919623 | CGAAAGATGAGACTG[C/T]GCTACCCCGTGACCC | 5336 |
| rs369771205 | snp | A/C | 3.31868e-05 | 0.00407336 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854431 | TAATTGGCTCATGTT[A/C]ATTTCATTTTAGTGG | 5336 |
| rs369792925 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871866 | AATGTCTCAATGGAG[A/G]AATTGCTGGGTAAAT | 5336 |
| rs369813220 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892734 | TCATGGAGGTTTGCT[C/G]TGCAGATTATTTTGT | 5336 |
| rs369823486 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826848 | TGCCGGAGACAATTT[-/T]GAGTAATTGCTGGGT | 5336 |
| rs369854644 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816822 | TTATGACTTACTCCC[A/G]AGGTCCTGATGTCCA | 5336 |
| rs369861250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933727 | GAGCTAAGCACCCCC[C/T]AAACAGTCACCATTA | 5336 |
| rs369887689 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841861 | TGGTTTTTCTTAAAG[C/T]AGGGTCCTTGGCTGA | 5336 |
| rs369914884 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933123 | GAAATGAAGCTGAGC[G/T]GTTCAAGGTTGCTGT | 5336 |
| rs369948042 | snp | C/T | 8.93615e-05 | 0.00668377 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934399 | GGGATTTCTCGGGGG[C/T]GGGCACTAAAGACAG | 5336 |
| rs369966847 | snp | C/G | 1.65627e-05 | 0.00287769 | missense | PLCG2 | GRCh38.p7 | 16:81956761 | GAAGAACTGAACAAC[C/G]AGCTCTTTCTGTATG | 5336 |
| rs369980441 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81903333 | GACAAACCCGTCAAC[A/C]GAGAAACACCAAACA | 5336 |
| rs369985669 | in-del | A/CCCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781872 | ATGTCCTTTCCCCCC[A/CCCC]CCCCGCCCGCCCCCG | 5336 |
| rs370001088 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875419 | AGCTGCAGAGCTAGG[A/C]TTTGATTTTCTGCCC | 5336 |
| rs370019979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860902 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 5336 |
| rs370025257 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802727 | CAGGCATGCGCCACC[A/C]CGCCCAGCTGATTTT | 5336 |
| rs370025414 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885634 | TAGAACTTTTTTTTT[A/T]AAAATATAGCCATAA | 5336 |
| rs370035331 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843604 | ATGCCCAATTTTTGG[A/G]TGCTTTGATGAACCC | 5336 |
| rs370042119 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846376 | TAGCTTTATTCTGCT[C/G]GCCATCCCACTCCTG | 5336 |
| rs370051028 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803960 | TGCTGGGATTACAGG[G/T]ATGAGCCACCGTGCC | 5336 |
| rs370063399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868315 | CCACTTCCCCTCCCT[A/G]GCCCTTAGTGACCTT | 5336 |
| rs370075775 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795402 | GCATTCTGGCATAGG[C/G]CATAGCAACAAAGCT | 5336 |
| rs370128364 | snp | A/C | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958987 | CAAATGCAGCCATCT[A/C]CCTTGGGGCAGATCT | 5336 |
| rs370130567 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836872 | GACAGTCATCTCAGC[C/G]TTACATGAGTGCACA | 5336 |
| rs370148064 | snp | G/T | 0.000321948 | 0.0126835 | missense | PLCG2 | GRCh38.p7 | 16:81889226 | ATGACAAAGTTCATT[G/T]ATGACACCATGCGTG | 5336 |
| rs370150416 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852757 | TCTACAATCTGGGCA[C/T]GGGTGGGGACTGGGA | 5336 |
| rs370187601 | snp | A/G | 8.28013e-05 | 0.0064338 | missense | PLCG2 | GRCh38.p7 | 16:81928621 | CTCAATACCTATAAC[A/G]TCGGTACGTGCACAC | 5336 |
| rs370187871 | in-del | -/TAAAAAGGA | | | cds-indel | PLCG2 | GRCh38.p7 | 16:81962222 | AGCAAAAAGGATGGC[-/TAAAAAGGA]CCTCAACCCTTTTGA | 5336 |
| rs370188982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811287 | TAAAGACTAGAGATC[A/G]GGTATGTAAAACCTT | 5336 |
| rs370195947 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900523 | CGCCCGGTTTCTGTC[A/G]TCCCAGGGAGCTGCC | 5336 |
| rs370224976 | snp | A/C | 0.00010531 | 0.00725562 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870817 | TCTTACGGTGGACAT[A/C]AAAAATCATGTGGTC | 5336 |
| rs370232361 | snp | C/T | 3.31989e-05 | 0.00407411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893827 | GGTGGAGGTCAGGCT[C/T]GCAGCAAATTGAGGA | 5336 |
| rs370239426 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899906 | ATGTTGTGACCACAC[A/G]CTCAAAAGGCCCTGA | 5336 |
| rs370242901 | snp | A/G | 6.62954e-05 | 0.00575702 | missense | PLCG2 | GRCh38.p7 | 16:81786138 | TGATCATGGAGACGC[A/G]GCAGGTGGCCTGGAG | 5336 |
| rs370249198 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845771 | TAAGATCAAGGGGTG[G/T]AGATGTCAACAAAAA | 5336 |
| rs370251982 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890942 | CTGAGGCGGGTGGAT[C/T]GCTTGAGGTTAGGAG | 5336 |
| rs370255394 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888651 | GGGAGGCACAGAGAC[A/G]GTATGTAACTTGCCC | 5336 |
| rs370264024 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784978 | TTGAGCAGAGGAGTG[A/C]CATGATTTGATTCAT | 5336 |
| rs370282807 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851800 | TTACAGGCGTGGGCC[A/C]CCAGTGCCCGGCTTG | 5336 |
| rs370287809 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826190 | GCTAGAGTCCTCCTC[A/G]GCCCCTTTGCCACCT | 5336 |
| rs370300419 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952991 | AAGGCAGGTTGAAAT[C/T]ACGTACTTCCTGAGG | 5336 |
| rs370318941 | snp | A/C/G | 7.01107e-05 | 0.0059204 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934410 | GGGGCGGGCACTAAA[A/C/G]ACAGTGAACTCCAAA | 5336 |
| rs370338719 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850791 | GTGTTAAATCCCCAC[C/T]CCTAGGCATGATGTT | 5336 |
| rs370349808 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950441 | TCCTACATATACAAA[C/G]ACAACTGTATAAAGA | 5336 |
| rs370352962 | snp | A/G | 4.96973e-05 | 0.00498459 | missense | PLCG2 | GRCh38.p7 | 16:81786116 | CCCGAGCGGAGAACC[A/G]TCCAGGTGATCATGG | 5336 |
| rs370354416 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910159 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAACCT | 5336 |
| rs370388645 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944230 | TTGATGGGTAGATAA[A/G]TCCATGACAAAACAA | 5336 |
| rs370389641 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851571 | AGGCTGGAGTGCAGT[G/T]GCGTGGTCTCGGCTC | 5336 |
| rs370392747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904586 | CCCGCCACCCTGCCC[A/C]GCCTGTTCCCTCTGG | 5336 |
| rs370406050 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959982 | AACCTGACATATGGC[A/G]GCATAGGAAGCAGAA | 5336 |
| rs370419725 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876508 | TGCTTCTGTGACCCC[C/T]GCCTCTGGCATGGCC | 5336 |
| rs370428551 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867113 | GCCCTTAGAACCAGA[A/G]GAAAGGCTGGAGGTG | 5336 |
| rs370429726 | snp | C/G | 1.65916e-05 | 0.00288019 | missense | PLCG2 | GRCh38.p7 | 16:81908453 | ATTTTGGGGAGAAAT[C/G]GTTCCACAAGAAGGT | 5336 |
| rs370460180 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933281 | GTTCCCACACTGGGC[A/G]CAGCTACCCCTTTTG | 5336 |
| rs370472884 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805405 | TCAGGAGGCTGAGGC[A/G]GGAGAATGGCGTTAA | 5336 |
| rs370477719 | snp | C/T | 0.00178414 | 0.0298142 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905527 | GCCTTGGTCCCTTCC[C/T]GTAGCCACTGCGGCC | 5336 |
| rs370501475 | snp | C/G | 1.66377e-05 | 0.00288419 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854626 | TCTCCTTCCCTGTGC[C/G]TTAGTGTCTTCCTGA | 5336 |
| rs370514761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888436 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCAAACT | 5336 |
| rs370527248 | in-del | -/T/TT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799599 | TGGCCTGTTATTAAT[-/T/TT]TTTTTTTTTTTTTTT | 5336 |
| rs370532346 | snp | C/T | 8.36407e-05 | 0.00646632 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910724 | CGAGTCCAAGCCGTA[C/T]GTGTCTGAGGGTGGA | 5336 |
| rs370539081 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902428 | GGCTGCCGACTTCTA[A/G]TTGTGTCCTCACATG | 5336 |
| rs370547009 | snp | A/G | 0.000413993 | 0.0143814 | missense | PLCG2 | GRCh38.p7 | 16:81956795 | CACACCAGAACTTGC[A/G]CAATGCCAACCGGGA | 5336 |
| rs370566733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888367 | AGGCACCTGCCACCA[C/T]GCCAAGCTGATTTAA | 5336 |
| rs370590867 | snp | C/G/T | 0.000139002 | 0.00833555 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783151 | AGGTGTTATAATGGG[C/G/T]CTTGTGTTTCCTACT | 5336 |
| rs370636314 | in-del | -/GAG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915806 | CCTGCCTGCCCTGAG[-/GAG]CTCTTATAAAAAGTT | 5336 |
| rs370662038 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81873696 | CCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCCT | 5336 |
| rs370666956 | snp | C/G | 0.000165986 | 0.00910855 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946166 | ATTTTCCTCCTTGTT[C/G]TGCTTCAGGATTCAG | 5336 |
| rs370681577 | snp | C/T | 0.000291633 | 0.0120719 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900578 | AGAGGTGTGTGCTCC[C/T]CCTGCCGAGCTGCCC | 5336 |
| rs370683432 | snp | A/G | 1.6574e-05 | 0.00287867 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786139 | GATCATGGAGACGCG[A/G]CAGGTGGCCTGGAGC | 5336 |
| rs370686634 | snp | A/G | 3.67803e-05 | 0.00428821 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907822 | GTCCCCAGGAACCCC[A/G]AGGACCAGCCAGTCC | 5336 |
| rs370693024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899236 | TAAATACATAAATAA[A/G]TGACTTTTCTCCTGC | 5336 |
| rs370697615 | snp | C/T | | | stop-gained | PLCG2 | GRCh38.p7 | 16:81891493 | ACGTACCTGTTTTCA[C/T]GAGAAAACAGCATCT | 5336 |
| rs370718047 | snp | A/T | 1.65754e-05 | 0.00287879 | missense | PLCG2 | GRCh38.p7 | 16:81919504 | GGGGCAAGGTAAAGC[A/T]TTGTCGCATCAACCG | 5336 |
| rs370733999 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885366 | ACAGGATTTCCCCAT[A/G]TTGCTCAGGCTGATC | 5336 |
| rs370736749 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822939 | AGCAGGTTTTCCCTC[C/G]GAGCCTCCAGAAGGA | 5336 |
| rs370736941 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819491 | ACCTCCTGGCTCCTC[A/G]CCCACTGCTTTTCAC | 5336 |
| rs370740090 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784025 | TGCTGCTCTCTGCCC[A/G]CCGTGCCCCCAGTGC | 5336 |
| rs370747068 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947407 | TGCCACTCACAGGTG[C/T]AGCTCGGCATTTCTG | 5336 |
| rs370748826 | snp | C/T | 1.6566e-05 | 0.00287797 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928649 | CACATCATCTTAGCC[C/T]GGATTTCCACCCCTA | 5336 |
| rs370750319 | snp | C/T | 8.3071e-05 | 0.00644427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891431 | AGACACCATCCTGCC[C/T]GTCAACGTGATGATT | 5336 |
| rs370771636 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893849 | AATTGAGGATAACCA[C/T]GTGGTTGCTCCATGT | 5336 |
| rs370810146 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955756 | AAAGTCCCACGGATG[C/T]GTCTAGTTGGCCTTG | 5336 |
| rs370822597 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81937107 | TCAACTTTGCCCTGA[A/G]GAAAACCACTGAAGA | 5336 |
| rs370826636 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925603 | TTAAGATCCAGAAAG[G/T]TCAGCCGGGTGCAGT | 5336 |
| rs370826997 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888394 | TTAAAGAAAAAAAAA[A/T]TGTTTGTATTTTAGT | 5336 |
| rs370840346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847252 | TAGGGCATAGGGTTC[C/T]CATGTTCTCTCTGGG | 5336 |
| rs370847174 | snp | C/T | 0.000961283 | 0.0219025 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81921221 | TATAAACTCCCTCTA[C/T]GACGTCAGCAGAATG | 5336 |
| rs370847504 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81779937 | AGGACACTCGCGATG[C/T]CCGCTCCGCAGCTGT | 5336 |
| rs370850077 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844126 | GGACTACAGGTGCCC[A/G]CCACCACACCCGGCT | 5336 |
| rs370859308 | snp | C/T | 1.80094e-05 | 0.00300073 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905536 | CCTTCCCGTAGCCAC[C/T]GCGGCCACGCCCCTT | 5336 |
| rs370869561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913379 | CTCATCTGATTGAAT[C/G]CTTTGCTACAGCCTG | 5336 |
| rs370877909 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81895118 | GATGTTCATCTTCCA[C/T]ATGACCCATTTCTGT | 5336 |
| rs370878744 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825819 | TCACCAGATTGACCA[A/C]AGCAAGGTCTTGTCC | 5336 |
| rs370887643 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955045 | TTCTTAATAGGGAGG[A/C]AAGTCATTACTAAGT | 5336 |
| rs370920969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906835 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 5336 |
| rs370933608 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878333 | TTCGGGTCCACCCTA[A/C]CCCAGCAAGGCCTCA | 5336 |
| rs370949775 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787871 | ACTCAGCATTTTTCA[-/A]GGTTCATCCACTTTG | 5336 |
| rs370953971 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874558 | TGGCTGGAAGCACAG[A/G]GCAGAGAAAAGTACC | 5336 |
| rs370965344 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913509 | TTCAGATGCAGGCCT[G/T]TCCGTCTCCAAAGCC | 5336 |
| rs370980478 | snp | A/G | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962779 | CAATAATTTAGTCAT[A/G]AGATAGGTAGAGTTA | 5336 |
| rs370987972 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832096 | TCAGTCTTCTCCTTT[A/G]ATAAATGGAGGGGGG | 5336 |
| rs371002403 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871196 | TGGCCATAAGTTTGA[C/T]TGGAATTTGATCTGA | 5336 |
| rs371003200 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814817 | GGGAGTTAACCTCTC[G/T]GAACCTTAGTTTCTT | 5336 |
| rs371069005 | snp | C/T | 0.000555944 | 0.0166632 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81934467 | GAAGAACCAGTCCAT[C/T]GCCATCGAGCTCTCT | 5336 |
| rs371089713 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810027 | AGATGGAGCCTACCT[C/G]TGTCACCAGGCTGGA | 5336 |
| rs371105621 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864909 | TGGTAACTCATTCAG[C/G]GAATAGTTGCCGTCC | 5336 |
| rs371117206 | snp | A/C/T | 0.000153045 | 0.00874649 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908408 | CCCCTCCTCTCTTTG[A/C/T]GGCCCAGGATATACC | 5336 |
| rs371119023 | snp | C/G/T | 0.000101235 | 0.00711396 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870807 | ATGGAGCCATTCTTA[C/G/T]GGTGGACATCAAAAA | 5336 |
| rs371129559 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801070 | TGCCTTGATTTTAGC[C/T]CCATGAGACTCATGA | 5336 |
| rs371143899 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930240 | CCTGGTATATAAGAG[C/T]TCAGAAATCTTAGCT | 5336 |
| rs371145343 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859220 | ATCCTCATTCTATCT[G/T]TAAACCTTCCAAGGG | 5336 |
| rs371168533 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890706 | ATGAGGTCGTTCTCA[C/T]GCAGCAGAAATTAGG | 5336 |
| rs371179755 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837064 | ACTCTAGAATTTATT[A/C]CAGGCCATCCAAGTT | 5336 |
| rs371187923 | in-del | -/GT/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832559 | TGTGTGTGTGTGTGT[-/GT/TG]ATGTATTTTTTGTGG | 5336 |
| rs371199713 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81819584 | GTTATTTATGTATTT[A/T]TTATTATTATTATTT | 5336 |
| rs371210803 | in-del | -/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778071 | AAAAAAAACCAAAAA[-/C]ACACACACACAAAAA | 5336 |
| rs371211804 | snp | C/G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961212 | CTATCATAAAGCTTC[C/G/T]GTTCCCATTGATGTA | 5336 |
| rs371214101 | snp | A/C/T | 4.97305e-05 | 0.0049863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895792 | GTATTGAGGCTGCCG[A/C/T]GTTTCTCCCTGTAGT | 5336 |
| rs371218195 | snp | A/T | 1.65641e-05 | 0.00287781 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931567 | GCAGCAGGGCGATCC[A/T]CCGGTGGAGTTTGCC | 5336 |
| rs371230959 | in-del | -/CTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934805 | CACAGTTCCACGTGG[-/CTG]AGGAGGCCTCACAAT | 5336 |
| rs371233068 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837112 | TTTGAGAACCTTTCT[C/T]TTGCTGTAAAAAGCA | 5336 |
| rs371280238 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809332 | GGCTGGGTGGGGAAT[A/C/T]GGCAGATCAATACCC | 5336 |
| rs371287114 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911783 | GCCTGGCTAATTTTT[G/T]TATTTCCTTTTTTTT | 5336 |
| rs371292526 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922236 | TGCTTCTTATGAAAC[A/G]TCATGCACTATGGCA | 5336 |
| rs371302033 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896128 | GAGAGTGCAAGTTGC[A/T]CCCGGGCTCTAGAGC | 5336 |
| rs371307005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822627 | CTGGGCATGGTGGCG[A/T]GTACCTGTAATCCCA | 5336 |
| rs371319058 | snp | A/G | 0.000232932 | 0.0107894 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889152 | CTTTGCTGATCTCTC[A/G]TTCTCTTTGTCATTT | 5336 |
| rs371326699 | snp | C/T | 0.000282516 | 0.0118819 | missense | PLCG2 | GRCh38.p7 | 16:81936208 | GCTCCTTTGTGGAGA[C/T]GAAGGCTGACAGCAT | 5336 |
| rs371334469 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878542 | TACAGCCCCATTTAT[A/C]TGCCCCCTTTAAAGT | 5336 |
| rs371337965 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899674 | GCTGTTCAAATGGCC[C/T]GAAGCACAGTGGTGA | 5336 |
| rs371341747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803145 | TTTTTGTGAGACGGA[A/G]TCTCACTCTGTCGCC | 5336 |
| rs371354444 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942074 | CGTTCCTAGCCTTGA[C/T]GCTGTAACAGATTTC | 5336 |
| rs371370418 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925284 | AACCGGCTTTTTTGC[A/C]TACTTCCAAACTGGT | 5336 |
| rs371373862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889093 | TTCAGTCTTCGATTG[C/T]GACTGGATGGACCCT | 5336 |
| rs371422608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802238 | TTGCCTCAGCCTCCA[C/T]AGTAGTTGGGATTAC | 5336 |
| rs371432727 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850231 | ATTATCATCAGTTTT[A/G]TTAGGTGTAAGGTTT | 5336 |
| rs371474006 | in-del | -/CTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935253 | TTCCTTGGCCTTCTC[-/CTC]TTCTGCTTCCCTATT | 5336 |
| rs371481625 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892001 | GATGTGGCTGTGAAC[C/T]GGCAGCAGCCATGTC | 5336 |
| rs371485019 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911207 | AAAATGTCCATTTCC[A/G]AGGAGGCCGTATTAC | 5336 |
| rs371489624 | snp | C/T | 3.37285e-05 | 0.00410647 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936160 | GATGACCTTTTTCTC[C/T]GTGTGCAGAAAATCC | 5336 |
| rs371491402 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892558 | AAATTGATTTCACAG[A/T]TCTCTCTTCCCCACC | 5336 |
| rs371502079 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923600 | CCGGGGGCTGGTAAG[A/G]CTGAGTGGAGGCTGG | 5336 |
| rs371508358 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902703 | CTCATGACCTAATCA[C/T]CTTCTGTGTTACCCA | 5336 |
| rs371511092 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877273 | TCCTGGCTGACACGG[C/T]GAAACCCTGTCTCTA | 5336 |
| rs371524184 | snp | A/G | 5.2961e-05 | 0.00514565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786210 | TGGGTGGGGCAGTGT[A/G]GCCCGTCCTCTGGGG | 5336 |
| rs371528206 | snp | A/G | 0.000193981 | 0.00984647 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927030 | GATGAGCAGTAGTGG[A/G]TAATTCATGCCACCT | 5336 |
| rs371535095 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850711 | ATGTAGAAGCGGGGA[A/T]CTTCTGGCACCTGCA | 5336 |
| rs371543332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836125 | CACCAAGGACAAGAC[C/T]AGAGTCATTTTCATC | 5336 |
| rs371544676 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862197 | AGGAGCCACAGAGGC[A/C]GAGGAAAGACTGAAG | 5336 |
| rs371557411 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910372 | CTGGGATTACAGGCA[A/T]GAGCCACTGCGCCCA | 5336 |
| rs371568779 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960086 | AATGGTGCTGGGAAG[A/G]ACCCTCTGCCTAAAA | 5336 |
| rs371591761 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891934 | AAGCAATTCAGTGAC[A/T]CATTGAATTGACTTA | 5336 |
| rs371592140 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934223 | GCACACCAAAACCTC[A/G]TGGAAACAGCTTTGT | 5336 |
| rs371599194 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912000 | GACAGGGTTTCACCG[G/T]GTTAGCCAGGATGAT | 5336 |
| rs371614542 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960990 | TCTTACTGTAGAGCA[G/T]GTCCCAAGGTGTAAA | 5336 |
| rs371620952 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835506 | ATCGCTTAAACCTGG[G/T]AGGTGGAGGTTGCTG | 5336 |
| rs371622211 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912170 | ACTCCTGGCTTCTCG[C/T]GATCCACCTGCCTTG | 5336 |
| rs371633163 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812800 | TCTAGGGTTTTTTAT[A/G]GTTTTAGGTCTTATG | 5336 |
| rs371668324 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878814 | CCTTATCTTGCCTCT[A/C]ACTGTTGGTTCTCTT | 5336 |
| rs371668631 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81917661 | ACATTTTTTACGTAA[C/T]TGTTGGCCATTTATG | 5336 |
| rs371668993 | snp | C/T | 0.000163987 | 0.00905353 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956675 | CACCACATGGTTGTT[C/T]TCTCCCCTGCATCCT | 5336 |
| rs371684034 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930746 | GAGTGCCACCCTGTC[A/T]CAAAAAAAAAAAAAA | 5336 |
| rs371695496 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901131 | TTGTTCATTGGTGAA[C/T]CTTCCCCATCCTCTC | 5336 |
| rs371722107 | snp | A/G | 1.82807e-05 | 0.00302325 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905540 | CCCGTAGCCACTGCG[A/G]CCACGCCCCTTGCAG | 5336 |
| rs371723456 | snp | C/G/T | 0.00014904 | 0.00863121 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858252 | ATTTCTGTTCCCTTT[C/G/T]TCCACTCCAGCTGAC | 5336 |
| rs371756459 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872085 | TGTAACCCCAGCACT[C/T]TGGGAGCCCAGGCGG | 5336 |
| rs371797834 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876883 | AATATTCTGTGATTG[C/G]TGGAATCTCATTTAT | 5336 |
| rs371809997 | in-del | A/TGT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782245 | TGAGATACAAGAAAA[A/TGT]CCTTTAGAAGGACAT | 5336 |
| rs371816221 | snp | A/G | 3.31658e-05 | 0.00407208 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869184 | TTGAAAACCCTCAAG[A/G]TGACAGAACTGGGTC | 5336 |
| rs371818115 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863596 | ATCAGTTGCTGGATT[A/G]CTGTGTATATATCCA | 5336 |
| rs371818178 | snp | C/T | 0.000159987 | 0.00894248 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891456 | ATGATTCGGTCTTCG[C/T]GTTTGACTCTTTTAG | 5336 |
| rs371821710 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823463 | TGCACTGTCTGATCT[C/G]TGAAGTGAGCCCCTT | 5336 |
| rs371827612 | snp | C/T | 0.000238977 | 0.0109285 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897927 | CAATGAAATTATGGA[C/T]GTCTTTTCGCACTTG | 5336 |
| rs371832603 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943442 | AGAACTCACTATCAT[C/G]AGAACAGCAAGTGGG | 5336 |
| rs371845782 | in-del | -/TGTTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893006 | CGAGCCACCATGCCC[-/TGTTT]TGTTTTGTTTTGTTT | 5336 |
| rs371862756 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780706 | TTGGGTAGAGTCAAT[A/G]AAAAGCTGCTGGTGA | 5336 |
| rs371866776 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792445 | GAGATCACTCCACTG[A/C]ACTCCAGCCTGGGTG | 5336 |
| rs371874218 | snp | A/G/T | 0.000140521 | 0.00838118 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956929 | GGGGTCTCTAGGCAC[A/G/T]GTGATGATGGGCACC | 5336 |
| rs371885731 | snp | A/C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81903095 | ACCATCTCCAAATAC[A/C/T]ATTACATTGGGGATT | 5336 |
| rs371887861 | snp | A/C | 0.000232721 | 0.0107845 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957917 | ACGCAGCCCATTTCT[A/C]ATGGCCCACTGCTGA | 5336 |
| rs371898893 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923883 | AAGTGGCAAGCAGTC[G/T]GCTAATTGCTTTCCA | 5336 |
| rs371904990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914456 | CACTTCAATGGGACC[A/G]CGTGAATGAAGAGGT | 5336 |
| rs371905149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829945 | CCTCTCGGTGGCATC[C/T]CCACTAGGTGCCAGG | 5336 |
| rs371920999 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856250 | TACGGACTGATAAAG[C/T]ACCTGGTGCTTAAGG | 5336 |
| rs371935269 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867920 | TAGCCAGGATGGTCT[C/T]GATCCTCTGACCTCG | 5336 |
| rs371948049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933030 | TCTACTTTGCTTAAT[A/G]TGGAAAAGTGTTATT | 5336 |
| rs371992413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826128 | CCTCCAGTTTTCCCC[A/G]TTGTGGTAAGAGATA | 5336 |
| rs371998865 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901108 | AGTGCTAACCTGTTA[C/T]AGTTCATTTGTTCAT | 5336 |
| rs372005523 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859816 | CCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 5336 |
| rs372038487 | in-del | -/CC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781878 | TTTCCCCCCCCCCCC[-/CC]GCCCGCCCCCGAGAC | 5336 |
| rs372042942 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799226 | AAACAACCCCTTAGC[C/T]CCCGCCACCCCCCTA | 5336 |
| rs372045589 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837857 | TGTAGTGCAGTATCA[C/T]AGCCAGGATATTAAC | 5336 |
| rs372053793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803422 | TAAGACTAATATTCC[A/G]TTGCATGGATAGACC | 5336 |
| rs372054297 | snp | A/T | 5.02391e-05 | 0.00501169 | missense | PLCG2 | GRCh38.p7 | 16:81870868 | AAATAGGAGCACACA[A/T]AGATGAGCTCAGCTT | 5336 |
| rs372056789 | snp | G/T | 0.000194019 | 0.00984743 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907637 | CTGGGCTCCACAGTT[G/T]ATGAGGTAGAGGACT | 5336 |
| rs372056935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926382 | TGAAGGAGGGCGTTT[A/G]CATGTCTGGGCACGG | 5336 |
| rs372059140 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889413 | TGGTTAGCTGGGATT[A/G]TTTCTTTTCTTTTCT | 5336 |
| rs372064917 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821036 | AGCTGGGATTACAGG[C/T]GCACACCATCATGCC | 5336 |
| rs372066383 | snp | C/T | 5.37803e-05 | 0.00518529 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921308 | ACATGATTTTGGAGT[C/T]ACGAGGCTGATGTGG | 5336 |
| rs372073917 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81928059 | GATATTCTTCATCTC[A/T]GCCAGACCCTGGGAT | 5336 |
| rs372083518 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907784 | CCCCAGGTAGGGGGA[A/C]ACCCTAGCCACATAG | 5336 |
| rs372085742 | snp | C/G | 4.968e-05 | 0.00498373 | missense | PLCG2 | GRCh38.p7 | 16:81858340 | ATGAATGCGTCCACG[C/G]CCACCATTATCGAGA | 5336 |
| rs372097162 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943409 | CTACACACTTTTATT[A/C]AACAACCCCATCTCG | 5336 |
| rs372099919 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956471 | TTTGCAATAAATCAA[A/C]AGTGTAAAGACCAAG | 5336 |
| rs372102863 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81954006 | ATGGTATAGTATTAA[C/G]ACTTAAATGGGGTTT | 5336 |
| rs372118668 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957241 | GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATCACA | 5336 |
| rs372133273 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884785 | ATTTACTTAAAAAAC[C/T]TCTTGTCTTGCAGAA | 5336 |
| rs372144349 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811488 | TCTTTTTTCTTTTTT[A/T]AGGTATTTCTCCTAG | 5336 |
| rs372156888 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913607 | GCGTCTTTTGTACAC[C/T]GATGTGAAAAACTGA | 5336 |
| rs372169078 | in-del | CC/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781870 | TCATGTCCTTTCCCC[CC/G]CCCCCCCCGCCCGCC | 5336 |
| rs372191274 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851730 | GTTGGCCAGGCTGGT[C/G]TCGAATTCCTGACCT | 5336 |
| rs372210761 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899274 | GGAGTATGTGTGTAT[A/G]TATATATATATATAT | 5336 |
| rs372218870 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796248 | CAGATGTGGCCCTCC[C/T]CTCCCCAGCACAGAC | 5336 |
| rs372223063 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838312 | GGCAGGTTTTGAGCT[C/T]CTGGCCTCATGTGAT | 5336 |
| rs372240617 | snp | A/G | 0.000155988 | 0.00883004 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81900654 | GCACTGCAGCGTGGA[A/G]CAACAGCGTCACATG | 5336 |
| rs372245323 | snp | C/G | 0.000304269 | 0.0123305 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912727 | TTCAGGTGGGTGCGA[C/G]GGTGGGAGGCACATG | 5336 |
| rs372245335 | snp | A/G | 0.000163986 | 0.00905352 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919544 | GCACTTTGTGCTGGG[A/G]ACCTCCGCCTATTTT | 5336 |
| rs372248398 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828408 | ACGCCCGGCTAATTT[G/T]TTTGTATTTTTAGTA | 5336 |
| rs372253185 | snp | C/T | 0.000115939 | 0.00761289 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880992 | TCGGGGCGGCTGTGC[C/T]GGACCTCGGTGCCTG | 5336 |
| rs372264710 | in-del | -/GTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916591 | AACCATTTTTTTTTT[-/GTG]TGTGGTGAGACTTAA | 5336 |
| rs372269946 | snp | A/C/G | 0.000331262 | 0.0128658 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919610 | GCATTCACTCTACCG[A/C/G]AAGATGAGACTGCGC | 5336 |
| rs372274557 | snp | C/G | 1.65949e-05 | 0.00288048 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883234 | CTCTGTTGAATGTGT[C/G]TGTCTCTAACTGCAC | 5336 |
| rs372276511 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827135 | AGGGGATGCCCCTCA[A/G]CGGGATGTGTGGTAA | 5336 |
| rs372280655 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816743 | CTGGGCTAAAGCAGT[A/C]CTCGCATTTCAGCCT | 5336 |
| rs372282607 | snp | A/G | 9.19109e-05 | 0.00677842 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81938908 | CAAGTTCAAGACGAC[A/G]GTTGTGAGTAAGTCA | 5336 |
| rs372283592 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783639 | TCCGCTGCCGTATTT[C/G/T]CCATTGAGATAAATG | 5336 |
| rs372323490 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789904 | AGGCGCCGCCCTAGG[C/T]GCTAGAGATACAGCA | 5336 |
| rs372331728 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785921 | ACTAAAATCAGTTCA[C/T]TCTTTAATTCTGCCC | 5336 |
| rs372336406 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906930 | GTAGTCCCAGCTACT[A/C]AGGAGGCTGAGGCAG | 5336 |
| rs372347274 | snp | A/G | 0.0023161 | 0.0339513 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908529 | GGAGACGGGGGGCAA[A/G]GATGGCACCTTCCTG | 5336 |
| rs372356083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886210 | TGGTTGACTTTATTA[C/T]GTGCTTTCCCCAAAC | 5336 |
| rs372364755 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923206 | ACCCTAACCCCAGCG[C/G]TAAACCCTAGCCCCA | 5336 |
| rs372399264 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943249 | TTTATAAAGAAAAGA[A/G]GTTTGATTGGCTCAC | 5336 |
| rs372409122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835399 | TCAGGAGTTTGAAAG[C/T]AGCCTGGCCAACATG | 5336 |
| rs372436022 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818011 | GAGAGACCTGGTTGT[C/T]ATCTACTCTCTGTTC | 5336 |
| rs372453515 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828863 | CTTTTTCTTTTCTGA[A/T]TGCCGAGGTGGGTGG | 5336 |
| rs372454426 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820233 | TGTAGACATGTGTAA[C/T]CACCACCCTAATTGA | 5336 |
| rs372457210 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839199 | AGTTCAGGTGAAAAC[A/G]GTGAGTTGATTTAAA | 5336 |
| rs372459195 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953684 | TTGACTAGAGTGGTG[G/T]TTCCTCAAGTCAAGA | 5336 |
| rs372477024 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858438 | TGGGCTACAGGGGGG[-/G]AAAAAAAAAAAAAGG | 5336 |
| rs372482288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825053 | AAAGGCAATGGGTGG[A/G]TTCCCCCTTGGAGCC | 5336 |
| rs372486257 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904686 | GAGTATCAACAGAGC[A/C]CTTACTGTCTGCTAA | 5336 |
| rs372491825 | snp | A/G | 5.13721e-05 | 0.00506788 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81923508 | AACCGTGAAAGCTCT[A/G]TATGACTACAAAGCC | 5336 |
| rs372494175 | snp | A/G | 7.69556e-05 | 0.00620257 | missense | PLCG2 | GRCh38.p7 | 16:81889235 | TTCATTGATGACACC[A/G]TGCGTGAAACTGCTG | 5336 |
| rs372502550 | snp | A/G/T | 0.000132486 | 0.008138 | missense | PLCG2 | GRCh38.p7 | 16:81786077 | GGGACGGTGATGACT[A/G/T]TGTTCAGCTTCCGCA | 5336 |
| rs372504844 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81954318 | TGAGGCACTGCGCCC[A/G]GCGACTTGATTCTTT | 5336 |
| rs372512341 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912870 | CAGCAAAAGCCGCTG[C/T]GAGAATGTGCGCTCC | 5336 |
| rs372517675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914398 | CCCCTCCCTGAGCCA[A/G]GTGGCATGATTCTGA | 5336 |
| rs372535630 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910025 | GGGGTGGGGTGGGGG[-/G]AAGTAGGTAGAATGT | 5336 |
| rs372538067 | snp | A/C | 1.75971e-05 | 0.00296618 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900788 | TCATCAAGGTAGGCA[A/C]CCCGGGTGCTGCTGT | 5336 |
| rs372557475 | snp | A/G | 4.96874e-05 | 0.0049841 | missense | PLCG2 | GRCh38.p7 | 16:81946186 | TCAGGATTCAGGTCC[A/G]TTCCTCTGAAGAATG | 5336 |
| rs372563994 | snp | C/G | 0.000137459 | 0.00828918 | missense | PLCG2 | GRCh38.p7 | 16:81889190 | CATTGGGCTCAGGAT[C/G]TGAACAAAGTCCGTG | 5336 |
| rs372573745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904293 | TACTGAGACTCTGAT[C/G]ATGACTCAGCCAAGG | 5336 |
| rs372595591 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805808 | TTTTTTGCTGTTATT[G/T]TTGTTTTGTTTTTTA | 5336 |
| rs372596242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868922 | AATCTCTTATGTGAC[C/T]TATGTCCCTGGACAT | 5336 |
| rs372601952 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811246 | TCAAATGGGCACACC[A/G]GTGGTACCTTCCTCG | 5336 |
| rs372603106 | snp | C/G | 0.000215408 | 0.0103758 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895799 | GGCTGCCGCGTTTCT[C/G]CCTGTAGTGGACTGC | 5336 |
| rs372606303 | snp | C/G/T | 4.96877e-05 | 0.00498415 | missense | PLCG2 | GRCh38.p7 | 16:81939921 | AGCCCTATCTGGGCT[C/G/T]CAACACAGGAGAAGG | 5336 |
| rs372619063 | snp | C/G/T | 4.97148e-05 | 0.00498551 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869314 | GTAAGTTTCATGGCT[C/G/T]AGCCTGGGAATTTTA | 5336 |
| rs372632086 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906635 | CGCCATGTTGGCCAG[C/G]CTGGTCTTGAACTCC | 5336 |
| rs372640955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836923 | GCACACGGGCATGTA[C/T]TCAGTGTTTCTGTGC | 5336 |
| rs372660599 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847570 | AAGGGTGTTAGGGGT[A/T]GTGTGCCAGAAAATG | 5336 |
| rs372669042 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960237 | GATTCTCTCAGGAAA[C/G]GCACACATGGTATGA | 5336 |
| rs372678135 | snp | C/T | 0.000499858 | 0.0158012 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81905459 | GGAGGACAAGAAGGA[C/T]GAACACAAGCAACAG | 5336 |
| rs372679048 | snp | A/C | 9.96661e-05 | 0.00705855 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854618 | TGTGCCTTTCTCCTT[A/C]CCTGTGCCTTAGTGT | 5336 |
| rs372683546 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805783 | TTTTTTTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 5336 |
| rs372688404 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806204 | ATGTGGCTAGTGGCT[A/G]CCATATTGGATAGCA | 5336 |
| rs372690032 | in-del | -/AC | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962749 | ATATTCCCAAATAAA[-/AC]ACACACACACATACA | 5336 |
| rs372714256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864920 | TCAGGGAATAGTTGC[C/T]GTCCTTCTCCAAAGG | 5336 |
| rs372717095 | in-del | -/CGC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805524 | AAAAAAAAAACAAAA[-/CGC]AAGAAAACAACAAAA | 5336 |
| rs372722356 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851801 | TACAGGCGTGGGCCA[A/C]CAGTGCCCGGCTTGT | 5336 |
| rs372722399 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891994 | GCTGGGGATGTGGCT[-/G]GTGAACCGGCAGCAG | 5336 |
| rs372723698 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850792 | TGTTAAATCCCCACC[C/T]CTAGGCATGATGTTT | 5336 |
| rs372726236 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782090 | ATCGTGTTAGCCAGG[A/G]TGGTCTTGATCTCCT | 5336 |
| rs372730927 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81938928 | TGAGTAAGTCAGTCA[C/T]CTTGGCCCCTCTGCT | 5336 |
| rs372741594 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836569 | AACATGGTGAAACGC[C/T]ATCTCCAACAAAAAT | 5336 |
| rs372752526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953678 | TTTCTCTTGACTAGA[C/G]TGGTGGTTCCTCAAG | 5336 |
| rs372752960 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868011 | CTGGCCCTCGCTTCC[C/T]GCTTCAGCTGAACCT | 5336 |
| rs372759163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940601 | ACACAAGATCCCTTC[A/C]TGGTATAAGAAGGGT | 5336 |
| rs372782604 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808715 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT | 5336 |
| rs372795428 | snp | C/T | 6.62833e-05 | 0.0057565 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81891549 | CATGCAGGACATGAA[C/T]AACCCCCTGTCTCAT | 5336 |
| rs372801969 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912362 | TGAACCACTGTGCTC[A/G]GCCCAATGTATTATT | 5336 |
| rs372807925 | snp | A/C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935947 | TAATTCTAGCCTAAA[A/C/G]GGTGGTGGGAAAACT | 5336 |
| rs372810330 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794125 | AAAGGAGACTCAGTG[C/G]TCATCCTAGAGGCGC | 5336 |
| rs372810644 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918806 | GATGTTTCTGTCTTG[A/C]TGATAAAAGCTAATA | 5336 |
| rs372812991 | snp | C/T | 8.2826e-05 | 0.00643476 | missense | PLCG2 | GRCh38.p7 | 16:81937854 | CAGAGAAATATGACC[C/T]GATGCCACCCGAGTC | 5336 |
| rs372814853 | snp | C/G/T | 0.000185939 | 0.0096404 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907788 | AGGTAGGGGGACACC[C/G/T]TAGCCACATAGGGAG | 5336 |
| rs372816667 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961737 | TAACTTATATTAAGA[A/G]CCTCCTGGGCTAAAT | 5336 |
| rs372821258 | snp | C/T | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778075 | AAAACCAAAAACACA[C/T]ACACACAAAAAAAAC | 5336 |
| rs372829072 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844121 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACACC | 5336 |
| rs372830469 | snp | A/C/G | 0.000263518 | 0.0114758 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786206 | TCGCTGGGTGGGGCA[A/C/G]TGTGGCCCGTCCTCT | 5336 |
| rs372854680 | in-del | -/AGGTACCCAAAGAGGAGGAAGTGG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835049 | AGTGGGAGGAGGTGG[-/AGGTACCCAAAGAGGAGGAAGTGG]CCTTCCAGGTGCCAC | 5336 |
| rs372876011 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795028 | TCCTGGATGACAACC[G/T]TAGAATGTTCTTAGA | 5336 |
| rs372879639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905035 | TGGGATTACAGGCGC[A/G]TGCCACCATGCCCGG | 5336 |
| rs372901925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950963 | ATAAAAGGATAAAAA[A/G]AATAAAACATTCTGG | 5336 |
| rs372926611 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950273 | GTTACTGGGAAAATT[A/G]GGAAGGAAAAGTTAA | 5336 |
| rs372959612 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946579 | GCATCCAGAAAGGAT[A/G]AGTCTATCTAGGAAG | 5336 |
| rs372962733 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939662 | GGGAGATGGGAGGTG[A/C/G]TCTCCTTCCTCTGCT | 5336 |
| rs372968288 | snp | C/G | 0.000165986 | 0.00910854 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880901 | TTTTGTGTGTGCTTT[C/G]CATTTCAGATTCTCG | 5336 |
| rs372974769 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924918 | CGAAGTCCCTCCACT[A/C/T]GAAGTGGCACAGAGT | 5336 |
| rs372975662 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956977 | AAAGCCCTCTGAGTT[A/G]CTTTCTTCAGAAATC | 5336 |
| rs372978206 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795774 | GTGTGATCACAGCTC[A/C]CTGCAGCCTTGAACT | 5336 |
| rs372990360 | snp | A/G/T | 0.00010696 | 0.00731231 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934400 | GGATTTCTCGGGGGC[A/G/T]GGCACTAAAGACAGT | 5336 |
| rs373013824 | snp | A/G | 3.3123e-05 | 0.00406945 | missense | PLCG2 | GRCh38.p7 | 16:81956774 | ACCAGCTCTTTCTGT[A/G]TGACACACACCAGAA | 5336 |
| rs373027395 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916191 | TGGAAATAAACCACT[A/G]AAGCAGAAGTCTTCT | 5336 |
| rs373053288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932235 | AGGTCTGGAATTGGG[C/T]AGACTGGAGTTTGCA | 5336 |
| rs373077728 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846478 | ACATGCAAAACATTA[A/G]CACTCTGCCTAACAC | 5336 |
| rs373096729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903043 | CAAGGTGAGATTTGG[C/G]TGGGGACACAGCCAA | 5336 |
| rs373110092 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777842 | CCAACATAGTGAAAC[C/T]GCGTCTCTAGTAAAA | 5336 |
| rs373114543 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806358 | TCAGGTAGCTTTAAT[A/T]TCCCACAGAGACTGA | 5336 |
| rs373117489 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859753 | ATGTTCGGCAGGATG[A/G]TCTTGAACTCCTGAC | 5336 |
| rs373126584 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784763 | TACCTTCTTTTATGG[C/G]ACTGGAAATGAGCCC | 5336 |
| rs373135056 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813077 | GTTTTGTTGACCATA[A/G]CCTTGTAGTATAGTT | 5336 |
| rs373135803 | snp | C/G | 0.000163986 | 0.00905352 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919677 | ATGGTAGGTGGTGGA[C/G]TCCCTTGTGATTTGG | 5336 |
| rs373138648 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821448 | TGGGCAGCCTCGGTG[A/G]CTGTTGCCTTCCTCG | 5336 |
| rs373142398 | snp | A/T | 3.31592e-05 | 0.00407167 | missense | PLCG2 | GRCh38.p7 | 16:81883318 | CTGCATGACTTCCAG[A/T]GGTTTCTCATACATG | 5336 |
| rs373151132 | in-del | C/TTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808667 | CCTGGCTAATTTTTT[C/TTG]TATTTTTAGTAGAGA | 5336 |
| rs373154332 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795146 | ACAGGACCCTGAAGA[A/T]CTCTAGAGGATCTTA | 5336 |
| rs373161163 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847095 | TTTGACTGACTGGCT[A/G]TAAATTGGGGTTCCA | 5336 |
| rs373175418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881467 | GATTTCCCAAGTGGG[A/G]AATTTCTGAGATGTT | 5336 |
| rs373178067 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956947 | GATGATGGGCACCAC[A/G]GGCCAGGCTTCTGGA | 5336 |
| rs373190282 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810273 | TTACGGTGTGAGCCA[A/C]CGTGCCCAGCCCATG | 5336 |
| rs373202064 | snp | C/T | 5.41472e-05 | 0.00520295 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934393 | GAAGATGGGATTTCT[C/T]GGGGGCGGGCACTAA | 5336 |
| rs373231841 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869930 | TTCTTAGGAAATGAG[C/G]AACCCTGCATCCAAA | 5336 |
| rs373244336 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951486 | TAGATGGTTTTATAG[C/T]TTAGTTTTGTCTTCA | 5336 |
| rs373262652 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807396 | TGGATCTGAGATCCA[A/C]GTTGCAAAGGAAGAG | 5336 |
| rs373290593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798088 | TGCCTGCATTGGCCT[C/T]CCAAAGTGTTGGGAT | 5336 |
| rs373316349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903228 | GGTGTGGTGGTGTCA[A/G]CACGTGGCATGTACC | 5336 |
| rs373339057 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822632 | CATGGTGGCGTGTAC[C/G]TGTAATCCCAGCTAC | 5336 |
| rs373344892 | snp | A/G | 0.000163987 | 0.00905352 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931594 | TGCCACAGACAGGGT[A/G]GAGGAGCTCTTTGAG | 5336 |
| rs373353043 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914796 | GTTGGTGGTTGGTGA[A/G]TGCTGGCTCAGTGAA | 5336 |
| rs373355638 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939176 | TGACACTAGGTTGGT[C/G]CTCTCTGTGCAACAG | 5336 |
| rs373366141 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926786 | TGAACTTTTGTCTTG[A/T]ATGGTCTCTGACTTC | 5336 |
| rs373377275 | snp | C/T | 8.28027e-05 | 0.00643386 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81940007 | AGAAGATATGTTCAG[C/T]GATCCCAACTTTCTT | 5336 |
| rs373415711 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866884 | GCCCAGCTGTTCCTT[A/G]GACCACTCCCAGGGC | 5336 |
| rs373423564 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915444 | CAGTGAAGCTGAGAC[C/G]TCAGGCTGTGGCCGT | 5336 |
| rs373430247 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906790 | CATGCCTATAATCCT[A/G]GCACCTTGGGAGGCC | 5336 |
| rs373432381 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896993 | TCTATAAAGAGCCAG[A/G]TACAAATGTTTCAGG | 5336 |
| rs373522076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825550 | TCCACCTGCCTCGGT[A/C]TCCCAAAGTGCTGGG | 5336 |
| rs373527417 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927420 | GGAAGGATTTCATTA[G/T]GCAGGAGAATTCCCG | 5336 |
| rs373539123 | snp | C/G | 3.31994e-05 | 0.00407414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869344 | ATGAATGCGGAGTGA[C/G]TTAGCCTCTCTCATG | 5336 |
| rs373547380 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922004 | AACTTTTGTTAGTAG[G/T]GAAGGATGTTTTGGC | 5336 |
| rs373559856 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913783 | CCCCATTCCCTCTGC[A/C]CTGATCCCATCCCCT | 5336 |
| rs373561919 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | PLCG2 | GRCh38.p7 | 16:81937814 | GGGCGCACGGGCTAC[A/G]TTCTGCAGCCTGAGA | 5336 |
| rs373582525 | in-del | AA/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888388 | GCTGATTTAAAGAAA[AA/G]AAAAATGTTTGTATT | 5336 |
| rs373593912 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901611 | TACATCTTTATTTGT[G/T]TAACCTGTACATAAA | 5336 |
| rs373638033 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962234 | GGCTAAAAAGGACCT[A/C]AACCCTTTTGACTTT | 5336 |
| rs373683504 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876656 | TAAATGTGTGCGTGA[A/C]CCAAGAGGCACAGTG | 5336 |
| rs373683613 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81791828 | CCCTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 5336 |
| rs373686679 | snp | A/G | 4.9717e-05 | 0.00498558 | missense | PLCG2 | GRCh38.p7 | 16:81956741 | GCCAGCTGAGGAGGC[A/G]GCAAGAAGAACTGAA | 5336 |
| rs373691615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800646 | TTGATTCCCTATCTT[C/T]GCTATTGTGATACTA | 5336 |
| rs373695738 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784982 | GCAGAGGAGTGACAT[G/T]ATTTGATTCATGTTC | 5336 |
| rs373701719 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802957 | ACATTATCATAATCA[G/T]TTTTAGAATGTTTCA | 5336 |
| rs373713852 | snp | C/T | 0.000183721 | 0.00958262 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936419 | GTCCCTGCAAGGTGG[C/T]GGTTGCAGTCACTCC | 5336 |
| rs373714458 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876021 | CTTTTTCTTTCTTTT[A/T]TTTTTTTTTTTTTTT | 5336 |
| rs373729993 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803150 | GTGAGACGGAATCTC[A/C]CTCTGTCGCCCAGGC | 5336 |
| rs373748512 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904604 | CTGTTCCCTCTGGAC[A/T]GCGGCCTGCCTTTCC | 5336 |
| rs373752237 | snp | A/G | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81912687 | GATCCGGAAGCGAGA[A/G]GGGAGCGACTCCTAT | 5336 |
| rs373769668 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820567 | CTCCCCCATTCTCCT[C/T]ATGGGAGATCTTGGG | 5336 |
| rs373771410 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849100 | GCTTAGGCCACGTGG[A/G]GTTGGAGGGGTCATC | 5336 |
| rs373785716 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865938 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs373790253 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829079 | GTATCTGTGATTTTC[A/T]TTCATTAATGGGGTA | 5336 |
| rs373814471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932930 | TCCAGTGTCTCTGAT[A/G]CCACAGTACAGCTCT | 5336 |
| rs373814773 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909906 | GCTCAGACAGCACGG[C/G]TGACCTGCTCCAGGA | 5336 |
| rs373816090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843463 | TTACACAGAGACAAG[C/T]GCTGATGCATTACCA | 5336 |
| rs373822386 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922233 | CATTGCTTCTTATGA[A/T]ACATCATGCACTATG | 5336 |
| rs373839605 | in-del | -/TTATTAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860167 | TTATTATTATTATTA[-/TTATTAT]TTTTTTTTTTTTTTG | 5336 |
| rs373840911 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914246 | GTGAGACAGCTCTGA[C/T]ACAACCGGATCGGGG | 5336 |
| rs373846793 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842335 | CTGATGTGGATGGAG[A/T]TGTGGATATTCACAT | 5336 |
| rs373851681 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851881 | CGGTAAGAACTCAGA[A/C]AGCTTTGAGTGCATC | 5336 |
| rs373852417 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801497 | AGCAATTTCACTCAA[C/T]AGTACAGCACGATAG | 5336 |
| rs373860097 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798850 | GGACTTCAGGGATCC[C/T]ACTGCGTCTTCTCTG | 5336 |
| rs373866566 | snp | C/T | 0.000165986 | 0.00910855 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81928587 | TCCCTTAGGGTCTCT[C/T]TGCAGAGGAATATTG | 5336 |
| rs373867673 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809789 | GTGTCTGATGTCCCA[G/T]TTATTGCTGCCCTCA | 5336 |
| rs373870489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819421 | TGCAGCCAGGCTTGG[A/G]GAAGTCAAGGATTTG | 5336 |
| rs373883495 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884042 | CACAGGGCAGCCCCC[A/C]CTACCCCCCAGCGAA | 5336 |
| rs373883712 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809375 | CCTCAGTCAGGACAC[A/T]CCTGGCTTGTTCTGC | 5336 |
| rs373886813 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890474 | TGATTTTGGAAAGGC[A/C]GTTTCATAGCCCTTT | 5336 |
| rs373910195 | snp | A/G | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908430 | GGATATACCCCCTAC[A/G]GAACTACATTTTGGG | 5336 |
| rs373933998 | snp | A/C/G | 0.000248777 | 0.0111503 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919477 | CCCTGTGTTCTTCCT[A/C/G]CTCCAGGGCTAGGGG | 5336 |
| rs373946027 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913512 | AGATGCAGGCCTGTC[C/T]GTCTCCAAAGCCTAA | 5336 |
| rs373950814 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918431 | ATTGCTATTATTTCT[A/G]TATAGGAATTTATTT | 5336 |
| rs373954501 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904315 | CAGCCAAGGTCACAT[A/G]GCCAGTAAGGTAATA | 5336 |
| rs373962897 | snp | C/T | 0.000132477 | 0.00813761 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81880949 | TCGTCCGTGTTCATC[C/T]TGGGGTGAGGCAGCT | 5336 |
| rs373975933 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882233 | TGGCTCGTGCTGGCC[A/C]AGTGAGGCCCTGTTT | 5336 |
| rs373980906 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910020 | TGGGGTGGGGTGGGG[-/T]GGGGGAAGTAGGTAG | 5336 |
| rs373981873 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955461 | GAGGCAAAACATCCT[C/T]ATCCTCCCCCTGCAT | 5336 |
| rs373992812 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81834614 | CTGCTGCTGCTGCTG[C/T]TGGGAGTTTCAGAGC | 5336 |
| rs374073560 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961028 | AATGTGGATATTTGG[A/G]AAGTGAAAGACTTAT | 5336 |
| rs374096886 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861043 | CGACAAGAAAAAACC[A/T]AAAAAACCAAAACCA | 5336 |
| rs374097370 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809209 | ACACCTCTGCACACC[A/G]CAAGCCACTTGCTGG | 5336 |
| rs374101499 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906518 | CAGACTCCACCTCCC[A/G]GTTGAAGTGATTCTT | 5336 |
| rs374115335 | snp | A/C/G | 6.6275e-05 | 0.00575619 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928666 | GATTTCCACCCCTAT[A/C/G]CCCCATGGGCTGACC | 5336 |
| rs374121323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934625 | GGCAGAGAGTGCATT[C/G]TCTCATTCTTAACTA | 5336 |
| rs374138065 | snp | A/C/T | 6.6368e-05 | 0.00576017 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895770 | GGGCTGTCAGTGAAC[A/C/T]CACGTGGTATTGAGG | 5336 |
| rs374139729 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933758 | TTATCTAAATATTCT[C/G]TCAAGGTCCCCCCTT | 5336 |
| rs374143875 | in-del | -/AAAAACCAAAAACACACACAC | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778059 | AAAAAAAAAAACAAA[-/AAAAACCAAAAACACACACAC]ACAAAAAAAACGCTA | 5336 |
| rs374150535 | snp | A/G | 1.65699e-05 | 0.00287831 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936263 | CCTGAAGTACAATCA[A/G]AAGGGCCTGACCCGC | 5336 |
| rs374154653 | snp | C/G | 4.97484e-05 | 0.00498715 | missense | PLCG2 | GRCh38.p7 | 16:81921214 | AAAGAGATATAAACT[C/G]CCTCTACGACGTCAG | 5336 |
| rs374169830 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820512 | TTTTCCTTTTCTGTT[-/G]GCTGAGCAGCATTCC | 5336 |
| rs374184836 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891705 | CAGGTGGAGGGTGTA[G/T]CACCGCATTCCTTGG | 5336 |
| rs374199208 | in-del | -/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884619 | TGTGTGTGTGTGTGT[-/GT]ACATGTATGCATGTC | 5336 |
| rs374203663 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904457 | TCTTAATCTTGCAGA[C/G/T]GAGAAGCCTGAGGCT | 5336 |
| rs374207215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902606 | TCACTGGAGCTCTAC[C/T]CTCATTCCCACTTAT | 5336 |
| rs374224219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903711 | TAGTTGGTGAGTCTT[C/T]GGGGCAGCCTGGTTG | 5336 |
| rs374229872 | snp | A/G | 0.000166251 | 0.0091158 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880864 | CCGTTTTTGCATTAA[A/G]TGACTTGTCTAAGGT | 5336 |
| rs374233444 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866735 | CCAGCATGAGAGGAC[A/G]CTGGCCTCTCCCTTG | 5336 |
| rs374233612 | snp | A/G/T | 0.000149028 | 0.00863107 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895859 | CTACCATGGCTGGAC[A/G/T]CGGACTACCAAGATC | 5336 |
| rs374235189 | snp | C/T | 4.96882e-05 | 0.00498414 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786052 | CCAGATCAAGAGAGC[C/T]CTGGAGCTGGGGACG | 5336 |
| rs374241975 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781460 | ACTATTGCTTCCGTG[A/G]TTTTCTGTCGTACAT | 5336 |
| rs374246280 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806910 | GAGGAAGCAGGGGTC[A/G]CATGACCCAGGGCTG | 5336 |
| rs374270528 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858702 | AGGACAGATACAGGG[A/T]CTGGAATTTTCCACC | 5336 |
| rs374288353 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934178 | ATCCTGACCTCACCT[A/G]TATTTGAGGGCTGTG | 5336 |
| rs374312954 | snp | A/C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942799 | ACCCCGTGTTCCTCC[A/C/T]CTGCAGGCTGCCCTC | 5336 |
| rs374331040 | snp | C/G | 1.88269e-05 | 0.00306808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900587 | TGCTCCCCCTGCCGA[C/G]CTGCCCACCCTCTTC | 5336 |
| rs374332476 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935709 | TTCCCTCTCCTCCTG[C/T]TCTCCCTTCCCTGCA | 5336 |
| rs374334077 | snp | C/T | 0.000161987 | 0.00899817 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81934470 | GAACCAGTCCATCGC[C/T]ATCGAGCTCTCTGAC | 5336 |
| rs374334218 | snp | A/G | 0.000163987 | 0.00905353 | missense | PLCG2 | GRCh38.p7 | 16:81919512 | GTAAAGCATTGTCGC[A/G]TCAACCGGGACGGCC | 5336 |
| rs374336710 | snp | A/G | 6.62449e-05 | 0.00575483 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880982 | TGTGTGTCGTTCGGG[A/G]CGGCTGTGCCGGACC | 5336 |
| rs374345131 | snp | C/G | 0.000208344 | 0.0102043 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908378 | TGCTGGGGTTTGGTC[C/G]AAGGCTTTCAGAAAC | 5336 |
| rs374351349 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81948443 | TAGTACTGATCCTGG[G/T]TGGACTGGGTTCTGT | 5336 |
| rs374354863 | snp | C/T | 0.000232211 | 0.0107727 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786160 | GGCCTGGAGCAAGAC[C/T]GCTGACAAGATCGAG | 5336 |
| rs374361286 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793972 | AAGACGTATCAGATC[G/T]GTGTGTCATAAACAC | 5336 |
| rs374369194 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835406 | TTTGAAAGCAGCCTG[G/T]CCAACATGGCGAAAC | 5336 |
| rs374370421 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810939 | CTAAGAGGCACCAAG[G/T]GAGGTTATGCACCTG | 5336 |
| rs374370561 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816888 | ATTAGTGGGAAAACA[C/G]TCAGGCACCTGGGGC | 5336 |
| rs374376315 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778361 | GGTGACAGAGTGAGA[A/C]CCTGCCTCTTAGAAA | 5336 |
| rs374386800 | in-del | -/TTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785510 | CATTTTTTTTTTTTT[-/TTT]GTTCTTAATTTTGCT | 5336 |
| rs374390386 | snp | A/G | 0.000133056 | 0.00815539 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81921263 | CAGTGAAATCAATCC[A/G]TCCATGGTACGGTGC | 5336 |
| rs374419817 | snp | C/G/T | 3.32974e-05 | 0.00408017 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910694 | CACGGACCCTGTGCC[C/G/T]AACCCCAACCCCCAC | 5336 |
| rs374427522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828438 | AGAGACTGGGTTTCA[C/T]CATGTTAGCCAGGAT | 5336 |
| rs374430619 | snp | C/G | 1.66059e-05 | 0.00288144 | missense | PLCG2 | GRCh38.p7 | 16:81957986 | AGTCAGCAACAGCAA[C/G]TTTTACTCATAGAAG | 5336 |
| rs374444497 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916701 | GGAGTGCAGGGGCGT[C/G]ATCTTGGCTCACTGC | 5336 |
| rs374449311 | snp | A/G | 8.33629e-05 | 0.00645558 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870808 | TGGAGCCATTCTTAC[A/G]GTGGACATCAAAAAT | 5336 |
| rs374456910 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842494 | GACTGAATAACTGAA[A/G]GTCGGAAAAGAGGTT | 5336 |
| rs374461661 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871595 | GGCCCGCCTCCACTT[C/T]CTAAAGTGCTGGGAT | 5336 |
| rs374465838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805596 | AATTAAAAAGTGGGC[G/T]AAAGATCTGAACAGA | 5336 |
| rs374501993 | snp | C/T | 0.000165634 | 0.00909888 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936341 | CCGCCTCTGGCTGTG[C/T]GGTTCTCAGATGGTG | 5336 |
| rs374508837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922760 | AAACAGGTTTGACAA[C/T]GTCAGAGCTTTTCCC | 5336 |
| rs374517633 | snp | A/C/T | 1.65627e-05 | 0.00287769 | missense | PLCG2 | GRCh38.p7 | 16:81946189 | GGATTCAGGTCCGTT[A/C/T]CTCTGAAGAATGGGT | 5336 |
| rs374554980 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925458 | GAAATGGTGCGGGGG[G/T]GCGTGAAAAGGGCTT | 5336 |
| rs374555323 | snp | C/G/T | 0.000491291 | 0.0156659 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889147 | TCTCACTTTGCTGAT[C/G/T]TCTCGTTCTCTTTGT | 5336 |
| rs374575503 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851782 | CCTCCCAAAGTGCTG[G/T]GATTACAGGCGTGGG | 5336 |
| rs374603262 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962054 | CGTCCCTCCCGAAGC[C/T]GCGCGCTCCGTCGAA | 5336 |
| rs374609450 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867889 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 5336 |
| rs374636399 | snp | A/G | 3.47313e-05 | 0.00416706 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936127 | TAAGAAAATGCACAG[A/G]TGAGACACAGAAGTA | 5336 |
| rs374641731 | snp | C/T | 0.00011608 | 0.0076175 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908487 | GAAGAGGACGAGTGC[C/T]GAGAAGTTGCTGCAG | 5336 |
| rs374662004 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943525 | GGAGATCACAATTCA[A/C]CATGAGATTTGGGTG | 5336 |
| rs374683132 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890386 | GAATAATTAAGGGCA[A/G/T]TTTGGAGGTTAAAGG | 5336 |
| rs374706370 | snp | C/T | 3.31554e-05 | 0.00407144 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895945 | CAGTTGGCTGATTTC[C/T]GGGTGGTGTGACTTA | 5336 |
| rs374711107 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900028 | AATCAACTACAGATA[C/T]ACACAAATGATCTAT | 5336 |
| rs374727335 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888732 | GCTGATGTAACTACT[A/G]TGCCCCCAGGCTGCT | 5336 |
| rs374736333 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930339 | GTCTGGAGAACCCAC[A/G]CCACATTTCTCTCCT | 5336 |
| rs374738167 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907891 | GCAAGGGGATGCTCC[A/G]CTGAAGAAGCTGTTG | 5336 |
| rs374746148 | snp | A/G | 0.000161987 | 0.00899817 | missense | PLCG2 | GRCh38.p7 | 16:81946244 | CCCTCCTGGTTTTCT[A/G]TGAGATGCGGCCAGT | 5336 |
| rs374768937 | snp | C/G | 5.51922e-05 | 0.00525291 | missense | PLCG2 | GRCh38.p7 | 16:81912698 | GAGAGGGGAGCGACT[C/G]CTATGCCATCACCTT | 5336 |
| rs374780126 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961529 | TACAGAGATAGAATT[A/G]AATAACATAAAAATC | 5336 |
| rs374785803 | in-del | -/G | 0.0031567 | 0.0396028 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809682 | TTCTCTGTTCCCTGC[-/G]GTGTGTGAGCCTGTG | 5336 |
| rs374787358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954485 | ATCTAGGTTTTAAGT[A/C]CCACATGCATTCCCC | 5336 |
| rs374791192 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941424 | ATCTGCATCTTTAGG[C/G]AGCTCCCCAGATGGT | 5336 |
| rs374815653 | snp | A/C | 0.488302 | 0.0755777 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778079 | CCAAAAACACACACA[A/C]ACAAAAAAAACGCTA | 5336 |
| rs374825895 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805525 | AAAAAAAAACAAAAC[A/G]CAAGAAAACAACAAA | 5336 |
| rs374830707 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911785 | CTGGCTAATTTTTGT[A/T]TTTCCTTTTTTTTTT | 5336 |
| rs374861135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880496 | AGTGACATGCTTATT[A/G]TGGAATACAATGGTT | 5336 |
| rs374877793 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | PLCG2 | GRCh38.p7 | 16:81939952 | TGACATTTGAAATTT[A/G]TGACCCAAACCTGGC | 5336 |
| rs374887023 | snp | G/T | 6.63152e-05 | 0.00575788 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928507 | GGAAACGGGTTTTCT[G/T]TTTATTATTCCCGTT | 5336 |
| rs374888208 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850968 | CCCTTTGAACAAGAT[G/T]TATAGTGCAAGGTCT | 5336 |
| rs374888275 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818108 | GTGAGAATTACAACA[A/C/G]CTACTTTACAGGGCT | 5336 |
| rs374892617 | snp | C/T | 1.72573e-05 | 0.00293741 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893673 | CAACCCCTGTGGCTG[C/T]CACTCTCACACGGCC | 5336 |
| rs374894568 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808815 | TGCAATCTTGAGCAA[A/G]CTCCATAGCCTCTGT | 5336 |
| rs374895967 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846692 | ATATTTTCAAGATAT[C/G]AGTTCTTCCTGGCTT | 5336 |
| rs374898208 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889765 | GTTCAAGTGATTCTC[A/G]TGCCTCAGCCTCCCG | 5336 |
| rs374901017 | snp | A/G | | | missense | PLCG2 | GRCh38.p7 | 16:81938883 | TCTGTGGAGCCGAGT[A/G]TGACAACAACAAGTT | 5336 |
| rs374905431 | snp | C/T | 8.28096e-05 | 0.00643412 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928628 | CCTATAACGTCGGTA[C/T]GTGCACACATCATCT | 5336 |
| rs374911702 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805811 | TTTGCTGTTATTGTT[G/T]TTTTGTTTTTTAAAT | 5336 |
| rs374913248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942977 | ATGGGACTTGGGCAG[C/T]GAGAGAAGGTACATA | 5336 |
| rs374918968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808646 | CTACAGGTGCCCGCC[A/G]CCACGCCTGGCTAAT | 5336 |
| rs374922699 | snp | A/C | 3.37223e-05 | 0.00410609 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907786 | CCAGGTAGGGGGACA[A/C]CCTAGCCACATAGGG | 5336 |
| rs374923896 | snp | A/G | 4.98087e-05 | 0.00499017 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893828 | GTGGAGGTCAGGCTC[A/G]CAGCAAATTGAGGAT | 5336 |
| rs374925784 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838827 | AATAACATAGATGTG[C/G]TAAAATGCACACATG | 5336 |
| rs374927413 | snp | C/T | 0.000350423 | 0.0132321 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910709 | CAACCCCAACCCCCA[C/T]GAGTCCAAGCCGTAC | 5336 |
| rs374930194 | snp | C/T | 0.000159987 | 0.00894248 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81858264 | TTTCTCCACTCCAGC[C/T]GACTCTAAAGAGGAT | 5336 |
| rs374937188 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81924361 | ATCTGAATAGCAGCA[C/T]GCATGGAGTGCTTCT | 5336 |
| rs374965052 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828550 | GCCGAGAAGCGTCAT[G/T]TTTATTCTGTGCTGT | 5336 |
| rs374965315 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870668 | TGTAGAAAAGCCATG[C/T]TAAATAGCATGACTT | 5336 |
| rs374967208 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925635 | ACTTGCGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 5336 |
| rs374976119 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800429 | GTCCATGTGTTCTCA[G/T]TGATCAGCTCCCACT | 5336 |
| rs374977911 | snp | A/G | 0.000118208 | 0.00768701 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910753 | GAGCAGGAGGCAGGC[A/G]GTGGTCGGGTTAGCT | 5336 |
| rs374983573 | snp | C/T | 0.000167986 | 0.00916322 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81870914 | CTTCTATAAAAAACT[C/T]ATGTTTGAACAGCAA | 5336 |
| rs375002722 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849791 | AAAAAAAAAAAAAAA[A/C]AAAAAACCAAAAAAA | 5336 |
| rs375002897 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905301 | CAGCAAGAACAGGCA[A/G]TGCAAAGGCCCTGCC | 5336 |
| rs375014210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830695 | ACACACATATATTTT[A/T]TATATGTATATATAT | 5336 |
| rs375028352 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887221 | GTCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 5336 |
| rs375034650 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877281 | GACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 5336 |
| rs375036884 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902806 | GTTCCATATGGCTGG[G/T]GAGGCCTCACAATCA | 5336 |
| rs375050893 | in-del | -/TAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867427 | GTCAGGTGTGGTCAT[-/TAT]GGGCACACTGGGTTG | 5336 |
| rs375068217 | multinucleotide-polymorphism | CCC/TCG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789706 | ATTATTATAATAAGT[CCC/TCG]CCGGATGGTCTGGTA | 5336 |
| rs375082177 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857015 | TCAGAAGGAATTCAG[A/G]GATCTCATGCAACCA | 5336 |
| rs375093569 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820245 | TAACCACCACCCTAA[A/T]TGAGACACAGAACAC | 5336 |
| rs375115365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867186 | CAGCGGCTGGGCAGT[A/G]ACGCGCTACTTCCTT | 5336 |
| rs375116208 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794455 | TCATCAGAAATAAGA[C/T]GCAACCAATGCCTGA | 5336 |
| rs375123176 | snp | C/T | | | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81785956 | AGCTTCCTGATTTCT[C/T]CCGATTCCTTCCTTC | 5336 |
| rs375123752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825068 | ATTCCCCCTTGGAGC[C/T]TCCAGAAGGAACACA | 5336 |
| rs375124739 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785314 | GGCTAAAACTGAGGC[A/G]CAGAGAGGTCAAGCA | 5336 |
| rs375128499 | snp | C/T | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778940 | AGCTGGGATGACAGG[C/T]GTGAGCCCGGGCGCC | 5336 |
| rs375154673 | snp | C/T | 1.76275e-05 | 0.00296874 | missense | PLCG2 | GRCh38.p7 | 16:81938804 | TTGGTGTCCCAGGTT[C/T]TCGGTGCTCGCCATC | 5336 |
| rs375172370 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900114 | TATGCATGCACACAT[A/G]CAAATTACATATGTG | 5336 |
| rs375191034 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945989 | GACCAGTCAGTCATG[A/G]CTGCCGGCCTCTGTC | 5336 |
| rs375195217 | in-del | -/TTGTATTTGGAA | | | cds-indel | PLCG2 | GRCh38.p7 | 16:81962196 | CCACTAAGTGATGAA[-/TTGTATTTGGAA]GCAAAAAGGATGGCT | 5336 |
| rs375195776 | snp | A/C | 1.65847e-05 | 0.0028796 | missense | PLCG2 | GRCh38.p7 | 16:81908460 | GGAGAAATGGTTCCA[A/C]AAGAAGGTGGAGAAG | 5336 |
| rs375200129 | snp | A/G | 0.000163986 | 0.00905352 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919595 | CAGTTACTACGAGAA[A/G]CATTCACTCTACCGA | 5336 |
| rs375214540 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919803 | GATACAAATTGAGCA[C/T]AACAAAGACCCTGCC | 5336 |
| rs375218804 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887124 | GGCAAAGTTGTTTTT[C/T]TTTTTTTTCTTTTGA | 5336 |
| rs375220722 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883801 | GCTTTCCTTAAACAG[A/G]TGATGCCTGGGACAG | 5336 |
| rs375222873 | snp | G/T | 0.000159987 | 0.00894248 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81891480 | CTTTTAGTTCCTCAC[G/T]TACCTGTTTTCACGA | 5336 |
| rs375229942 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877684 | CCTACAAGTGTTCCT[C/T]GGTGTGTAGATGGCA | 5336 |
| rs375238611 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956510 | AAACTGCTTGCTTCC[C/G]ACACAATAAATAATT | 5336 |
| rs375240946 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850304 | TAAGTATTTTGGGGT[A/G]CAACATCATGAAGTC | 5336 |
| rs375246761 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829967 | GGTGCCAGGCACTTT[C/G/T]CTGCTGTGGACCCAT | 5336 |
| rs375251083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842956 | GACTCAGTGTGTGGG[G/T]GTTTGTTTGCAGGGG | 5336 |
| rs375258389 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808040 | TGCTGCGGAGACAGA[C/T]ATGCAAACAATATTA | 5336 |
| rs375262734 | snp | A/G | 4.98351e-05 | 0.0049915 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891432 | GACACCATCCTGCCC[A/G]TCAACGTGATGATTC | 5336 |
| rs375280800 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876558 | TAACTTCTCCTGGGG[A/C]CCGACTCAGAGATGA | 5336 |
| rs375287882 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855862 | TAGGAAATGAGGAGC[A/G]AATGTCTGACTGATG | 5336 |
| rs375288497 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863535 | AATCTGTTTGAGTCT[C/T]TGCTTTAAATTCCTC | 5336 |
| rs375293728 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797205 | CCTGACAAGTCAGTG[C/G]AGGTCCAACGTCTTA | 5336 |
| rs375306309 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837493 | CGGAGCCCAGAGGTG[G/T]CTGGTAGAATCCCCT | 5336 |
| rs375321527 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780593 | GATGTTTAAGTCACC[G/T]AATGATGCAGCTGCC | 5336 |
| rs375329212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885425 | TGTCTCAGCTCCCCA[A/G]ATTGCTGGGATTACA | 5336 |
| rs375339276 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840557 | GATGGGAGACAGTGA[C/G]AGATCATCAGGCATT | 5336 |
| rs375348225 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940453 | GGAGAGACCTTTGGC[A/G/T]TCTTGGGGGGGGAGT | 5336 |
| rs375351011 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811450 | CTAGGCTGGGAACTG[C/G]TTTCAGGATGATGTT | 5336 |
| rs375357192 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792512 | AAAAAAAAAAAAAAA[A/G]ACAAAACAAAACAAA | 5336 |
| rs375362338 | snp | C/T | 0.000112437 | 0.00749707 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912592 | TCCCTGGCCCTGTGC[C/T]GCAGGTGGTACTATG | 5336 |
| rs375364337 | snp | G/T | 0.000165986 | 0.00910854 | missense | PLCG2 | GRCh38.p7 | 16:81931539 | AGTCCTTTGTCTTCA[G/T]CCTGGAGCCCAAGCA | 5336 |
| rs375368103 | snp | A/T | 1.67511e-05 | 0.00289401 | missense | PLCG2 | GRCh38.p7 | 16:81870869 | AATAGGAGCACACAA[A/T]GATGAGCTCAGCTTT | 5336 |
| rs375379804 | snp | C/T | 4.97187e-05 | 0.00498567 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931621 | TGAGTGGTTTCAGAG[C/T]ATCCGAGAGATCACC | 5336 |
| rs375396335 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932953 | ACAGCTCTGAGGCAC[-/A]GGGAGGTGCCACGAC | 5336 |
| rs375427173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865549 | TCCTGGGTTTTCTCC[A/G]CTTGTTCTTGAGCAG | 5336 |
| rs375438932 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81936125 | ATTAAGAAAATGCAC[A/G]GATGAGACACAGAAG | 5336 |
| rs375439405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788442 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 5336 |
| rs375454145 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899303 | ATACACACACACACA[C/T]ATAAATATATATGTG | 5336 |
| rs375460772 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910206 | AGTGATTCTCTTGCC[C/T]CAGCCTCCCAAGTAG | 5336 |
| rs375474557 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930747 | AGTGCCACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 5336 |
| rs375485033 | snp | C/T | 3.31219e-05 | 0.00406938 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858249 | AGCATTTCTGTTCCC[C/T]TTCTCCACTCCAGCT | 5336 |
| rs375485035 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872900 | TCATTAATTGCTTTC[C/T]GCATGCAGAGCTGTG | 5336 |
| rs375485784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810076 | AGCTCACTGCAACCT[C/T]CTCCTCCTGGGTTCA | 5336 |
| rs375500279 | in-del | -/GA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781096 | GCAAGAACACAAAGA[-/GA]AAAATTTGCCCGTTA | 5336 |
| rs375517959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844101 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5336 |
| rs375523097 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864007 | GTGATTCGGGTTTTA[C/G]TGTTCTGGGCATGGC | 5336 |
| rs375524001 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958841 | AGCTCTCCACAGGCA[A/G]GAGGTCAACTGCTGC | 5336 |
| rs375539050 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866395 | CCAGCATGAGAGGAC[A/G]CTGGCCTCTCCCTTG | 5336 |
| rs375546602 | snp | C/T | 1.79515e-05 | 0.00299591 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908581 | CCCAATGACTACACC[C/T]TGTCCTTCTGGTAAT | 5336 |
| rs375560658 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878329 | TGGATTCGGGTCCAC[C/G]CTAACCCAGCAAGGC | 5336 |
| rs375572020 | in-del | -/ATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892743 | TTTGCTGTGCAGATT[-/ATT]TTGTCACCCAGGCAT | 5336 |
| rs375574135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896650 | AATTCCCCTTCTGTC[C/G]TAATTCCCTCTTTTG | 5336 |
| rs375577536 | snp | A/G | 3.78845e-05 | 0.00435211 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81938914 | CAAGACGACGGTTGT[A/G]AGTAAGTCAGTCACC | 5336 |
| rs375590398 | snp | C/G | 0.000305426 | 0.0123539 | missense | PLCG2 | GRCh38.p7 | 16:81908553 | CTTCCTGGTTCGGGA[C/G]AGCGAGACCTTCCCC | 5336 |
| rs375598204 | snp | C/T | 9.93739e-05 | 0.0070482 | missense | PLCG2 | GRCh38.p7 | 16:81869221 | TTTTGCAGCATCAGT[C/T]TCCGAGAGTTGAAGA | 5336 |
| rs375627027 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869022 | ATGTCCATGGACATT[G/T]CTTGAGCCTTGCTCA | 5336 |
| rs375634421 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825869 | GGAAGACAGAGACAA[G/T]ATGACAAGGCTAAGA | 5336 |
| rs375635714 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863235 | CCCCTGGAAATCACC[A/C]CTCTACTGTCTGTCT | 5336 |
| rs375635726 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81908303 | GGACCAGCTGAGGCT[G/T]GCCTCTCTATGTTAT | 5336 |
| rs375643540 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837555 | CCCCGTGTCGTGGGT[A/G]CCATGGCAAAGCGTT | 5336 |
| rs375649834 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919376 | CTGTTTATTTACCCA[A/C]TTCTCTAAGGCTGGA | 5336 |
| rs375681558 | snp | A/G | 1.7182e-05 | 0.00293099 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937954 | GCCGCCCTCCCTGGG[A/G]GCTGGGCCGATGCTG | 5336 |
| rs375699249 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921968 | TGTGTGTGAAATGCA[C/T]TAAGAGACCTTAGTA | 5336 |
| rs375703615 | snp | A/G | 0.000100702 | 0.00709511 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907779 | AAGTGCCCCAGGTAG[A/G]GGGACACCCTAGCCA | 5336 |
| rs375712788 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793326 | ACCTAGTTGAGCAGT[C/G]TTCAGGTGGGAAGGG | 5336 |
| rs375713675 | snp | A/G | 1.90308e-05 | 0.00308464 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912725 | CCTTCAGGTGGGTGC[A/G]AGGGTGGGAGGCACA | 5336 |
| rs375723730 | snp | C/G/T | 1.70055e-05 | 0.0029159 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859070 | GACTTGTGCTATTTT[C/G/T]TAATTTTCTCTTTCT | 5336 |
| rs375735837 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926689 | AGCCTCCACCGTCAG[C/T]GGTAGAGCTGGAGTT | 5336 |
| rs375755451 | snp | C/T | 4.97121e-05 | 0.00498534 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858213 | GGCTTTGTAAGCAGA[C/T]GTCTTCCCAGGAATT | 5336 |
| rs375781279 | snp | C/T | 6.97776e-05 | 0.00590626 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81923496 | AAAGCCTCAGAGAAC[C/T]GTGAAAGCTCTGTAT | 5336 |
| rs375799164 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953041 | CATTGCTTCTGTGAC[A/C/G]TTCTTGCCAAAACTG | 5336 |
| rs375830382 | snp | A/G | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963182 | CTGCATTAGAAGATG[A/G]GCAAGGAATAGTAAA | 5336 |
| rs375830653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950992 | GGTTTATCAAAAAGG[A/C]CAAATTTTGTTTTGA | 5336 |
| rs375840800 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840849 | GCACGTGGTCCCTTG[C/G]GGGTGGATCCAGCTA | 5336 |
| rs375843170 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840264 | AGCTGCCCACCCTGT[C/G]ATGGCCTGGGTGGAT | 5336 |
| rs375876385 | snp | C/T | 0.000165631 | 0.00909881 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895820 | AGTGGACTGCTGGGA[C/T]GGGCCCGATGGGAAG | 5336 |
| rs375884568 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870829 | CATCAAAAATCATGT[G/T]GTCACTTTTTTCATA | 5336 |
| rs375893772 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862591 | AAATGTGCTACTGGC[C/T]GAGCATGGTGGCTGA | 5336 |
| rs375894871 | snp | C/T | 6.64761e-05 | 0.00576486 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854620 | TGCCTTTCTCCTTCC[C/T]TGTGCCTTAGTGTCT | 5336 |
| rs375894947 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894555 | CTCTCTCACCAAAGG[C/G]TCATGGGTGCATTTG | 5336 |
| rs375897188 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81779722 | GGAAGGTCAGGGGTC[C/G]TGTGGGGGCTGGCGT | 5336 |
| rs375900202 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81873553 | AGTTGCAAATAACAG[-/T]TTTTTTTTTTTTTAA | 5336 |
| rs375929227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843336 | TTTCTCACACCTTTA[C/T]ACTCATACGTGCACA | 5336 |
| rs375944738 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940174 | GGATGGAATCACTGT[-/A]AAACCGATTGGGTGG | 5336 |
| rs375949030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926313 | TGTGGTGTGGTCAGA[G/T]GTGCATTTTGGAGAG | 5336 |
| rs375974370 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836656 | TGAGGCAGGAGAATC[A/G/T]CTTGAACTCAGGAGG | 5336 |
| rs375982273 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851803 | CAGGCGTGGGCCACC[A/T]GTGCCCGGCTTGTTT | 5336 |
| rs375983971 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816627 | GGGACTACAGGCATG[C/T]ACCACCATGCCCAGC | 5336 |
| rs376020897 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802612 | AGTTTCACTCTTGTC[A/G]CCGGGCTGGAGTGCA | 5336 |
| rs376024516 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898023 | CCCTTCTAAGTGCCA[A/C/G]CCTCCATCAGGCAGA | 5336 |
| rs376030995 | snp | A/G | 1.66582e-05 | 0.00288597 | missense | PLCG2 | GRCh38.p7 | 16:81936193 | ACTTCCGAGAAATCC[A/G]CTCCTTTGTGGAGAC | 5336 |
| rs376045693 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879435 | GCGGCTCTTAACCTT[C/T]TGGTGGGACCTACTC | 5336 |
| rs376052873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862908 | CAAAACCAAAAACAA[C/T]GAAAATAAAAACAAT | 5336 |
| rs376061730 | snp | C/G | 1.75329e-05 | 0.00296077 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81923574 | CCTCATCCACAATGT[C/G]TCCAAGGAGCCCGGG | 5336 |
| rs376068378 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959986 | TGACATATGGCGGCA[C/T]AGGAAGCAGAAGCTA | 5336 |
| rs376070393 | snp | A/G | 4.96973e-05 | 0.00498459 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937855 | AGAGAAATATGACCC[A/G]ATGCCACCCGAGTCC | 5336 |
| rs376075686 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852669 | ACTTGTTTCTGTTAT[C/G]TATTGCTATACAACA | 5336 |
| rs376076039 | snp | C/T | 6.76796e-05 | 0.00581681 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907792 | AGGGGGACACCCTAG[C/T]CACATAGGGAGGAGG | 5336 |
| rs376082445 | snp | A/G | 1.66131e-05 | 0.00288206 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891423 | AAACAAGCAGACACC[A/G]TCCTGCCCGTCAACG | 5336 |
| rs376125738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894832 | AAGCTGAGATCGCGC[C/T]GCTGCACGCCAGCCT | 5336 |
| rs376136289 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867798 | CGCCTCCCGAATTCA[C/T]GCCATTCTTCTGCCT | 5336 |
| rs376157326 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807026 | GGCCCCTCGGGCTGC[C/T]CTGGTTGGCTTTCTC | 5336 |
| rs376162757 | snp | A/G | 1.70478e-05 | 0.00291952 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919441 | AAAAATTGTTTGGCC[A/G]CCAGGATCTTGGCAT | 5336 |
| rs376192123 | snp | A/C/G/T | 4.96812e-05 | 0.00498385 | missense | PLCG2 | GRCh38.p7 | 16:81880916 | CCATTTCAGATTCTC[A/C/G/T]ATGAATTCAAAAAGG | 5336 |
| rs376194994 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807444 | CATTTTTTCAGCTTC[A/T]TACAAGGCAGGAAGC | 5336 |
| rs376204006 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941863 | TTTAGTAGAGACGGG[A/G]TTTTGCCATGTTGGT | 5336 |
| rs376208314 | snp | C/G | 1.6582e-05 | 0.00287936 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81921218 | AGATATAAACTCCCT[C/G]TACGACGTCAGCAGA | 5336 |
| rs376216756 | snp | A/G | 6.62745e-05 | 0.00575612 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936266 | GAAGTACAATCAAAA[A/G]GGCCTGACCCGCGTC | 5336 |
| rs376226106 | snp | C/G | 3.39651e-05 | 0.00412085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883389 | AGCTGGCGGGATGCT[C/G]CTGGGGACTAGTCTC | 5336 |
| rs376227209 | in-del | -/TCTTTTTCT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823983 | CTTCCTTCTTTTCCT[-/TCTTTTTCT]GTTTCTTTTTCTTTT | 5336 |
| rs376236254 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864221 | AGAATTTGCATTTCA[A/T]CCAATCCCCAGGTGA | 5336 |
| rs376238851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952916 | ATAGCAGCTTTACAG[C/T]GGATAGACCCTGCAG | 5336 |
| rs376240742 | snp | C/T | 3.40553e-05 | 0.00412632 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956685 | TTGTTCTCTCCCCTG[C/T]ATCCTCCAGGAGAGC | 5336 |
| rs376273832 | in-del | -/GAG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81936939 | TAATAAGTCCCCGTG[-/GAG]GAGGCACATGTAGGT | 5336 |
| rs376295921 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793829 | ATAAAGAGATTGAGT[C/G]TTGGGGAGATGAGAT | 5336 |
| rs376308756 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923909 | TTCCATGCATTGTCT[A/G]ACCAAATCTTCAACC | 5336 |
| rs376315313 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777915 | CCAGCTACTCAGGAG[C/G/T]CTGAGGCAGGAGAAT | 5336 |
| rs376342880 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845561 | TCATCAGTAGCGACA[C/G]TGCTCCTCATGACTT | 5336 |
| rs376353737 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955621 | CTCACTCAGTGGCTG[C/T]TTTCCTCTTTTTCTG | 5336 |
| rs376358183 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956146 | TCATATAAATGGCAT[C/G]GTGTGATTTGTGATC | 5336 |
| rs376376988 | in-del | -/TCAC | 0.00250104 | 0.0352741 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836019 | CAAAGAAGGCCACAT[-/TCAC]ACATACCAGGGACTG | 5336 |
| rs376403279 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887682 | CAGCCCTTCCCATCT[A/G]AGCACACACACATCT | 5336 |
| rs376405037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861525 | CCTGCCTTTCTCTCC[A/G]TCCTCTTCTTCTCAT | 5336 |
| rs376433426 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868732 | TCTGTGGCATTTTGT[A/G]TTGAGATTATCTGGT | 5336 |
| rs376440238 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794440 | CTGCAATGAAGCGTC[A/T]CATCAGAAATAAGAC | 5336 |
| rs376460484 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801195 | CCCCAACCCCGCAAC[C/T]AACTTAGATGAGTTG | 5336 |
| rs376474550 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784187 | GTGTGCAGTAGAGGG[A/C]GGTGGGGGCAAAGGG | 5336 |
| rs376480930 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825721 | GGAAACACACTCCCA[C/T]GTAACCATCTCCTGA | 5336 |
| rs376507077 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81831489 | TGCCACGAAACTGGC[C/G]CTCTCTATTTGTCTC | 5336 |
| rs376517417 | snp | C/T | 3.31329e-05 | 0.00407005 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81927133 | CTTCCCATCCAACTA[C/T]GTCGAGGACATCTCA | 5336 |
| rs376531693 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930721 | CCACTGCACTTCAGC[C/G]TGGGTGACAGAGTGC | 5336 |
| rs376590364 | snp | C/T | 1.72737e-05 | 0.0029388 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934422 | AAAGACAGTGAACTC[C/T]AAACAGGAGAACAAC | 5336 |
| rs376594543 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867249 | ACAGGGAAACTAGGT[A/C/G]GTTTTCTCCTGCAAG | 5336 |
| rs376603523 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929842 | AGGTCCTTTGGGCAG[G/T]GGGGTGCAGGATCCC | 5336 |
| rs376610995 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792693 | GCTGAGTGAAGGGGG[A/G]AGCCTCTTGTAAAAC | 5336 |
| rs376612422 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802313 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 5336 |
| rs376614017 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814179 | ATGTCTTAAGATACA[A/G]CGGAGGGGAATGGTA | 5336 |
| rs376617973 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891767 | TGGGAACACACTTCC[C/G]TTTGTCAGCTGGCAT | 5336 |
| rs376626646 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875676 | TACCTGGCTACGTGA[C/G]TGCTACCCTGCTACC | 5336 |
| rs376636200 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784323 | ATGCTAACTGAGACC[C/G]TGGTAAATGCTGCAG | 5336 |
| rs376660652 | in-del | -/G/GG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940465 | GCATCTTGGGGGGGG[-/G/GG]AGTAACAATCTCGAG | 5336 |
| rs376667295 | snp | C/T | 1.65605e-05 | 0.0028775 | missense | PLCG2 | GRCh38.p7 | 16:81937802 | TTTTCTCTCAATGGG[C/T]GCACGGGCTACGTTC | 5336 |
| rs376669554 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828055 | AGATCATGCCATTGC[A/C]CTCCAGCCTGCGCAA | 5336 |
| rs376675524 | snp | C/G/T | 0.00112732 | 0.0237153 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858405 | GCTGATTCCTTTATT[C/G/T]TGCTGCCTTTAGCCA | 5336 |
| rs376688438 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912213 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 5336 |
| rs376689137 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787535 | CCCAGCCTTGCACTC[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs376725052 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918499 | ACCCTACTTATTTAA[A/C]AGACTGTCCTTTCCC | 5336 |
| rs376731218 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782502 | CTGCCATAGTTGATA[A/G]AGCGTGGAACGCTGG | 5336 |
| rs376732190 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855002 | ATCACTTGAGGTCAG[C/G]AGTTTGAGACCAGCA | 5336 |
| rs376734359 | snp | G/T | 1.65605e-05 | 0.0028775 | missense | PLCG2 | GRCh38.p7 | 16:81939970 | ACCCAAACCTGGCAT[G/T]TCTGCGCTTTGTGGT | 5336 |
| rs376735122 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841771 | GTCATTACATGTTCT[C/T]CTGCTGTGTATCTCA | 5336 |
| rs376743516 | snp | A/G | 0.00184258 | 0.0302967 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910485 | AATGGCCTGGCCTGC[A/G]TTCTCCCAGCACTGA | 5336 |
| rs376743838 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838530 | AACCAAACGCCGCAT[A/G]TTCTCACTCATCAGT | 5336 |
| rs376761430 | snp | C/G | 5.57222e-05 | 0.00527807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870803 | TAGCATGGAGCCATT[C/G]TTACGGTGGACATCA | 5336 |
| rs376780718 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892766 | ACCCAGGCATTAAGC[C/T]TACTTACTACCCATT | 5336 |
| rs376792999 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820800 | AATTTTTGTATTTTT[-/T]AGTAGAGGCAGGGTC | 5336 |
| rs376802133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943674 | CAAGATTCACAGGTG[A/G]TTCACATTTGCATTA | 5336 |
| rs376809876 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81928830 | CTAAAACTGTAAGTG[C/T]TAAAACAAGGTCTCG | 5336 |
| rs376820942 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789287 | TCGCTTACGCGGATG[C/T]GCTCTCTCGCTCTCT | 5336 |
| rs376821237 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802402 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTCAGGT | 5336 |
| rs376849323 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901824 | AGATGTTAATGAAGA[A/G]ACCCATCTTTTAGTG | 5336 |
| rs376870668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859291 | TCCATTGTGATCTGC[A/G]GATGCCATGTTGGGT | 5336 |
| rs376878428 | snp | C/G/T | 5.0088e-05 | 0.00500419 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923636 | TCGGCAGGTGGGCTT[C/G/T]ACTTGTCCCTTCTTG | 5336 |
| rs376879893 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933714 | CCTGTGACGGCTAGA[A/G]CTAAGCACCCCCCAA | 5336 |
| rs376880548 | snp | A/C | 1.65974e-05 | 0.0028807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891444 | CCCGTCAACGTGATG[A/C]TTCGGTCTTCGTGTT | 5336 |
| rs376903479 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818197 | GCCCTCTGTGCCTCA[C/G]TTTCCTCACTGGTGA | 5336 |
| rs376914496 | in-del | -/TC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871855 | GCACCATCTGAATGT[-/TC]CTCAATGGAGGAATT | 5336 |
| rs376920918 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912113 | AATTTTTGTATTTTT[A/G]GTAGAGACAGAGTTT | 5336 |
| rs376940359 | snp | C/G | 0.0002799 | 0.0118267 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921323 | CACGAGGCTGATGTG[C/G]ATTCCATCTTGTTCC | 5336 |
| rs376949064 | snp | A/G | 8.30737e-05 | 0.00644437 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786001 | GACAATGTCCACCAC[A/G]GTCAATGTAGATTCC | 5336 |
| rs376952198 | snp | C/T | 0.000139767 | 0.00835847 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907651 | TGATGAGGTAGAGGA[C/T]TTGGGGGGCACTAAT | 5336 |
| rs376969034 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903663 | GGGGTGGAGGGAGCT[C/T]GGCCATGGAGGGTCC | 5336 |
| rs376975298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892991 | CTGGGACTCCGGGCA[C/T]GAGCCACCATGCCCT | 5336 |
| rs376987476 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912410 | CCCTGGGGTCTTCCA[C/G]TATTCTTTTCACAAA | 5336 |
| rs376989581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799836 | CTGACCTCGTGATCC[G/T]CCCACCTTGGCCTCC | 5336 |
| rs377024196 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882068 | GACCCTGAGTGTTTA[C/G]TAAAGGGAGAAAGCT | 5336 |
| rs377030281 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838809 | TATATATATATATAT[A/G]TAAATAACATAGATG | 5336 |
| rs377042001 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912880 | CGCTGCGAGAATGTG[C/T]GCTCCTGCGTGCCAG | 5336 |
| rs377047674 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910209 | GATTCTCTTGCCTCA[A/G]CCTCCCAAGTAGCTG | 5336 |
| rs377053809 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782161 | AATTACAGTCATAAG[C/G]CACCGTGCCTGGCCC | 5336 |
| rs377058251 | snp | A/G | 0.000155988 | 0.00883003 | missense | PLCG2 | GRCh38.p7 | 16:81854569 | ACTCAGTTCGTCCTC[A/G]GCACGCTCAGCTTGG | 5336 |
| rs377076058 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806165 | TGATTCAGACAGATT[C/G]AATTCTGAGTGTTCA | 5336 |
| rs377084065 | snp | C/G | 1.65999e-05 | 0.00288091 | missense | PLCG2 | GRCh38.p7 | 16:81936218 | GGAGACGAAGGCTGA[C/G]AGCATCATCAGACAG | 5336 |
| rs377088921 | snp | C/T | 1.65974e-05 | 0.0028807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957953 | AAATCTGTTTTATTT[C/T]AGGTTAAGAGAGAAG | 5336 |
| rs377091034 | snp | A/G | 0.000161987 | 0.00899819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900793 | AAGGTAGGCACCCCG[A/G]GTGCTGCTGTTGGCT | 5336 |
| rs377095061 | snp | A/C | 1.65737e-05 | 0.00287864 | missense | PLCG2 | GRCh38.p7 | 16:81919620 | TACCGAAAGATGAGA[A/C]TGCGCTACCCCGTGA | 5336 |
| rs377097143 | snp | G/T | 0.000157987 | 0.00888643 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883245 | GTGTCTGTCTCTAAC[G/T]GCACCCCCTTTCCCC | 5336 |
| rs377098104 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918476 | TTTTTTTAAATCTAG[A/G]TTTCCCAACCCTACT | 5336 |
| rs377104277 | snp | A/C/G/T | 3.3231e-05 | 0.0040761 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854422 | TCCAGCTTCTAATTG[A/C/G/T]CTCATGTTAATTTCA | 5336 |
| rs377123977 | snp | C/G | 0.000163987 | 0.00905353 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936251 | GCCCGTCGACCTCCT[C/G]AAGTACAATCAAAAG | 5336 |
| rs377139581 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953687 | ACTAGAGTGGTGGTT[C/T]CTCAAGTCAAGAGGG | 5336 |
| rs377148354 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863449 | CTTATCTACTTCTCC[A/G]TCGATGGACACTTGA | 5336 |
| rs377156736 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778047 | CAAAAAAAAAACAAA[A/C]AAAAAAACAAAAAAA | 5336 |
| rs377157246 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817229 | TTTAGGCCGAGATCC[G/T]ATGGGAAGAATCCTC | 5336 |
| rs377175739 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878241 | CGCCTGCCTCGGCCT[C/T]ACAAAGTGCTGGGAT | 5336 |
| rs377187250 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854039 | GTCAAGGTCAACCGG[A/C]CAGTTGACCTTTAGG | 5336 |
| rs377206776 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788459 | CTAATTTTTTGTATT[G/T]TTAGTAGAGACGGGG | 5336 |
| rs377216664 | in-del | -/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852017 | CCTTTGCTCACCTCT[-/TG]GGACTTCGTTCTGTC | 5336 |
| rs377220112 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846275 | AGGACCTACTTTTCC[A/C/G]GTGTGATTCATGCTC | 5336 |
| rs377223625 | snp | A/G | 6.63086e-05 | 0.0057576 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919502 | TAGGGGCAAGGTAAA[A/G]CATTGTCGCATCAAC | 5336 |
| rs377226227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904348 | CCCTGAATTCAAATC[C/T]GGATCTGACCCCCTA | 5336 |
| rs377229167 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81873122 | AAATGAAATAGAAAG[A/T]TTGCAGGCTTGGGAG | 5336 |
| rs377231758 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826968 | CCGATGAGATGACTG[A/T]AGATAGGACACTTGA | 5336 |
| rs377233871 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853706 | AATCCCTGATTTATA[C/G]TACATTTTATTGGTT | 5336 |
| rs377247767 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841981 | CAGCCTAGTAGCTAA[A/G]CTCACCTTGGTGGAG | 5336 |
| rs377254323 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803826 | GGCTGGGATTACAGG[C/T]GTGTACCACCACACC | 5336 |
| rs377255549 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827211 | TTTTTTTTGGGGACA[C/G]GGTCTCACTCTGCCA | 5336 |
| rs377274280 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887839 | TTCAGGGCATGGAGA[A/G]GAAAGCAACAGTTAC | 5336 |
| rs377300099 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907947 | GGCTTGTCTCTGATT[G/T]GCTGGCTGCCCCAGG | 5336 |
| rs377301346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904555 | CGGTCGCCTTAGTCT[A/G]ATCCCCATTGGGTCC | 5336 |
| rs377318051 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926288 | TTCTGGAGGCCCTGG[G/T]GAGCCATCATGTGGT | 5336 |
| rs377319437 | in-del | -/CATG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940204 | CTTGGAGAGCAGGTG[-/CATG]TACAGCCTGTCGTGT | 5336 |
| rs377337349 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790519 | GAGAAGGGTGACGTT[G/T]TATCTCAAGAAGAAC | 5336 |
| rs377356167 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812069 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTTGCTC | 5336 |
| rs377376322 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81897614 | GCAATGGCAGGATCT[C/T]GGCTCACTGCAACCT | 5336 |
| rs377396134 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956775 | CCAGCTCTTTCTGTA[C/T]GACACACACCAGAAC | 5336 |
| rs377400495 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803552 | TTCTTTCTTTCCTTT[-/C]CTTTCCTTCCTTTCC | 5336 |
| rs377416343 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955803 | GGAGGTTGTACTGGT[C/G]GGGGAAGTAGAAATC | 5336 |
| rs377452291 | snp | G/T | 0.000584576 | 0.0170864 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859212 | GGATTTCGATCCTCA[G/T]TCTATCTTTAAACCT | 5336 |
| rs377459241 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864961 | TTTCCTAACCCACAG[C/G]CCTAGGTTGAGCTCC | 5336 |
| rs377483892 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830848 | TCTGGATGACTGAGG[G/T]TATATGCAAGTGCAG | 5336 |
| rs377484780 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951487 | AGATGGTTTTATAGC[A/T]TAGTTTTGTCTTCAT | 5336 |
| rs377496176 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803036 | CCCCCATCCCTGGCA[A/G]TGACAAATCTACTTT | 5336 |
| rs377505552 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840088 | ATTATTTGATGGCCC[A/G]TGCTGGGGGTGTTAG | 5336 |
| rs377516557 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822719 | TGAACCGAGTTCATG[C/T]CGCTGCACTCCAGCC | 5336 |
| rs377527136 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810999 | TGATCTAACAGTGGC[C/T]TTCCTGGCCCTAGTG | 5336 |
| rs377529112 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879333 | AAAATCTGCAACACC[A/T]CCCCTTTTTAAAAAG | 5336 |
| rs377532689 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866804 | GGCTCCTCTCCCCAC[A/G]ACCCCTCTCGCTGCC | 5336 |
| rs377538104 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877972 | CCCTCTTTTTTTTTT[-/AA]TTTTTTTTTTTTTTT | 5336 |
| rs377552627 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859769 | TCTTGAACTCCTGAC[C/T]TTGTGATCCGCCCAC | 5336 |
| rs377554334 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905698 | GGGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGT | 5336 |
| rs377564862 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792412 | CTTGAATGTGCAAGG[C/T]GGAGGCTGCAGTGAG | 5336 |
| rs377593433 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947877 | TAGCCTGTATCTAAC[A/G]ACCGTTACCATCTTG | 5336 |
| rs377596869 | snp | A/C | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962304 | AACTTTTTGAACCCA[A/C]CCGTAAAAGCTATCT | 5336 |
| rs377602975 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877941 | TTTCTCTGTGTGCTT[C/T]TCTGTCTCCAAATCT | 5336 |
| rs377624965 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830967 | TCCCAGCTGGTGACA[A/C]CCTTGCTCTTCCTAC | 5336 |
| rs377666602 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922028 | TTTTGGCGATGAGAA[C/T]AGTCACCTCTCTAAC | 5336 |
| rs377698876 | snp | A/C/G | 0.000251376 | 0.0112084 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934394 | AAGATGGGATTTCTC[A/C/G]GGGGCGGGCACTAAA | 5336 |
| rs377700829 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841690 | CTGGATTTAACTCAT[A/G]CCTGCTAGATCCTTC | 5336 |
| rs377701753 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956752 | AGGCGGCAAGAAGAA[C/T]TGAACAACCAGCTCT | 5336 |
| rs377704915 | snp | C/T | 6.6257e-05 | 0.00575535 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880895 | TCTTTTTTTTGTGTG[C/T]GCTTTCCATTTCAGA | 5336 |
| rs377734057 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858590 | TGGAGTGAGTGGTGC[A/G]TTGGACTCGAGATAG | 5336 |
| rs377734549 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825476 | TTTTTTGTATTTTTA[G/T]TAGAGACAGGGTTTC | 5336 |
| rs377741214 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816931 | TGCCTCTTTCTAGCT[G/T]GTCTAGAGTCTTCTC | 5336 |
| rs377749396 | snp | C/G | 0.000163987 | 0.00905352 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81928614 | ATTGGACCTCAATAC[C/G]TATAACGTCGGTACG | 5336 |
| rs377752384 | snp | C/T | 0.000116076 | 0.00761737 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936239 | CATCAGACAGAAGCC[C/T]GTCGACCTCCTGAAG | 5336 |
| rs377753289 | snp | A/G | 0.00018361 | 0.00957974 | missense | PLCG2 | GRCh38.p7 | 16:81910702 | CTGTGCCCAACCCCA[A/G]CCCCCACGAGTCCAA | 5336 |
| rs377755494 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870815 | ATTCTTACGGTGGAC[A/G]TCAAAAATCATGTGG | 5336 |
| rs377755967 | snp | A/G/T | 1.67186e-05 | 0.0028912 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958032 | AAGGGTATTGTGTGT[A/G/T]TGCGCATGTGTGTTT | 5336 |
| rs377757324 | snp | C/T | 8.28919e-05 | 0.00643732 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81893794 | TGTCGCTGCATTGAA[C/T]GTGAGTAGCTCCTTC | 5336 |
| rs386385242 | in-del | -/TC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871857 | ACCATCTGAATGTCT[-/TC]CAATGGAGGAATTGC | 5336 |
| rs386792982 | multinucleotide-polymorphism | CTGTGCG/GTGTGCC | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778237 | AATTAGCCAAGTGTG[CTGTGCG/GTGTGCC]TCTATAGTCCCAGCT | 5336 |
| rs386792983 | in-del | AC/CCCCCCCCG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781872 | ATGTCCTTTCCCCCC[AC/CCCCCCCCG]CCCGCCCCCGAGACG | 5336 |
| rs386792984 | in-del | CCCCGCCC/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781876 | CCTTTCCCCCCCCCC[CCCCGCCC/T]GCCCCCGAGACGGAG | 5336 |
| rs386792985 | multinucleotide-polymorphism | ATAAT/GTAAC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789721 | CCCCCGGATGGTCTG[ATAAT/GTAAC]TAGGCAGGTTTCACA | 5336 |
| rs386792986 | multinucleotide-polymorphism | GA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796843 | TGGTCTCCAGAACTG[GA/TG]AGACAAACTTCTGTT | 5336 |
| rs386792987 | in-del | CCTTC/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803676 | CTCCCTTCCTTCCTT[CCTTC/T]CTTTTCTTTCTTTCT | 5336 |
| rs386792988 | in-del | CGG/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809831 | ATTTTTTGGCCGGGG[CGG/T]GGGGTGGGGTCAGAA | 5336 |
| rs386792989 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812389 | CGTCATTCTAACTGG[CA/TG]TGAGATGGTATCTCA | 5336 |
| rs386792990 | multinucleotide-polymorphism | ATT/GTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813699 | TACCTGAATATATTC[ATT/GTC]GGATGGCCAGGCTGG | 5336 |
| rs386792992 | multinucleotide-polymorphism | CTC/TTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824442 | CATGGCCCCAGCCAC[CTC/TTA]TTTTCTTGTGATTTG | 5336 |
| rs386792993 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827126 | ATAAGACTCAGGGGA[CA/TG]CCCCTCAACGGGATG | 5336 |
| rs386792994 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829257 | GGGATTACATGCACA[CA/TG]CCAACGTGCCCGGCT | 5336 |
| rs386792995 | multinucleotide-polymorphism | AC/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829258 | GGATTACATGCACAC[AC/GT]CAACGTGCCCGGCTA | 5336 |
| rs386792996 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830192 | AGGCATGTTGGCACG[CAT/TAC]CTGTGGTCCCAGCTA | 5336 |
| rs386792997 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832178 | AAAGCCTTTGCTCAG[CA/TG]CCTGACTCATGGTGA | 5336 |
| rs386792998 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833615 | GCTCACTGTACCTTC[CA/TG]CCTCCTAGGATCAAG | 5336 |
| rs386792999 | multinucleotide-polymorphism | ATG/GTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839777 | ACATTTAGGCTGGGC[ATG/GTA]GTGGCTCATGCCTGT | 5336 |
| rs386793000 | multinucleotide-polymorphism | AC/GG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853265 | GAACCTGGGAGGCAG[AC/GG]GTTGCAGTGAGCTGA | 5336 |
| rs386793001 | in-del | AACA/CG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853341 | GTCTCAAAAAAAAAA[AACA/CG]AAACAACAAAAAAAA | 5336 |
| rs386793004 | in-del | AAAC/GGAAAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858437 | CATGGGCTACAGGGG[AAAC/GGAAAAA]AAAAAAAAGGGACAT | 5336 |
| rs386793005 | multinucleotide-polymorphism | CTG/TTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871897 | TATGGTCTATCCATA[CTG/TTA]TGTGACATTATGCAG | 5336 |
| rs386793006 | multinucleotide-polymorphism | ATT/GTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887596 | CTTGCACCCATGCAT[ATT/GTC]ACCAGCCTGCTGGTC | 5336 |
| rs386793007 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894186 | GTAATCCCAGCACTT[CA/TG]GGAGGCTGAAGTGGG | 5336 |
| rs386793008 | multinucleotide-polymorphism | CT/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902594 | CCTCATTCCCATTCA[CT/TG]GGAGCTCTACTCTCA | 5336 |
| rs386793009 | in-del | G/TTGT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904655 | TGGGCACAGGTGGTG[G/TTGT]TGTTTATTCACCGAG | 5336 |
| rs386793010 | multinucleotide-polymorphism | CGG/TGA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905182 | GTGAGCCACTGCGCC[CGG/TGA]CCAGTATGGGCAATT | 5336 |
| rs386793011 | multinucleotide-polymorphism | CGT/GGC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905859 | GAGATGGGATTTAGT[CGT/GGC]GTTGCCCAGGGTGAT | 5336 |
| rs386793012 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916826 | TATTTTTGGTAAAGG[CA/TG]GGGTTTCACCATGTT | 5336 |
| rs386793013 | multinucleotide-polymorphism | AT/GA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921633 | TGCAGTGCAAATGCT[AT/GA]CTCATATTCCCACCC | 5336 |
| rs386793014 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925974 | TAAGATGTGGCTGCT[CA/TG]GATGACTGTGGGGAC | 5336 |
| rs386793015 | multinucleotide-polymorphism | CAT/GAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927415 | GGCTTGGAAGGATTT[CAT/GAA]TATGCAGGAGAATTC | 5336 |
| rs386793016 | multinucleotide-polymorphism | CTG/TTA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947133 | AAACAACCGGAAACA[CTG/TTA]TAAATAATTTAAGTG | 5336 |
| rs397514562 | snp | A/C | | | missense | PLCG2 | GRCh38.p7 | 16:81919549 | TTGTGCTGGGGACCT[A/C]CGCCTATTTTGAGAG | 5336 |
| rs397692620 | in-del | -/C | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935000 | TGGGAGCTACAATTC[-/C]AAGGTGAGATTTGGG | 5336 |
| rs397702841 | in-del | -/A | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892662 | AACTTAAAAAAAAAA[-/A]CTTTTATTTTCAGTT | 5336 |
| rs397704959 | in-del | -/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881823 | TGTTTTTTTTTTTTT[-/T]GTATTTTTGGTAGAG | 5336 |
| rs397710440 | in-del | -/C | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807213 | CCCCATGTCTTGTCC[-/C]AGCGGTGTCCTCCTC | 5336 |
| rs397720406 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858870 | CTTTTTGGGGATTAA[-/A]TGACTATCATCAGAA | 5336 |
| rs397722927 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854105 | CTCTTGTTTTTTTTT[-/T]GGTAGAATAGTCTGT | 5336 |
| rs397726940 | in-del | -/CT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888040 | TTTGGAGCTGAGACT[-/CT]GCAGTTTACAAGCTG | 5336 |
| rs397730129 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833547 | ATCTTTTTTTTTTTT[-/T]GAGTCAGGATTTCAC | 5336 |
| rs397730965 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930763 | AAAAAAAAAAAAAAA[-/AA]GCCATTTAAATTATT | 5336 |
| rs397749848 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868377 | AACCTTTATTTTTTT[-/T]ACTTATTTTTGGGGG | 5336 |
| rs397757475 | in-del | -/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941715 | CCCTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 5336 |
| rs397762589 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885633 | TAGAACTTTTTTTTT[-/T]TAAAATATAGCCATA | 5336 |
| rs397771033 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870775 | TTTCTGAAACAAAAA[-/A]TTATTCTATAAATAG | 5336 |
| rs397788956 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885335 | GCCCCGACTAATTTT[-/T]GTATCTTTAGTAGAA | 5336 |
| rs397807320 | in-del | -/A | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916305 | AAAAAAAGAAAAAAA[-/A]CAACGTTTTTTAAAA | 5336 |
| rs397821720 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926095 | TAAATTAGTGGGGGG[-/G]AAGTTGGGTACCAAG | 5336 |
| rs397829940 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846236 | GCAGGGAGGACAAGA[-/A]GGACTGGCCTCCCTT | 5336 |
| rs397830233 | in-del | -/TG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852018 | CTTTGCTCACCTCTG[-/TG]GACTTCGTTCTGTCC | 5336 |
| rs397830777 | in-del | -/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881257 | ATAGTTTTTTTTTTT[-/T]AATTACAAAAACTAA | 5336 |
| rs397854815 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935437 | CATTTAAAAAAAAAA[-/A]GACCTTCTACCACAT | 5336 |
| rs397855010 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787550 | CTTTTTTTTTTTTTT[-/T]ATAATAGATTGATTG | 5336 |
| rs397855152 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81897563 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCCC | 5336 |
| rs397855172 | in-del | -/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884620 | TGTGTGTGTGTGTGT[-/GT]ACATGTATGCATGTC | 5336 |
| rs397855204 | in-del | -/T/TG/TTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827203 | GGTTTTTTTTTTTTT[-/T/TG/TTG]GGGGACAGGGTCTCA | 5336 |
| rs397855749 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797293 | TTTGAAAAAAAAAAA[-/A]TTATCTCCACTACCT | 5336 |
| rs397855834 | in-del | -/TTTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785509 | TCATTTTTTTTTTTT[-/TTTT]GTTCTTAATTTTGCT | 5336 |
| rs397855987 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888394 | TTAAAGAAAAAAAAA[-/A]TGTTTGTATTTTAGT | 5336 |
| rs397856005 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916145 | TTCCTCTGTTTTTTT[-/T]AGAAGGAATAAATAT | 5336 |
| rs397942533 | in-del | -/GTCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824786 | CCCCCAAAGGTGTCC[-/GTCC]ATGTCCTAATCTTTG | 5336 |
| rs397945424 | in-del | -/GGG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849050 | AGATGCTTGGAGGGG[-/GGG]CCTGTGTGGGTGGTG | 5336 |
| rs397951385 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789854 | CTTTGCCCCCCCTCC[-/C]ATTGCCTCCCCTCTG | 5336 |
| rs397963348 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849652 | GCGGATGCCTGTAAT[-/T]CCCAGCTACTCGGGA | 5336 |
| rs397968926 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816077 | AAAAAAAAAAAAAAA[-/A]TGTGCCTTCACGGAC | 5336 |
| rs397976937 | in-del | -/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958524 | AGTTCAATGTACTTT[-/T]AACTACCACCGGCTG | 5336 |
| rs398030029 | in-del | -/ATATAT | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838803 | ATCTATGTTATTTAC[-/ATATAT]ATATATATATATATA | 5336 |
| rs398030030 | in-del | -/AA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917244 | AATACCATTTGCTTT[-/AA]AAAAAAAAAAAAAAA | 5336 |
| rs398030031 | in-del | -/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920759 | ACAAACCAGTGCCTT[-/C]CCCCTACCCCGCTGA | 5336 |
| rs398030033 | in-del | -/CACA | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951164 | GCAGGGCCCTGTCTC[-/CACA]CACACACACACACAA | 5336 |
| rs398058435 | in-del | -/AGACCCTTTGCTTAGTGAAGC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946906 | TTTGCTTAGTGAAGC[-/AGACCCTTTGCTTAGTGAAGC]TTATCCCTCCCCAGC | 5336 |
| rs398078790 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807212 | TCCCCATGTCTTGTC[-/C]CAGCGGTGTCCTCCT | 5336 |
| rs398100332 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918909 | GTTTCTTTTTTTTTT[-/T]AAAAAAAGTCACTGT | 5336 |
| rs398119554 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816495 | TAATTTTTTTTTTTT[-/T]GAGACACGGTCTCAT | 5336 |
| rs527243241 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892778 | AGCCTACTTACTACC[C/T]ATTAGTTATTTTTCC | 5336 |
| rs527246560 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835305 | AGCTGTTATAATAAT[A/C]ATGAAGATGGCCGGG | 5336 |
| rs527253474 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878729 | TATCTTGTCCACTCA[C/G]CAGCACGTGTCAAAG | 5336 |
| rs527259364 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884038 | ATTGCACAGGGCAGC[A/C]CCCCCTACCCCCCAG | 5336 |
| rs527261901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930706 | GGAGCCAAGATCGCA[C/T]CACTGCACTTCAGCC | 5336 |
| rs527282614 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779644 | CCACTTCCTCACCCC[C/G]GGCCGGCGCCACCTC | 5336 |
| rs527304973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910411 | TGTCTGTTCTAGGAG[C/T]AGAGGGAAGGTTGTG | 5336 |
| rs527309142 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832103 | TCTCCTTTGATAAAT[-/G]GAGGGGGGGAATAGT | 5336 |
| rs527326955 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807228 | CAGCGGTGTCCTCCT[C/G]CTACATCAGGAGAGG | 5336 |
| rs527329427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935020 | TGAGATTTGGGTGGG[A/G]ACACAGCCAAACCAT | 5336 |
| rs527333811 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792864 | GGGGAGAGAGCCAGA[C/G]CATATCAGCCACTTA | 5336 |
| rs527337923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939131 | TGTTTGCCTGCCTGT[A/C]ACTCAAGTCCGGAAT | 5336 |
| rs527343559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939422 | CTGGTAAAAAGTAGC[C/T]CAATGAACAACTCAG | 5336 |
| rs527351993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814456 | CCAGCACTTGTGGAG[A/G]TTGAGGCGGGCAGAT | 5336 |
| rs527379413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887265 | CCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 5336 |
| rs527381794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836680 | CAGGAGGCTGAGGTG[C/T]AGTGAGCTGAGATTG | 5336 |
| rs527388647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953241 | TTGGATGTGGGAACA[A/G]GAAAAGGAGACTGGT | 5336 |
| rs527395083 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780500 | GTCTATGCCAGCCTC[A/G]AGCAGTTTCTCTTGC | 5336 |
| rs527395908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867445 | GGGCACACTGGGTTG[C/G]AGTTTGAGGCTAGCA | 5336 |
| rs527398498 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813955 | TTGATGGGAAGAAGT[C/T]TGTGGCTATCGTGAA | 5336 |
| rs527410412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818015 | GACCTGGTTGTCATC[C/T]ACTCTCTGTTCCTTC | 5336 |
| rs527414199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938700 | AAATTAGGGCTGGCA[C/T]TGAACTCATCCAGTG | 5336 |
| rs527429157 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889664 | TTGTTTGCTTGTGTG[-/T]TTGTTTTTGAGATGG | 5336 |
| rs527434072 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874870 | ATACCTCTAACTAGG[C/T]TGTAATAACAGTATC | 5336 |
| rs527435618 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81783851 | TTTTTTAGCATACTC[C/T]GTTCTGCCTCCTAGC | 5336 |
| rs527445127 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781444 | TTGTATTTCTATTGC[A/G]ACTATTGCTTCCGTG | 5336 |
| rs527452288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952087 | ATACTGACAAAAACC[A/G]TAACACATTTAGGAG | 5336 |
| rs527467208 | snp | G/T | 3.31296e-05 | 0.00406985 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956808 | GCGCAATGCCAACCG[G/T]GATGCCCTGGTTAAA | 5336 |
| rs527479901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826439 | TACCAGTGTGACCTT[C/G]AGGTCAAAGTGCTCG | 5336 |
| rs527487924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927646 | GAGAGCAGCCACTTT[A/C]AGCGTGCTAGCACTC | 5336 |
| rs527512230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852504 | GTTGAGCTTGTGTCT[C/G]TGTGCCAGTCCAGAG | 5336 |
| rs527537083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852248 | TACCAGTAGTCCTGG[C/G]CAAATAAGTCCCAGG | 5336 |
| rs527550695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803729 | CTGTGTCGGTCAGGC[C/G]GGAGGGCAGTGGTGC | 5336 |
| rs527566035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956334 | GGGTTCCACTTTAAG[C/T]GTGCAGCTGCTTAGA | 5336 |
| rs527569435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880729 | GAGGAGGGCTTCTAC[C/G]TTTTGCTTCTTAAGT | 5336 |
| rs527579946 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848951 | ACTGGAAGGGAGAGC[C/T]TGGCACTAACCAGAC | 5336 |
| rs527592698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833747 | ACAGCCAAGGTGAGG[A/G]TGTTGCCTAGGCTGG | 5336 |
| rs527595271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829345 | AACTCCTGACTTCAG[A/G]TGATCTGCCCGCCTC | 5336 |
| rs527609335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842675 | TTCCTGGTGTCAGGG[C/G]TGGGAGGACGTTCCG | 5336 |
| rs527610820 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959968 | CTACCATATCAAAGA[A/T]CCTGACATATGGCGG | 5336 |
| rs527617177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807253 | GAGAGGGAGGTCAGC[C/T]CTGGGACCCAAGAAA | 5336 |
| rs527623077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859684 | GGACTACAGGCACCC[C/G]CCACCATGCCCGGCT | 5336 |
| rs527630219 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902621 | TCTCATTCCCACTTA[A/T]GAGAGCTCTACCCTC | 5336 |
| rs527634300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915456 | GACCTCAGGCTGTGG[C/T]CGTGGCATCCACGCT | 5336 |
| rs527637863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906426 | AGGCAATATTTATTT[A/G]TTACTTATTTATTTA | 5336 |
| rs527641367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793172 | TCCCTATTGCTTTCC[A/G]GGGGTGTTGGATAAG | 5336 |
| rs527673985 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81834136 | CCCAGCCAGGTGGCC[G/T]TGAATGGGTGACTTC | 5336 |
| rs527682520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818801 | GAGGAGTGTGGAGGG[C/T]AGCCTCATGAGAACT | 5336 |
| rs527693325 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894642 | CTGTGAGAGGTCGAG[A/G]TGGGCGGATCACTTG | 5336 |
| rs527700230 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865710 | ACCAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs527704458 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797015 | TGTGGTTTGTCATAA[C/T]GGAATTTAAGAGGCG | 5336 |
| rs527722733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867916 | GTGTTAGCCAGGATG[A/G]TCTCGATCCTCTGAC | 5336 |
| rs527737546 | snp | C/T | 4.97393e-05 | 0.0049867 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81891561 | GAACAACCCCCTGTC[C/T]CATTACTGGATCTCC | 5336 |
| rs527745334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823106 | CAGGCGAGGCCTATG[C/T]TGGCTGTGGTTTCAC | 5336 |
| rs527745369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818534 | ACTCATCGGCTGCAC[A/G]GAAATGGAGCTCCGA | 5336 |
| rs527753829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823484 | TGAGCCCCTTCCTGT[C/T]TAGCTTGGATTTGTG | 5336 |
| rs527753836 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809776 | GATTCTAGAGGGAGT[C/G]TCTGATGTCCCAGTT | 5336 |
| rs527777388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845635 | TCTTGTTCCCAGCCT[C/T]GGGTCAGAAAGGTGG | 5336 |
| rs527780407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948080 | GTCGTTGGCAGTTCT[C/T]TACTTTATAAATAAT | 5336 |
| rs527798768 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871452 | CAAGCGATTCTTGTG[C/T]CTTAGCCTCCCCAGT | 5336 |
| rs527807389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822682 | GAATCGCTTGAACCC[A/G]GGAGGTGAAGGTTGT | 5336 |
| rs527809751 | snp | C/T | 0.000132496 | 0.00813822 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919550 | TGTGCTGGGGACCTC[C/T]GCCTATTTTGAGAGT | 5336 |
| rs527810379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876404 | ACCACTGAGTGCGTA[A/C]GACCAGCTTCGGTTG | 5336 |
| rs527812482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924057 | TTTCCAATTCAAATT[C/T]GTATGCTGTTCCATA | 5336 |
| rs527825225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895741 | ACTGGTGTGTGGGCC[A/G]GGGGCTGACCTCGGG | 5336 |
| rs527828241 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896100 | ACCCGAGTGTTGGCA[A/C]CCCCTGCAGGCCGAG | 5336 |
| rs527841064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907471 | AAAGTCCAAAAAGAA[C/G]CTCAAATACCAAAAG | 5336 |
| rs527856014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860479 | GAGGTAGCAATTTGT[A/G]TAATATTTCTACCAG | 5336 |
| rs527858919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780636 | CGACTGGAGTATGGG[C/T]AGTTCCTCTGGAAGT | 5336 |
| rs527862033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931920 | CAATGCTCATTGATG[A/G]TGTCTTTGCGGCCCT | 5336 |
| rs527864336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856502 | CATACTCTCCTGGGT[A/G]TTAGCAAGCTCTACT | 5336 |
| rs527879409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811744 | ATGGTGTATATGTGC[C/T]ACATTTTCTTTATCC | 5336 |
| rs527887252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881217 | CCTCCTTTCCCCGAA[A/T]GTGCCTCATGAGATG | 5336 |
| rs527894106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884979 | TGCAGCCTCGACCTC[A/C]TGGGCTCAACCGATC | 5336 |
| rs527905199 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853352 | AAAAAACAAAACAAC[-/A]AAAAAAAACCATTAG | 5336 |
| rs527920391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838352 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 5336 |
| rs527924264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797577 | CAGCACCTGGCCCAT[A/G]TCTGGCCTGTGGCTG | 5336 |
| rs527942829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864910 | GGTAACTCATTCAGG[A/G]AATAGTTGCCGTCCT | 5336 |
| rs527942916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860130 | GTGTGTTTCACCATG[C/T]CTGGCTTATTTACTA | 5336 |
| rs527970615 | snp | A/G | | | missense | PLCG2 | GRCh38.p7 | 16:81956701 | ATCCTCCAGGAGAGC[A/G]AAGAGGAACTTTACT | 5336 |
| rs527973956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837991 | GCATCCTATATCTGC[C/T]ATCATAGTCAAGAGA | 5336 |
| rs527990155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864555 | TTCTGTGGGCCTCAG[C/T]TTCCTCATGTGTAAA | 5336 |
| rs528007306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815324 | GGGTCTCAGCCTCAG[C/T]AGGTTGGCAGCCACA | 5336 |
| rs528011262 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872208 | TGGTGTGCACCCGTA[A/T]TCCCAGCTACTTGGG | 5336 |
| rs528011458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915996 | AGACATTTAAAAAAT[A/G]TGTACATATTTATAC | 5336 |
| rs528012639 | snp | C/T | 4.99733e-05 | 0.00499842 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940086 | TTTAATTAAGATGTT[C/T]GATTTGGGCTGGCGT | 5336 |
| rs528026581 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864669 | TCATGGTAAACACTT[C/G]ACGAATGTTTCTTAT | 5336 |
| rs528028956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911215 | CATTTCCGAGGAGGC[C/T]GTATTACTTATAGCA | 5336 |
| rs528036287 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794969 | CTTCTCTTATGCTGA[A/G]TAGCTGAGGAATTGC | 5336 |
| rs528054778 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943542 | ATGAGATTTGGGTGG[G/T]GACACAGAGCCAAAC | 5336 |
| rs528066131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865783 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGGGCT | 5336 |
| rs528083897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921927 | AGAAAGAAATGAAAT[C/T]TTGAAAAGTTGTGGG | 5336 |
| rs528089075 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937963 | CCTGGGGGCTGGGCC[A/G]ATGCTGTCTTGAGAG | 5336 |
| rs528095958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794501 | ATTTGCCTTTCAGTT[A/G]CTGGTATGCGGTGAT | 5336 |
| rs528098159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798826 | GAGGGGCTGGCCTCC[C/G]CGGCCTCAGGACTTC | 5336 |
| rs528110006 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893871 | GCTCCATGTTTTCTT[A/T]CGAATTGTAAAAAGG | 5336 |
| rs528140589 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81837171 | AACTCAAAGAACGAG[A/T]ATACATATACATGCA | 5336 |
| rs528146225 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893495 | AGCAGTCACTTCCTG[A/C]GATTGTGGCCTGACT | 5336 |
| rs528155396 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811046 | TAAGGCCACATTTAA[C/G]CTGTGTACCAGAGGG | 5336 |
| rs528159994 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798543 | GTGATGATACCACAT[C/T]ACAGCCTGGGGGCCA | 5336 |
| rs528163916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851216 | CTTGTGGACCTGGCA[A/G]AAATAGTACAGTTTC | 5336 |
| rs528164504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847039 | TCAAGACTCTGTCCC[A/T]TTTCAGGTGCCAGTC | 5336 |
| rs528171284 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820379 | TTGAGTCATCCAGGA[-/T]TTTTCCTTGGTTTTA | 5336 |
| rs528171433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928718 | AGGTGGCTGACACAG[C/G]GTCCTGTCTTGAATG | 5336 |
| rs528182322 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897647 | ACCTCCTGAGTTCGA[C/G]CAATTCCCCTGTCTC | 5336 |
| rs528188044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945609 | GCTCCAACTTGCCCC[C/G]CTCAGCCCCAAATAA | 5336 |
| rs528197831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850949 | CTGCAATCAGTGGGA[A/G]TGGCCCTTTGAACAA | 5336 |
| rs528198259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873085 | TTTTTTCTCATATAT[A/C]ATAATTAGTTATTTG | 5336 |
| rs528200966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954317 | CTGAGGCACTGCGCC[C/T]GGCGACTTGATTCTT | 5336 |
| rs528207824 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790090 | ACTGGAAATAACATT[C/G]GTGTCTACCCCACAG | 5336 |
| rs528216366 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930075 | AGCAAAAGCAGGGTG[A/C]CTTTAGTCTCAGCTA | 5336 |
| rs528220072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876730 | TGGGGTGGGAAGGTC[C/T]TGGGATGTTGCCCAG | 5336 |
| rs528220286 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800546 | CGAAGGACACGATCT[C/T]GTTCCGTTTTATGGC | 5336 |
| rs528235532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879572 | TAGTCCCCATGACGT[C/G]CTGGGCTGCAAGGAG | 5336 |
| rs528238595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956147 | CATATAAATGGCATC[A/G]TGTGATTTGTGATCT | 5336 |
| rs528238837 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913143 | ACTGCAGCTGCTGCC[C/T]AACCACCTCTAGGCC | 5336 |
| rs528246214 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831964 | GTGACTCCTCTTGCC[C/G]TAGCGGAAGGGACTG | 5336 |
| rs528248375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858106 | AGCAGGTCCTAGGGC[C/T]ATGACGGTGTGAAAG | 5336 |
| rs528250953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909462 | TTGCTCTGTTGCCTA[G/T]GCTGTAGTACAATGG | 5336 |
| rs528253932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933832 | TGCCTGCTTTGGGGT[A/G]AAGTGAGAAGCTCAT | 5336 |
| rs528257983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904662 | AGGTGGTGTTGTTGT[G/T]TATTCACCGAGTATC | 5336 |
| rs528262031 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962115 | GGTCTTCGGTCAAGG[C/G]TATACGAGTAGCTGC | 5336 |
| rs528266101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782392 | TCAAGGCTTTTTTTT[C/T]TCTTTTTTTGAAAAA | 5336 |
| rs528267003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809779 | TCTAGAGGGAGTGTC[C/T]GATGTCCCAGTTATT | 5336 |
| rs528294003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886344 | ATGAGCATCCATGCG[A/T]TGTTTGTTGGTCACA | 5336 |
| rs528299071 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961950 | GGCGATCTGGCTGCG[A/G]CATCTGTCACCCCAT | 5336 |
| rs528301317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826390 | GTAGGGGTCCATGGG[C/G]AGGTTCCCTGGGCTC | 5336 |
| rs528309213 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899413 | ATACAGGTGATCCTT[A/C]TTGGTGGATTCTACT | 5336 |
| rs528320721 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786413 | TGAAGCTGAGGTCAG[C/G]CAACATGGAAATGGC | 5336 |
| rs528328625 | snp | A/G | 0.000116035 | 0.00761605 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937879 | CGAGTCCCAGAGGAA[A/G]ATCCTGATGACGCTG | 5336 |
| rs528333369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840346 | CGGTTTTGTGGAAGA[C/T]AACTTTTCCATGGGC | 5336 |
| rs528334705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862008 | GCAGAGCCCTGCTCT[C/T]TGTCAACATGTGGAA | 5336 |
| rs528334804 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866644 | TCTCCCTTGCTCCCA[A/G]GATGAGCTCCACTGG | 5336 |
| rs528402167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917878 | AGGTGCCCGCCACTG[C/T]GCCCAGCTAATTTTT | 5336 |
| rs528415092 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885652 | AATATAGCCATAACA[C/G]TCCTCTTACAGCTTG | 5336 |
| rs528423897 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900509 | TGCCCCCCGAGCAGC[A/G]CCCGGTTTCTGTCGT | 5336 |
| rs528427024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874003 | ACCCTCTGGGGTGCC[C/G]TAGATTGCCCCGTGT | 5336 |
| rs528437969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950633 | AGAAAACTTTAATAC[A/G]TTTTTTAAAAATAAT | 5336 |
| rs528460334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955421 | CCAAGCTTCACAGAG[G/T]AGTCAGGGATCCTCT | 5336 |
| rs528474587 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81873865 | GTTTCCACTGTGGTA[A/G]CATTCCACATGAGAG | 5336 |
| rs528477681 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874771 | CTACGTTCCACCTCT[C/G/T]GAGCTTCAGAGTTTC | 5336 |
| rs528481968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926318 | TGTGGTCAGAGGTGC[A/C]TTTTGGAGAGTCCCT | 5336 |
| rs528487351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922450 | TGCTTTAGCGATACT[A/G]TAGTTAGCACTTAAG | 5336 |
| rs528495882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855205 | CTCAAAAAAAAAAAA[A/G]AAAGAGAAGAAAAAG | 5336 |
| rs528506592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877207 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 5336 |
| rs528513191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851525 | GTTGTTGTTGTTGTT[A/G]TTGTTGAGGCGAAGT | 5336 |
| rs528528362 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862841 | TGTGCCACTGAGCTC[C/T]AGCCTGGGCAACAGA | 5336 |
| rs528534686 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828623 | ATCAGCGAGTCCTTG[C/T]GGGTCAGCAGAGGGT | 5336 |
| rs528536394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806302 | CATTCTCCATGTGGC[A/G]GGTACTATGATCATC | 5336 |
| rs528536851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854884 | GAGCTGAATAAGTGA[C/T]GATTAGATAGTTTTA | 5336 |
| rs528570326 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959145 | TGGTTGGTAGAGTCA[C/T]AACTTCTCAATGAGT | 5336 |
| rs528581928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901974 | CTCATTACACAAAAA[C/T]GGTGAAGGGACTTTG | 5336 |
| rs528596478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810062 | AGTGGCGTGATCTCA[A/G]CTCACTGCAACCTCC | 5336 |
| rs528597544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832387 | TTTTGAGTAGAATCT[C/G]TCCCCACCCTGCCTT | 5336 |
| rs528624799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858417 | ATTCTGCTGCCTTTA[A/G]CCAACATGGGCTACA | 5336 |
| rs528650075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840743 | GGCTCGATTCCTAAC[A/G]GGCCACAGACAGGTG | 5336 |
| rs528663377 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947930 | TTTTTTGTATATGAT[A/G]TTTCCATAGTCAGAT | 5336 |
| rs528664181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817723 | ACTCCCAGACTCAAG[C/T]GACCCCCATGCCCTT | 5336 |
| rs528674140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914134 | AAACCTGCTGTGTGC[C/T]AGGCCCCAGGTGGGG | 5336 |
| rs528685417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867160 | AGAGTCACACTGGAC[C/T]GTCTCCAGGGCAGCG | 5336 |
| rs528687097 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844539 | GGTGGCCAGGCTGGT[C/G]TCAAACTCCCAACTT | 5336 |
| rs528693763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918942 | TGCTAGTTGAGTCAC[C/T]GAAGACAAGATTTAA | 5336 |
| rs528701152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821742 | ATAGATCTTTCTCCG[A/C]TAACTTGCCAAGCAA | 5336 |
| rs528716146 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795824 | CCTGCTTTGGCCTCC[A/C/G]AAAGAGCTGGGATCA | 5336 |
| rs528723555 | in-del | -/AA | 0.49949 | 0.0159663 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907037 | GACAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 5336 |
| rs528736361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894783 | GAGGCCGAGGCACAG[G/T]AATCACTTGAGCCTG | 5336 |
| rs528752702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922832 | CAGGCAGAAAGCATG[A/C]AAGCAAATTCATTGA | 5336 |
| rs528760225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951460 | CTATTAGATAAAACA[A/G]GTTTAGGATCTAGAT | 5336 |
| rs528770736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951008 | CAAATTTTGTTTTGA[A/G]ACAGTGTTTTTTTCT | 5336 |
| rs528780805 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821314 | ATAATGGATTGTTGT[C/G]TCTTGCTGTGTAACA | 5336 |
| rs528784405 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945181 | GGATATTGTTTGAAG[A/G]TGATAAAGCAACTGA | 5336 |
| rs528791416 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898951 | GCACTTTCGGAGGCT[C/G]AGGCGGGTGGATCAA | 5336 |
| rs528805574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874232 | GATCTGGCTATAAAT[A/G]GGGTCACATCTCGCC | 5336 |
| rs528809352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902947 | ATCACAAGAACAGCA[C/T]GTGAAAGGCCCGCCC | 5336 |
| rs528815211 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913536 | AGCCTAAGCTCTTCA[C/T]TCCAGAGTCTCTAGC | 5336 |
| rs528820384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851760 | TCAAGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 5336 |
| rs528836356 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920198 | ATAGGCCATTGTAAG[G/T]CCCTGGCTTTTTCTC | 5336 |
| rs528848781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840371 | ATGGGCCAGATTGGC[C/T]TGGGGGGATAGTGTG | 5336 |
| rs528865899 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804834 | GAAGTGCTGCTGGCA[C/G]CAGGATGAGAGAGTG | 5336 |
| rs528879208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813119 | AGCATGATGCCTGCA[C/G]CTTGTTCTTTCTGCT | 5336 |
| rs528879850 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866665 | GCTCCACTGGGGCAC[C/T]AGCGTGAGAGGACGC | 5336 |
| rs528910114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870242 | ACCAGGTGTTTTGCA[A/G]GTATGTTGTTCACTT | 5336 |
| rs528917013 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866286 | ATGAGAGGATGCTAG[C/T]CTCTCCCTTTCTCCC | 5336 |
| rs528932737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942461 | GCACATCCATATTCA[C/T]GGGAGGAATGAAATA | 5336 |
| rs528933421 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889724 | CAGTGGTGGGATCTC[A/C]CCTCACTGCAACCTC | 5336 |
| rs528955248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816970 | GCTTTTTTTCCTATG[C/G]CCATTGCACAGTTAC | 5336 |
| rs528967750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795005 | TTGTTTTCAAGAGTT[A/G]TCTTCTATCCTGGAT | 5336 |
| rs528968507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898379 | ACATTTTGATACCAA[C/T]TTACTAGGTAGCCTT | 5336 |
| rs528980101 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890196 | TTGCTAATCTTGTAA[C/T]CTCCAGAAAAATGGC | 5336 |
| rs528994010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946395 | AAGCATGAGACATCA[C/T]ACAAGAATTCCTTTT | 5336 |
| rs528994810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869837 | AGCCACTCCATGAGT[G/T]ATGGGATATAGTAGA | 5336 |
| rs529009734 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778556 | TTTCTTAAAGAACAT[A/T]TTAGCTTCTTCCCAT | 5336 |
| rs529013744 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827881 | GGATCACCTGAGGTC[A/G]GGAGTTCAAGTCCAA | 5336 |
| rs529018143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820802 | ATTTTTGTATTTTTA[G/T]TAGAGGCAGGGTCTC | 5336 |
| rs529028096 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904632 | TCCCTCTGTGTGCTA[A/G]AGAAGGCTGGGCACA | 5336 |
| rs529053379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880127 | ATGCCTGTAGTCCTA[A/G]TTACGCAGGAAGCTA | 5336 |
| rs529054083 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959196 | AAGGAGTGTAACTGT[A/G]AAAAACGATGGCTGT | 5336 |
| rs529068283 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832876 | GAGCAGGCTAAGTGC[C/G]CAGATAGGAAGGTGT | 5336 |
| rs529069282 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877386 | GCGTGAACCTGGAGG[C/T]GGAACTTACAGTGAG | 5336 |
| rs529070766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828724 | AGAAGCCAGCCGTCA[C/G]AGCCTCAGCCTTCCG | 5336 |
| rs529083502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879855 | AAGAGCCTCTTCATC[A/G]TGCAACAGTTGGCAC | 5336 |
| rs529092874 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962591 | TGTGTACATAGAGAA[G/T]TAAGTGAATGAGTCA | 5336 |
| rs529099655 | in-del | -/AG | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834549 | GCTGAGATGATGGAC[-/AG]AGAGCACTCGTCACG | 5336 |
| rs529108772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836549 | AGTTTGAGACCAGCC[G/T]GGTTAACATGGTGAA | 5336 |
| rs529128240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909873 | CCTGTCAGACCGCTG[A/G]GGTAGTAATACAGTG | 5336 |
| rs529132656 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959584 | GGGCTGTTATCTGGT[A/G]CTATCACTCCAGTTA | 5336 |
| rs529137107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933933 | TGGCCTGGGCACTGG[C/G]TAGTGGTCCCCTTGG | 5336 |
| rs529147319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862879 | CCCATCTCAAAAACA[A/G]AAACAAAACAAAACA | 5336 |
| rs529153685 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951735 | ATATATTACAACTAA[A/G]CATTTATTCTGGAAT | 5336 |
| rs529154017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810124 | AGCCTCCTGAGTAGG[C/T]GGGACTACAGGCACT | 5336 |
| rs529161693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862336 | ATGGTAGCAGCGGGC[A/C]TTTGTTTACAGCCTT | 5336 |
| rs529192486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883067 | CCTTGAGATTCCGAT[A/G]TCAGGGTCCCTCTGA | 5336 |
| rs529196987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938193 | GAGGTCAGCCTCTGG[C/T]CGGAAAGAGAAAGAA | 5336 |
| rs529205694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870739 | AGCTGTCTCTTCAGC[A/G]TGCCAATAAAATAGC | 5336 |
| rs529219044 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962151 | CCTGCTGGAACCTCC[A/G]AACAAGCTCTCAAGA | 5336 |
| rs529313349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877569 | GCTCCAGGGAAGGAT[A/G]TGTTCCAGACATCTT | 5336 |
| rs529325085 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843921 | CTTTCCTTTCCTTTT[C/T]TGTTTCTGTTTCCTT | 5336 |
| rs529325965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803180 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 5336 |
| rs529340929 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830524 | GTTGGCCATGCTGGT[C/G]TTGGAACTCCTGACC | 5336 |
| rs529342403 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844336 | TCTTTCTTCTTTCGG[A/G/T]TGGAGTTTCACTCTT | 5336 |
| rs529370247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877371 | TGAGGCAGGAGAATG[C/G]CGTGAACCTGGAGGC | 5336 |
| rs529379347 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845628 | ACTAGAATCTTGTTC[C/G]CAGCCTCGGGTCAGA | 5336 |
| rs529387372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955801 | CTGGAGGTTGTACTG[A/G]TGGGGGAAGTAGAAA | 5336 |
| rs529390330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802759 | TATTTTTAGTAGGGA[A/C]GGCATTTCATCATTT | 5336 |
| rs529395288 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898957 | TCGGAGGCTGAGGCG[G/T]GTGGATCAACTGAAT | 5336 |
| rs529414275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829043 | GATGACAAGGACTGC[C/T]CCCTCTGCCCTGTCT | 5336 |
| rs529419030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883790 | AAACTAGCACAGCTT[G/T]CCTTAAACAGGTGAT | 5336 |
| rs529445091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837136 | AAAAGCAAACAAAAA[C/G]AAAAAAAGACAAACT | 5336 |
| rs529450741 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959587 | CTGTTATCTGGTGCT[A/G]TCACTCCAGTTACTC | 5336 |
| rs529461048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867779 | CTCGGCTCACTGCAA[G/T]CTCCGCCTCCCGAAT | 5336 |
| rs529465243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910446 | CACATGTAATGTCCC[C/T]GCCTCTGAGGCCCTG | 5336 |
| rs529465269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914958 | TGGTCTCTACCCACT[G/T]CATGTCTGTCTGGGA | 5336 |
| rs529473884 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788005 | CCACCTTTTGGCTAA[A/T]ATAAATAGTGCTGCT | 5336 |
| rs529485504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863476 | TTGAGTTGCTTCCAC[G/T]TTTTGGCAATTGTGA | 5336 |
| rs529489733 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961793 | TTAAACATGTAGTGT[C/G]TACGGTATGCCAGCA | 5336 |
| rs529500263 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887293 | CCCAGCTAATTTTTT[C/G]TGTTTTTAGTAGAGA | 5336 |
| rs529529342 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892970 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTCC | 5336 |
| rs529537692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792231 | TCACACCTGTAATCC[C/T]AGGACTTTGGGAGGC | 5336 |
| rs529546562 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808831 | CTCCATAGCCTCTGT[A/G]GGCCTGGCCTCTGTT | 5336 |
| rs529552302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947658 | GATAGAGTTTACAGC[C/T]CCAGAAAACTGTCAA | 5336 |
| rs529556272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838409 | TATGAAATGTCTTTA[C/T]TAAAATATAACTTGC | 5336 |
| rs529559000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871080 | ATGATGAAAGCATAC[C/G]ATTTTCATCCATTAG | 5336 |
| rs529592431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848498 | CTGCCTTTGTACATG[A/T]GCGTTTGCATTTCTC | 5336 |
| rs529595864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875906 | CTGTGACGATGTTTG[C/T]GGAGGAGCTCAGAGA | 5336 |
| rs529603209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791804 | TCCTGACCTCTCGTG[A/T]TCTGCCCACCCTGGC | 5336 |
| rs529617665 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918974 | AATTTTGAGGTGGGG[A/G]GGATTGGCAAACATT | 5336 |
| rs529640198 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823554 | TTTAAGAGACAGGAT[C/G]TGGCTCTGTCGCCCA | 5336 |
| rs529645813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844609 | TTACCGGCGTGAGCC[A/G]CTGTGCCTGGCCCAC | 5336 |
| rs529648591 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924947 | GTTGAGGTCTCTTCC[A/G]GGCACACTGGCGTTC | 5336 |
| rs529667889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896700 | CCAAACCTGTTTCTA[C/T]AGGCGGAATCCAAGC | 5336 |
| rs529679819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827485 | TGAGTCACTGTACCC[A/G]GCCTGCATTTATTTC | 5336 |
| rs529698225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924643 | GCAAGATGCCTTAAT[A/C]CAGGGATTATCAAAC | 5336 |
| rs529709598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853376 | CCATTAGACCCTGAA[C/G]TGGTACAGCATCATT | 5336 |
| rs529710466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804964 | ATTTATTTGTAGTGT[C/G]TAGTCATTACAATCT | 5336 |
| rs529712677 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894053 | AGGCAAACAGACACC[A/C]GCTGTGTTTTGGCAG | 5336 |
| rs529731680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878929 | CGTTCCCAGGTGCCT[A/G]TGCCAATGAGCTTCC | 5336 |
| rs529735848 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859620 | GCTCACTGCGAGCTC[C/T]GCCTCCTGGGTTCAT | 5336 |
| rs529748380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893393 | TTGTTAATTCATCTT[C/T]TGCAGCTTTTTTTGC | 5336 |
| rs529771288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808356 | CCTGAGGTCAGAATG[G/T]CCAGGGCACCCTTTT | 5336 |
| rs529776248 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781549 | GTGTTTTGCTTTTTA[A/G]TAGCTGCTCACAGGT | 5336 |
| rs529791476 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856883 | GGAAGGTCATTCCCA[C/G]AGAAAGAGATGTGAG | 5336 |
| rs529803147 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955277 | CAGAGTATGGTCTGA[A/G]TCCGTGTTTTTCTAA | 5336 |
| rs529804833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780954 | ATCACTTGAACCCAG[A/G]AGGTGGAGGTTGCAG | 5336 |
| rs529806249 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846944 | ATTGGACACCAGTTT[A/G/T]GTGTCCTCTAGTTCA | 5336 |
| rs529808033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839183 | ACTCTTAACATACAT[C/G]AGTTCAGGTGAAAAC | 5336 |
| rs529816015 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926464 | CATTCATAGATGGAT[A/T]ATGTCCCGTGTTGTT | 5336 |
| rs529825759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830704 | TATTTTATATATGTA[C/T]ATATATGAATGAAAT | 5336 |
| rs529833031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816028 | GATTGTGCCACTGCA[C/T]TTCAGCCTGGGTGAC | 5336 |
| rs529839450 | in-del | -/GGGACTCAA | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853998 | GCATTTGTAGCTTTT[-/GGGACTCAA]GGGAAAAGGTCATCA | 5336 |
| rs529841447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957115 | ACCAGCGTGCCCAAC[A/G]TGGAGAAACCCTGTC | 5336 |
| rs529845115 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961059 | CAACAGGGCACAAAT[A/C]TTTTTGCAAATGGAT | 5336 |
| rs529848223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865392 | GTGAGGGAGGGGCTC[A/G]CCTAGGGAGAAAGCG | 5336 |
| rs529852475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842715 | GGAGCCTGAGAGAGA[C/T]AGAGAATCAGTAGCG | 5336 |
| rs529864691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843111 | TTCAAGCAGGAAACT[C/T]GGCCACTGAGCCCCA | 5336 |
| rs529869406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916934 | TGAGCCACCACGCCC[A/G]GCCAGGACTTTGTTA | 5336 |
| rs529869704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912346 | GCTGGGATTTCAGGT[A/G]TGAACCACTGTGCTC | 5336 |
| rs529884237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868941 | GTCCCTGGACATACC[C/T]GAAGGGTGGAGACCA | 5336 |
| rs529895154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819762 | GCTAATTTTTGTATT[G/T]TTAGCAGAGATGGGG | 5336 |
| rs529898581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893069 | TTTCACTATGTTGGC[C/T]AGGCTGGTCTTGAAC | 5336 |
| rs529901313 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929568 | GCCTGGCTAATTTTT[-/G]TATTTTTAGTAGAGC | 5336 |
| rs529907711 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935097 | AACTTGGTGGCTGAA[A/C]ACAACATTTATTCTT | 5336 |
| rs529913502 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835493 | CTGAGGTATGAGAAT[C/T]GCTTAAACCTGGGAG | 5336 |
| rs529930951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916619 | CTTAAAGTCTACCCT[C/T]AGCAATTTTCAAGAA | 5336 |
| rs529936458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940984 | CTGGATTCCTCAAGA[G/T]GTCACTGTTCCCTTG | 5336 |
| rs529946515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949140 | ATGGAAAGAAAGGAA[A/T]AGGTGGGCTGGGAGG | 5336 |
| rs529957300 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897048 | TGCAACTATTCAGCC[C/G]TGTTGCTGAAGTGCA | 5336 |
| rs529972806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920977 | CTGGCACGCAGCAGG[A/C]CAGGACAGGGCCTCT | 5336 |
| rs529978466 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927378 | TGTGACAAGCCGGCC[A/G]TGTTTTAATCAGGTT | 5336 |
| rs529984601 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797989 | GTACCCTCCACCTCA[A/C]CTGGCTAATTTTTGT | 5336 |
| rs530006118 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961925 | GTTAAGATTGCTGAT[C/T]GGATGTGAGGGCGAT | 5336 |
| rs530006231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831556 | GAACCTCATCCAACC[C/G]CATACTCCAGTTGGG | 5336 |
| rs530007671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904398 | GTTACATGACCCTCA[A/G]CTTACAGACGCTTGC | 5336 |
| rs530008976 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81954432 | TGTTACATAGGTATA[C/T]GTGTGCCATGGTGGT | 5336 |
| rs530009837 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841772 | TCATTACATGTTCTT[C/G]TGCTGTGTATCTCAC | 5336 |
| rs530010488 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846739 | ACAATCCCAACCAAA[A/T]TCTAATAGAGATACA | 5336 |
| rs530041512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882457 | AGGGAACTCTGGATC[A/G]TGGCTTCTGAGGAGG | 5336 |
| rs530042945 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961654 | AATTGCCTTGTTCCA[A/G]GTAAGACTGATCATA | 5336 |
| rs530047864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846382 | TATTCTGCTCGCCAT[A/C]CCACTCCTGCACTCT | 5336 |
| rs530069184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835466 | CCGGGTGTGGTGACA[C/T]TACTTGGGAGGCTGA | 5336 |
| rs530078262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781976 | TCCCGGGTTCACGCC[A/T]TTCTCCTGCCTCAGC | 5336 |
| rs530089188 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778074 | AAAAACCAAAAACAC[A/C]CACACACAAAAAAAA | 5336 |
| rs530105739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808848 | GCCTGGCCTCTGTTT[C/T]CCCCTATGCAAAATG | 5336 |
| rs530134028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785739 | CTTGAGGTCAGGGGC[C/T]CTTCTCACACTTCAG | 5336 |
| rs530142575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785920 | TACTAAAATCAGTTC[A/G]CTCTTTAATTCTGCC | 5336 |
| rs530144244 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947271 | TGTAGGGAGCCAGGG[C/G]CGTTGTGTGGGGTTC | 5336 |
| rs530152905 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811329 | TCAGTTATGAGCACT[G/T]TGGTTGGCAGTATCA | 5336 |
| rs530156886 | snp | A/G/T | 0.000300607 | 0.0122565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937740 | TGACTTACAGCAGGC[A/G/T]TTCACTTTCCTTCCC | 5336 |
| rs530159953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885365 | AACAGGATTTCCCCA[C/T]GTTGCTCAGGCTGAT | 5336 |
| rs530160338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941518 | TGAATTCCTTAGCAA[A/G]TTACTAGATGAAACA | 5336 |
| rs530162200 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883884 | GGGGGGTTGTGTTGC[A/G]CCTTGGTTTTCCACT | 5336 |
| rs530165886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932732 | GCAGAGGGGACTGGT[C/T]CATGGGTGCCCTCGC | 5336 |
| rs530168573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812249 | AGAGACGAAGTTTCA[C/T]CGTGTTAGCCAGGAT | 5336 |
| rs530204338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950153 | ACTTACATTTAATTT[A/G]GTGAATAGGCTGAAT | 5336 |
| rs530246512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798561 | AGCCTGGGGGCCACT[C/T]CACTGTCACAGGGCT | 5336 |
| rs530248360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915038 | CACTTTTTCAAACCC[C/T]CTCTGGTCAGGGTAT | 5336 |
| rs530284214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954806 | AGTAAACTTACATGT[A/G]CGTGGGTCTTTATAG | 5336 |
| rs530298767 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929939 | TGGCTCATTGGTTCT[A/G]AGTAGAAATCTTGGA | 5336 |
| rs530303736 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81908712 | TGAATCCCAGGCTTC[A/G]TTTGTCTAGCTCTTC | 5336 |
| rs530310738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954407 | GATACAAGTGCAGGA[C/T]GTGTAGGTTTGTTAC | 5336 |
| rs530326989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943653 | AAGTCAGAATCTGCA[G/T]TTTAACAAGATTCAC | 5336 |
| rs530338123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859744 | GGTTTCACCATGTTC[A/G]GCAGGATGGTCTTGA | 5336 |
| rs530338177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851238 | TACAGTTTCTGTGAA[A/C]CATTCATTTAGCTGC | 5336 |
| rs530354831 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782886 | TGTTTTCAAAGGAAC[G/T]GTGTCAGCCACTGCA | 5336 |
| rs530360179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876770 | AGGCCCAGTGCCACC[C/G]CTGTCCCTTGGTTAG | 5336 |
| rs530371937 | in-del | -/ATATA | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952128 | AAAGGTACAGAACTT[-/ATATA]AGAAAAAAACATAAA | 5336 |
| rs530382993 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794117 | ACCAAGAGAAAGGAG[A/T]CTCAGTGCTCATCCT | 5336 |
| rs530393089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949664 | AAGAGAGGGAAACCA[C/G]TGAATAATTAATTTT | 5336 |
| rs530397713 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930352 | ACGCCACATTTCTCT[C/G]CTAGTTTCTGGTGAC | 5336 |
| rs530398058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876429 | CGGTTGTGAAAGGGC[A/G]TGTGCCTTCAGCCAC | 5336 |
| rs530400601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879532 | TGCTTCTCAGAGGCC[C/T]GCGATTCCCTTTCTA | 5336 |
| rs530402970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819855 | TCCCAAAGTGCTGGG[A/T]TTACAGCTGTGAGCC | 5336 |
| rs530410743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798519 | GGTGAAGTTCTGGAA[A/G]TAGAAACAGTGATGA | 5336 |
| rs530412276 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785888 | AGTTCATGCCCTGTT[A/G/T]ACTAAACCCCTTTCA | 5336 |
| rs530414178 | snp | C/T | 0.000579123 | 0.0170066 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921438 | TGATAATATCAAGCC[C/T]AGTTTCAGGGAAAAT | 5336 |
| rs530460299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805511 | CTCAGAAAAAAAAAA[A/C]AAAAAAACAAAACGC | 5336 |
| rs530478299 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821882 | GATGTTTTTTTTTTT[-/TTC]TTCCAGAGCAGCACA | 5336 |
| rs530497122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928837 | TGTAAGTGCTAAAAC[A/T]AGGTCTCGTACATAA | 5336 |
| rs530499064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801713 | TGAGGTGGTGTCTTG[C/G]TTTGTCACCCAGGCT | 5336 |
| rs530499252 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931366 | TGGAAAGTAGACGTC[A/C/T]CCATCAGTGCTAACC | 5336 |
| rs530546906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850910 | ATTTAAGATGGGGCC[C/T]GCTTATTTTTGTTTC | 5336 |
| rs530554387 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838942 | TGACACCACTCTGAC[C/T]CCATCAGTGAGTCTT | 5336 |
| rs530556181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801513 | AGTACAGCACGATAG[A/G]TTGATCTGTCCTGTC | 5336 |
| rs530573680 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900559 | CCCTCTGTGGGGCAG[A/G]TGCAGAGGTGTGTGC | 5336 |
| rs530573937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835552 | CCATTGCTCTCTAGC[A/C]TGGGCGACAGAGCAA | 5336 |
| rs530580736 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935650 | TGTTGACTGCCGGGC[C/T]ATCCCACCACAGCTG | 5336 |
| rs530594527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882520 | ACCAGCTCTCCCTCT[A/G]CGGGCGGGTGGTGTG | 5336 |
| rs530600387 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942051 | TGTAGCTTTTGGTAC[-/A]ACCTTTACGTTCCTA | 5336 |
| rs530601779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953862 | GGTGATAAAGGGTTG[C/T]AGTTATAGAAGCATT | 5336 |
| rs530604563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949215 | AGTTAAACAGACGGT[A/G]GAGAGCTATTAATGA | 5336 |
| rs530612379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897196 | GACTCCTGGTTTGGG[A/T]TCCTTGTTATTTCTG | 5336 |
| rs530613784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861582 | GCTGGGCCACCCTCT[C/T]GTGTTACTGAGGTGG | 5336 |
| rs530629506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885712 | CCGATACCCAGCCTG[C/T]ATTTGGATTTCATTG | 5336 |
| rs530633849 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857406 | AATCCTGTATCTTCC[A/G]CTGTCTCAGTGTGCT | 5336 |
| rs530644331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942084 | CTTGACGCTGTAACA[G/T]ATTTCTTTTTATGGT | 5336 |
| rs530650008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865754 | GCTCCACTGGGGCAG[C/T]AGCGTGAGAGGACGC | 5336 |
| rs530664008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953395 | GGGTATGTGAGAACA[C/T]TGTACTATTACTGTA | 5336 |
| rs530664309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957870 | TGAATGACTGGCAAA[C/T]GTACAGAAAGAGAAA | 5336 |
| rs530670205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918970 | TAATAATTTTGAGGT[C/G]GGGGGGATTGGCAAA | 5336 |
| rs530675699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913042 | ACTTGCTGAAGCATG[C/T]AGCCACTAAGTGGTG | 5336 |
| rs530677703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839983 | GGTCCCTTGAGCCTA[C/T]GAGTTCAAGGATGCA | 5336 |
| rs530712899 | snp | C/G/T | 5.20007e-05 | 0.00509879 | missense | PLCG2 | GRCh38.p7 | 16:81889202 | GATCTGAACAAAGTC[C/G/T]GTGAGCGGATGACAA | 5336 |
| rs530718519 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777318 | CCCTATCCATGTAGA[C/T]TTTGTAATAATAAAT | 5336 |
| rs530727151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866107 | CACCAGCATGAGAGG[A/G]TGCTGGTCTCTCCCT | 5336 |
| rs530727804 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816063 | CATGACTTCATCTTT[A/T]AAAAAAAAAAAAAAT | 5336 |
| rs530733095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869357 | GACTTAGCCTCTCTC[A/T]TGAAGCCGTGGCTTG | 5336 |
| rs530733294 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802458 | CTTCCAGCTTTTGCT[A/G]CCAAGTGTTCCCAGT | 5336 |
| rs530742378 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886637 | TGGGATAGGAAGGGG[C/G]TTAAAAGTATGTTTC | 5336 |
| rs530746590 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843997 | TCTTTTTTTTTTTGA[A/G]AAGGCGTCTTGCTCT | 5336 |
| rs530748584 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917410 | CCTTCAGATATATAC[C/G/T]GAGAAGTGGGATTGC | 5336 |
| rs530768201 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876848 | AACTGCTGCCTCCAC[G/T]GTGCACCCGTAGCAT | 5336 |
| rs530772597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879777 | TGTGTACAATGCACA[G/T]AAAATGGGCTGGTGC | 5336 |
| rs530818861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789905 | GGCGCCGCCCTAGGC[A/G]CTAGAGATACAGCAG | 5336 |
| rs530827246 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958603 | AAGACAATTTCTAAT[C/T]AATGGTGACAGCTTG | 5336 |
| rs530856798 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875063 | CTTCCTTCCGGGTTC[A/T]AGCGATTCTCCTGCC | 5336 |
| rs530857716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820328 | CCCACCCTCCCCAGC[A/C]TGCACACTCCCTGCC | 5336 |
| rs530861170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842788 | CCGGCCAGCAAAGGG[G/T]TCGGTGGTGTAAAGC | 5336 |
| rs530862123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933328 | GAGCAAAGGAAGAAG[A/G]CCCCATCCCACTCTT | 5336 |
| rs530874030 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805546 | AAACAACAAAAAAAA[A/C]CAAAAACAAAAGCTC | 5336 |
| rs530888436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904606 | GTTCCCTCTGGACTG[C/T]GGCCTGCCTTTCCCT | 5336 |
| rs530896109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904959 | GTGGTGCAGTCTCAG[C/T]TCACTGCAACCTCCA | 5336 |
| rs530910118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929442 | GCTGTGTCACCCAGG[C/G]TGGAGTGCAGTGGCG | 5336 |
| rs530911032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854418 | GAACTCCAGCTTCTA[A/G]TTGGCTCATGTTAAT | 5336 |
| rs530921641 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875694 | CTACCCTGCTACCTC[A/C]TGATCAAACCTGTGA | 5336 |
| rs530934928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809363 | CAGCTCCCTCACCCT[C/G]AGTCAGGACACTCCT | 5336 |
| rs530945260 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962089 | ACGACCAACCCCGAT[A/G]GAGGAGGACCGGTCT | 5336 |
| rs530956914 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961947 | GAGGGCGATCTGGCT[A/G]CGACATCTGTCACCC | 5336 |
| rs530966505 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782233 | TGAATGAGCTTATGA[C/G]ATACAAGAAAAACCT | 5336 |
| rs530976087 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946458 | TCCCAGCATCCTCCT[G/T]TCCTGGAGAATGCTG | 5336 |
| rs530997591 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858034 | CAGGAAATAACCCAC[G/T]TGTCATCCCTGTGGT | 5336 |
| rs531006925 | in-del | -/AAAA | 0.41811 | 0.185038 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858439 | TGGGCTACAGGGGGG[-/AAAA]AAAAAAAAAGGGACA | 5336 |
| rs531010038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917962 | TCCTGACCTCAAGTG[A/T]TCTGCCTGCCTTGGC | 5336 |
| rs531025460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835949 | AGTCTTGGGTTAGGA[A/C]CCACCCTAATCCAGC | 5336 |
| rs531032471 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800060 | CTTTTCATTGCACTC[A/G]TCTGTAAAATAGGAT | 5336 |
| rs531038469 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933773 | CTCAAGGTCCCCCCT[A/T]GGCCAATAAAAGTCT | 5336 |
| rs531049506 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825025 | AGAAATGCAGGTGGC[C/G]TCTAGAGCTGGGAAA | 5336 |
| rs531073664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847397 | GCCATTGGTGACCAA[C/G]TCAGTCTTTAGCCCC | 5336 |
| rs531076282 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868606 | TACATGAAGAGTGTC[-/AT]ATAGTTACTCCTGAT | 5336 |
| rs531077840 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81908304 | GACCAGCTGAGGCTG[G/T]CCTCTCTATGTTATC | 5336 |
| rs531096223 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920514 | TTAGGCTGTGGGAGT[A/G]GAGATCAGAGAAGGC | 5336 |
| rs531122996 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870327 | ACTGAGGGTTTGAAA[G/T]GGTCAAGGAAATTGC | 5336 |
| rs531159781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847587 | TGTGCCAGAAAATGG[A/G]GTTGGAGACCAAATA | 5336 |
| rs531162575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956364 | ACACTTTTGCAGTCA[C/G]GTAAAGGCCAGAAGG | 5336 |
| rs531173125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906969 | CTTGAACCCGGGAGG[C/T]GGAGGTTTCAGTGAG | 5336 |
| rs531173915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881125 | CGTGGATAGAGATGA[A/G]CAGTAGCAACAGGAA | 5336 |
| rs531196455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851499 | TTTTACTCTTTTCAC[A/G]TGGCCTTTTTGTTGT | 5336 |
| rs531203999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926292 | GGAGGCCCTGGGGAG[A/C]CATCATGTGGTGTGG | 5336 |
| rs531211286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880785 | CTAACATCAACTAAA[A/G]TGATATTTTTAATGA | 5336 |
| rs531228315 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847356 | ATGAGAGCCTAATTA[C/T]AAAGGCATGATTGAT | 5336 |
| rs531240623 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833792 | GGCTCGAGCTGTCCT[C/G]CTGCCTTGGCCTCCC | 5336 |
| rs531244751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784231 | CCTCCCCATTCCCCT[C/G]ATTTGCATCCTAGTC | 5336 |
| rs531258374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877182 | CAGAAGTGTCGGGCA[C/T]GGTGGCTCACGCCTG | 5336 |
| rs531264276 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807195 | GATTTCACAGGGTCA[C/G]CTCCCCATGTCTTGT | 5336 |
| rs531279259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811049 | GGCCACATTTAACCT[G/T]TGTACCAGAGGGACA | 5336 |
| rs531296358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884043 | ACAGGGCAGCCCCCC[C/T]TACCCCCCAGCGAAG | 5336 |
| rs531303114 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878013 | TTGAGAGGGAGTCTC[A/C/G]CTCTGTCACCCAGGC | 5336 |
| rs531333601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887697 | AAGCACACACACATC[A/T]GGTCGCATATTTGCT | 5336 |
| rs531338096 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878657 | AGAGCACTTCATCTT[A/G]GCACGTCAGCCATCA | 5336 |
| rs531349685 | in-del | -/AAAAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789133 | AAAGTAAAATAAAAT[-/AAAAT]AAATATATACAAAAA | 5336 |
| rs531361281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797038 | AAGAGGCGTTGCTTT[A/C]TTCCACGTGTCATGT | 5336 |
| rs531368044 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81783126 | CTTGTCCTGGTTTCT[A/G]TCTAATTGAAGGTGT | 5336 |
| rs531386706 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931113 | TAATGTTTGTTTTTT[C/T]TTCCTGCATCTTAAG | 5336 |
| rs531391376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823186 | CTTCCCTTCTGATCT[C/G]GATGGATTGTTTTCA | 5336 |
| rs531397191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935502 | GTATTTTTTTCTTTG[C/G]GTGTTTTGAGCTGCT | 5336 |
| rs531401234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807317 | TGAGGGATTGGGGCA[A/G]TGTGCATCTCTGCGA | 5336 |
| rs531411435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906604 | AATTTTTGTAGCCTT[A/G]GTAGAGATAGTGTTT | 5336 |
| rs531424848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896156 | AGCCCCGAGGAGGCT[A/C]TGGCTGGGGAACCCT | 5336 |
| rs531429674 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833197 | ACGTTTGGGGTTCAG[C/G]AACCCCAGAATGAAA | 5336 |
| rs531436762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783816 | TAAGGTAAGATGCAC[A/G]TTAACTCTCAGCAGG | 5336 |
| rs531441667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859425 | CCTCATCACAAATAT[A/T]TGAGCACCTTTAAAG | 5336 |
| rs531448474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826817 | TACCGTGATTTTCTA[A/G]TATGACTCTCAAGGC | 5336 |
| rs531449967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875210 | CTCAGGTGATCCTCC[C/T]GCCTTGGCCTCCCAA | 5336 |
| rs531469681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810835 | ATCGACCTTATTGTT[G/T]AGTGGGAGAGGCAAG | 5336 |
| rs531472087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910865 | AAATTGCCGAGGTGG[C/T]CAGTTTCCAAATTCC | 5336 |
| rs531473955 | in-del | -/TTCT/TTCTTTCTC/TTCTTTCTT | 0.00716784 | 0.0595003 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844931 | AATTGAGACACCATG[-/TTCT/TTCTTTCTC/TTCTTTCTT]TTCTTTCTTTTTTTC | 5336 |
| rs531484989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878305 | TCCCTCTTTTAAGAA[A/G]CCAGGCACTGGATTC | 5336 |
| rs531488598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871789 | ATCGGGGCCTGAGAA[C/T]ATATTATCGGATTGT | 5336 |
| rs531491515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899949 | CCTTAGGAGCAATGG[C/G]TCAGGTATTTGCCAA | 5336 |
| rs531505627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899670 | TCTTGCTGTTCAAAT[G/T]GCCCGAAGCACAGTG | 5336 |
| rs531509564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903232 | TGGTGGTGTCAACAC[A/G]TGGCATGTACCCTAT | 5336 |
| rs531522894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919999 | AGGAAGATCTCACTG[A/G]AAAGGAATGAGCCAT | 5336 |
| rs531534195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924148 | GGTACCTGGGTATGC[G/T]AGGGTTTAGTTACCA | 5336 |
| rs531542974 | snp | A/G | 1.66103e-05 | 0.00288182 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956856 | GAACCAGCTCCAGCT[A/G]TACCAGGAGAAATGC | 5336 |
| rs531550365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911634 | AATTAATTTTGAGAC[C/T]GGGTCTCGCTCTGTC | 5336 |
| rs531550989 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850157 | AAGTCTACTGTAAAA[A/T]GATTTGGAGAAAACT | 5336 |
| rs531556222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800902 | GGGAGGCAGGAGGGT[C/T]AGAGTCAGAGTGAGA | 5336 |
| rs531563425 | in-del | -/TCTC | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803482 | GGACATTTAGGTAGT[-/TCTC]TCTTTTTGGTTACTG | 5336 |
| rs531564059 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789421 | CAGTCTCCCAAGTAG[C/T]TGAGACTACAGGTGA | 5336 |
| rs531582351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822753 | GAGACAAGAGCGAGA[A/C]TCCATCTCAAAAAAA | 5336 |
| rs531596686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779699 | CCAGCTTTGAATGGG[A/G]ACCGGGAGGAAGGTC | 5336 |
| rs531604041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842355 | GATATTCACATATCA[G/T]ATGCCGGCCTGGACA | 5336 |
| rs531609826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927669 | TAGCACTCCACCAAG[A/G]ATGATATCTTTGTAA | 5336 |
| rs531613043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952595 | CGCTCCCAATGGCCA[A/C]AGCTGGAACCATTTG | 5336 |
| rs531613262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874924 | TTTTCTCAGGTGGAC[C/T]ATTTGCTAGGCACTA | 5336 |
| rs531616395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888181 | ATAGGAGGAAGAAAG[A/G]TGCTTGTTTGCACAA | 5336 |
| rs531621749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916131 | CAGTGTTTCTTTTCT[G/T]TCCTCTGTTTTTTTA | 5336 |
| rs531632569 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953060 | TTGCCAAAACTGCAT[C/T]GCCTCAAACAAATTA | 5336 |
| rs531633465 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780167 | GCGGGGTGGTAAAGG[A/G]GTGACATGGCGCGAG | 5336 |
| rs531643444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826455 | AGGTCAAAGTGCTCG[A/G]CCTCGTGTGCCTCAG | 5336 |
| rs531679922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804152 | CAAAGCAGTTGCACC[A/G]TTTACTTTCCCACCA | 5336 |
| rs531693801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794133 | CTCAGTGCTCATCCT[A/G]GAGGCGCCGGATTTG | 5336 |
| rs531711194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885016 | CCTCAGCCTCCCGAA[C/T]AGCTGGGACTACAGG | 5336 |
| rs531722193 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807878 | ACATACTTTTCAACA[G/T]CCAGATCTCTCAAGA | 5336 |
| rs531724700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846066 | TTGTGCCCCACTCAG[C/G]TCCCATTACCAGGCT | 5336 |
| rs531727029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845794 | AACAAAAATGCCCAC[C/T]GACCCCCTCAGACTT | 5336 |
| rs531731078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811456 | TGGGAACTGGTTTCA[C/G]GATGATGTTTCCGTT | 5336 |
| rs531736092 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818937 | CTTTGAATCACAAAA[A/T]TAAATACAGCTTTTT | 5336 |
| rs531745904 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811295 | AGAGATCGGGTATGT[A/T]AAACCTTTAGGTTAG | 5336 |
| rs531757912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914510 | CCTGACTTACATACA[C/T]GCCCCATTCAGTTTG | 5336 |
| rs531758839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793534 | GTGTAGGCTTTTTAT[C/T]CTGACATTTTCACTT | 5336 |
| rs531762957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864595 | AATAGTTCCCGCCTC[C/T]CAGGGCAGATGTGAG | 5336 |
| rs531772596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868511 | CCTGTGGTTTTGGTT[C/T]CTCTGGGTGGCAGGT | 5336 |
| rs531792349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805013 | GTTTACTCCTAAGTA[C/T]AGTGAGCTTCAGTGA | 5336 |
| rs531831629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888333 | CTCTTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 5336 |
| rs531842728 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879181 | GAGGGGGGCCACACA[C/T]TGGGCTCCCTCCAGA | 5336 |
| rs531847769 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944035 | TCCACGGAATTCAGT[A/C]AGATGATGAGCATCC | 5336 |
| rs531849365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781054 | AAACAAACAAACACA[C/G]ACAAACACTTCTTAA | 5336 |
| rs531859829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872066 | AGGTGCAGTGGTTGA[C/T]GCCTGTAACCCCAGC | 5336 |
| rs531891425 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894343 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 5336 |
| rs531908855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831144 | GTCACACACCATGCT[C/T]TGCTCTTCTTTGGTT | 5336 |
| rs531909849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781574 | ACAGGTTGCCCTAAA[A/G]GAGCAGGGGTGGAAT | 5336 |
| rs531936964 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797124 | AGTGTAGTGGGTAAA[C/T]GAGGGAGGCAGCATT | 5336 |
| rs531940923 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782778 | TTAAAATGGGGCACA[A/G]GCAAATACTTGAGTG | 5336 |
| rs531942783 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878638 | GTTTCCATCCCTGCC[G/T]CCTAGAGCACTTCAT | 5336 |
| rs531955200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952833 | AAAATGAAAGTTGGA[C/G]GAGAAATATATTTCC | 5336 |
| rs531962279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834996 | GCAGGGGAAAGGCCC[A/C]TTGCCCACCTCCTGG | 5336 |
| rs531962864 | in-del | -/TTTCT | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889413 | GGTTAGCTGGGATTG[-/TTTCT]TTTCTTTTCTTTTCT | 5336 |
| rs531978618 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878770 | TCTCCTTGATGTTGT[A/T]ACTTGCCTTTGGGAT | 5336 |
| rs531980558 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809396 | CTTGTTCTGCACTGA[C/T]TCCCAGGCTTCCCCA | 5336 |
| rs531988013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957071 | TGGGAGGCTGAGGAG[A/G]TTGGATCACCTGAGG | 5336 |
| rs531992344 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858115 | TAGGGCCATGACGGT[G/T]TGAAAGGGGATGCTT | 5336 |
| rs532001679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860931 | GCAGTGAGCCGAGAT[A/C]GCGCCACTCTACTGT | 5336 |
| rs532023799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804513 | GGATGTGCTTCTTGG[C/G]TTGAGTCAAGAATCA | 5336 |
| rs532025715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881706 | CTGGAGTGCACTGGC[A/G]CAATCTTGGCTCACT | 5336 |
| rs532027565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885302 | GTGCTGGGATTACAG[A/G]TGTGAGCCACCACGC | 5336 |
| rs532028688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878314 | TAAGAAGCCAGGCAC[G/T]GGATTCGGGTCCACC | 5336 |
| rs532036226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830156 | GAAACCCTGTCTCTA[C/G]AAAAAGTACAAAAAT | 5336 |
| rs532047393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936565 | GAGGGATGAGAGGAC[C/T]GAAGGCTGCTTGGCT | 5336 |
| rs532052240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931860 | GCCCTGGGAAGGTGG[A/G]TCTGGTTGTCTGGTT | 5336 |
| rs532052503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807889 | AACAGCCAGATCTCT[C/G]AAGAACTCACTGAAT | 5336 |
| rs532059365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940821 | TTCTATATAGTTTCT[C/G]TAGTTTACTTTCCCA | 5336 |
| rs532064820 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881180 | CCAGAAAGTTCTGTA[C/G]AAAAGCCTGTGTGCC | 5336 |
| rs532076158 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869747 | TTTCTTCTGTTTCTC[C/T]AACCATCCATCCTTC | 5336 |
| rs532078952 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960803 | AGATTAAGCTAGCCT[G/T]ACCCCTGGGAGTATA | 5336 |
| rs532096072 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830670 | TGTGTGTGTGTGTAT[A/G]TATATATATACACAC | 5336 |
| rs532102760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900055 | CTATAAATACACAGA[C/T]ACCTTATAGAAATAT | 5336 |
| rs532167255 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956403 | AGACCAAAGGAAAAC[C/T]GGGTTAGATTAAGAA | 5336 |
| rs532175160 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927703 | GGATTTTAAGATCCC[G/T]TTAGACCCCCAGGTG | 5336 |
| rs532186162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780519 | AGTTTCTCTTGCAAA[G/T]GTGTGTGTGCAGTCA | 5336 |
| rs532186914 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81831449 | ACTTGGCCATGAACT[G/T]GGTCTCCTTAAATCC | 5336 |
| rs532188365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819399 | GGAGCTCCTGCGAAT[C/T]CCCTTGTGCAGCCAG | 5336 |
| rs532196503 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935195 | GTGCTCCCTCCGGAG[G/T]GGAAAGCCATTCCCT | 5336 |
| rs532200313 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849422 | TTCTTTAGTTATGTA[C/T]AATTTTTCTGTAAGG | 5336 |
| rs532206223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804207 | CCCATGTCCTCGCCA[A/C]CACATGTTAGTATCT | 5336 |
| rs532221098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956907 | CTCCACCTGCAAAAA[C/G]TTTTGGGGGGTCTCT | 5336 |
| rs532225138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829675 | GGACACCACATTGCA[C/T]CTAGTTTTTGTTTAT | 5336 |
| rs532259982 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862302 | ACGCTGTTTCATTTT[C/T]TGACTTTTCTAGAGG | 5336 |
| rs532278245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823211 | TTTTCAGTTCAGCCT[A/G]GGGGAGGTCTGGCTT | 5336 |
| rs532285930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953053 | GACATTCTTGCCAAA[A/G]CTGCATCGCCTCAAA | 5336 |
| rs532290593 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796111 | ATGAACAGTCTCATC[A/G]CTGGGCTGCATGGAA | 5336 |
| rs532304578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793613 | TGCCCATGAGTGACG[A/G]ATTCTCAAACATATG | 5336 |
| rs532321238 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911523 | TCTCGCAGCAGCCTC[C/G]AGCTCCTGGGCTCAA | 5336 |
| rs532327189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875524 | AAGTAGAGAGAATAG[C/T]GTAACAGACCCCCAT | 5336 |
| rs532329988 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908129 | CCCCAGGGCCTCATG[G/T]CTCTCAGACTTCCCA | 5336 |
| rs532344563 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920853 | CTGTCGTTGAACCTG[G/T]AACGTGGAGTCAGGA | 5336 |
| rs532348367 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930377 | GGTGACTCTTTGGTG[-/T]TTTTGGCTCATGGCT | 5336 |
| rs532355112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920429 | TATACACAATTAAGA[A/T]GTTTTCAGGTAGCAT | 5336 |
| rs532369860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797605 | CTGGTGCTCCTCAGA[A/T]ACCTGGTTAACAGAT | 5336 |
| rs532379638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818997 | TCATCTTATTTCATC[C/T]TTCTAGGCCCACCAT | 5336 |
| rs532384567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839111 | TTTTATTATTTTGCA[C/G]TTCCTATTGTATATG | 5336 |
| rs532393171 | snp | A/G | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778747 | GCAGCCTCAACGAGG[A/G]CTTCAAATTAGGGCC | 5336 |
| rs532403190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785229 | AACAGCAATCAAGGA[C/T]ACCTCCTAGGTGCTG | 5336 |
| rs532407240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834714 | GAGCAGGGTGGGGAG[G/T]AGAACCCACTGGACC | 5336 |
| rs532410892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885323 | GCCACCACGCCCAGC[C/T]CCGACTAATTTTGTA | 5336 |
| rs532423414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801415 | GTATCCCTCAAGCAA[C/T]TTGCATGTTTTTGCT | 5336 |
| rs532425507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846086 | ATTACCAGGCTTGTG[C/T]TCCATTTCCCAGCTG | 5336 |
| rs532438319 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849943 | CTTTGGAAAACAAAC[C/G]TTAATACCTTTCAAG | 5336 |
| rs532449104 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812621 | GCAAAATTTTTCTTC[C/T]ATTCTGTATGTTGCC | 5336 |
| rs532469648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838636 | AAGGGGAGGGAGAGC[G/T]TTAGGACAAATACCT | 5336 |
| rs532476250 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853354 | AAAACAAAACAACAA[A/C]AAAAAACCATTAGAC | 5336 |
| rs532481467 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81897965 | CCTTTCAATGAAGGC[A/G]TATGATTTCTCCATC | 5336 |
| rs532489953 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777835 | AATCTGGCCAACATA[A/G]TGAAACCGCGTCTCT | 5336 |
| rs532490980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940898 | CCCTTGCTGGATGTT[A/G]AATTTTCCTTCTTCC | 5336 |
| rs532496488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800942 | GGCACCAGCTGGCTC[C/T]GAAGATGGAGGAAGG | 5336 |
| rs532498704 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914759 | GACCTGTTCCTGCTT[A/G]TGTAACATTGGCTGG | 5336 |
| rs532499643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888528 | ACCAGGTGCTGCATT[A/G]GGCACATAACCTAAT | 5336 |
| rs532502371 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961239 | TGTATCTGTGTGAAC[A/G]AGGATCAACATCTCC | 5336 |
| rs532504426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785630 | TGCTTTGGCTATTCA[A/C]ATATTCTTTAGGATA | 5336 |
| rs532508549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885600 | GTTTGTAAATACTTC[C/T]GTATGTTTCTCTCAC | 5336 |
| rs532541676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812163 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 5336 |
| rs532551218 | in-del | -/AGATT | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900310 | TTGAACTTGAAAAAA[-/AGATT]AGAGACTTTTTTCTG | 5336 |
| rs532567900 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789851 | CCACCTTTGCCCCCC[C/G]TCCATTGCCTCCCCT | 5336 |
| rs532575397 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862618 | CTGACACCTGTAATC[C/T]TAACAGTTTGGGAGG | 5336 |
| rs532579128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925480 | AAAGGGCTTACAACC[C/T]GCAGTCCTGTGTCTC | 5336 |
| rs532602469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860624 | TGAGGTTGAGCATTT[G/T]TAATTCATTATGTTT | 5336 |
| rs532603236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811849 | GTGCATGTGTCTTTA[C/T]AGTAGAATGATTTAC | 5336 |
| rs532608873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801800 | ATTCTCTTGCTTCAG[A/C]TTCCCCAGTAGCTGG | 5336 |
| rs532614463 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912013 | CGTGTTAGCCAGGAT[A/G]ATCTCGATCTCCTGA | 5336 |
| rs532617915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853722 | TACATTTTATTGGTT[A/G]AAACAGGTCACAGAG | 5336 |
| rs532623170 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827601 | AAGCAGGTTGTATCT[A/C]GGGGACAAATGACAA | 5336 |
| rs532627243 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814407 | TTGAAAGGTACCCAT[-/G]GGGGACTGAGTGCAG | 5336 |
| rs532627278 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905939 | TGCTGAGATTATAGG[C/T]GTAAGCTTCTAAGCC | 5336 |
| rs532628962 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962014 | GCTAGGTGGGTGTCC[C/G]CTTCCTACCTCACCG | 5336 |
| rs532638303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842684 | TCAGGGGTGGGAGGA[C/T]GTTCCGTGGGTGCAG | 5336 |
| rs532652478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819725 | GAGCAGCTGGGATTA[C/T]AGGTACCCACCACCA | 5336 |
| rs532655757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868888 | GTGCCTCCTCATTGG[A/G]GCATCACTGTACGCT | 5336 |
| rs532664249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930529 | AAGGTGAGTGGATCG[C/T]TTGAGCTCAGGAGTT | 5336 |
| rs532669659 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911756 | GCTGGTATTATAGGC[A/G]CACGCCACTGGGCCT | 5336 |
| rs532678378 | snp | A/G | | | missense | PLCG2 | GRCh38.p7 | 16:81786146 | GAGACGCGGCAGGTG[A/G]CCTGGAGCAAGACCG | 5336 |
| rs532680550 | in-del | -/AAAAAAAAAAAA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792500 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GACAAAACAAAACAA | 5336 |
| rs532681072 | snp | A/T | 4.97929e-05 | 0.00498939 | missense | PLCG2 | GRCh38.p7 | 16:81957973 | TAAGAGAGAAGAGAG[A/T]CAGCAACAGCAAGTT | 5336 |
| rs532689222 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946083 | TCTCTACCCTTTGAA[C/G/T]TAGGCCTATGATCCC | 5336 |
| rs532699993 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955251 | GGTCATTAAAGGAGG[-/A]AAAAACCTTGCAGAG | 5336 |
| rs532712198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903965 | TTGGCTAGGCGTGGT[C/T]ATATGTATCTTCTTA | 5336 |
| rs532712308 | snp | A/G | 6.31898e-05 | 0.00562058 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908615 | CCCGACCCAGGGAAC[A/G]CCTACCTTCTTCTCC | 5336 |
| rs532712833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876397 | CCTAAGTACCACTGA[A/G]TGCGTAAGACCAGCT | 5336 |
| rs532725030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953909 | TTTGAACTTGCGCCC[A/G]AATAACAAATACCCA | 5336 |
| rs532726417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909982 | CTGGCTCTAGAGAAG[C/T]AGTTATATATATAAA | 5336 |
| rs532734596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782833 | TGGACATTACTGCTG[C/G]ACCTTACACCCACCC | 5336 |
| rs532735073 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933200 | CTGAGATTTCATGAG[A/G]ATGATTTTTAAAGTC | 5336 |
| rs532755621 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962630 | TTGGCTGTTGTTAAT[C/G]TGAAAATTAAACAGC | 5336 |
| rs532772760 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944820 | GCCTCCAAGGATTTT[A/G]GTATCTGGGGAGGTC | 5336 |
| rs532774375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840722 | CCTGCTCACCTCCTG[C/T]TGTGCGGCTCGATTC | 5336 |
| rs532786612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841193 | CCCCTATCTGCAGGC[C/G]AAAAAGTAAACTTTA | 5336 |
| rs532790612 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961465 | ATCCAGAGGAAAATT[G/T]TAAAGGCTTACAGCC | 5336 |
| rs532802705 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879200 | GCTCCCTCCAGATGT[A/T]AATAAGCTGGGTGTG | 5336 |
| rs532803004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876091 | GGTGCAGTGGTACAA[G/T]CATGGCTCACTGCAG | 5336 |
| rs532803878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836329 | CCCTGTATTGGCCCA[C/T]GTGTCAGCCATGGAC | 5336 |
| rs532827349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809202 | TCAGCACACACCTCT[A/G]CACACCACAAGCCAC | 5336 |
| rs532840252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817694 | TCTCACTGTGTTGCC[C/G]AGGCTGGTCTAAAAC | 5336 |
| rs532856402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862475 | CCAGAGAGGTTAAGT[A/G]ACTTGACTAAAGCAG | 5336 |
| rs532861194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840386 | CTGGGGGGATAGTGT[A/G]AGGATGATTCAAGGG | 5336 |
| rs532861235 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844409 | CAACCTCTGCACCCC[C/G]ACAATGGGTTCAAGT | 5336 |
| rs532873050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932379 | TCATTATATCAGAGC[C/G]ACATGGGAAAGTGCC | 5336 |
| rs532880037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886411 | TGTGCAAATTAGTAT[A/G]CCTTTTCTAGAAAAC | 5336 |
| rs532884350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861533 | TCTCTCCGTCCTCTT[C/T]TTCTCATCCAAAATG | 5336 |
| rs532892903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836611 | CCGGGCATGATGGCA[C/G]ACTCCTTTGGTCCCA | 5336 |
| rs532897972 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844116 | CGAGTAGCTGGGACT[A/C]CAGGTGCCCGCCACC | 5336 |
| rs532945394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855605 | GAATGGGACCTGGTG[C/G]CGCCTTTAAGAAGCT | 5336 |
| rs532950229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886854 | GGCCATCGCCATTTA[C/T]TTTTATTTTCATCCT | 5336 |
| rs532965599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914109 | GTTCAGTCCGCTGCA[C/T]ACGGATTGAAAACCT | 5336 |
| rs532975538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851826 | GCTTGTTTTCACATG[A/G]CTTTTGCCCACTGAG | 5336 |
| rs533000085 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783640 | CCGCTGCCGTATTTC[C/T]CATTGAGATAAATGA | 5336 |
| rs533017457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830007 | GTGCTGTCTTGCCTT[C/T]AAGGAGTGGAGAGAT | 5336 |
| rs533027746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867072 | TGGGGAGCATCTTGT[C/G]ATTTGAAGTCTGTGC | 5336 |
| rs533032295 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930145 | AGTTTGAGACCAGCC[A/T]GGATAATGTAGCAAG | 5336 |
| rs533033019 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802728 | AGGCATGCGCCACCA[C/T]GCCCAGCTGATTTTG | 5336 |
| rs533048775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859341 | AAATCCTCCTCCTGG[A/G]GGGAGCCTCTATTCC | 5336 |
| rs533060273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902328 | GCTGGGTGGGTTATA[A/T]ACAACAGGAACTGAT | 5336 |
| rs533061235 | snp | C/T | 4.85331e-05 | 0.00492587 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783169 | TGTGTTTCCTACTTA[C/T]GTTCCAGTGGACTAT | 5336 |
| rs533064364 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883693 | CTGGCCATCATCTCA[G/T]GTGTCACTGCCTGGG | 5336 |
| rs533065003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866710 | CTCCCAGGATGGGCT[A/C]CACTGGGCACCAGCA | 5336 |
| rs533065077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942514 | GTCTTCCATACTGAA[A/G]AAATAAACTTCACCC | 5336 |
| rs533084153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918437 | ATTATTTCTATATAG[A/G]AATTTATTTCAAAAT | 5336 |
| rs533097702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910369 | GTGCTGGGATTACAG[C/G]CATGAGCCACTGCGC | 5336 |
| rs533112204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955916 | AGAGATAATTCATAT[A/G]ACCACATATCATATA | 5336 |
| rs533118530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877619 | CCAGCAATGCTTCAA[A/G]CATTCCTCGGAGTGT | 5336 |
| rs533122813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825568 | CCAAAGTGCTGGGAT[C/T]ATAGGCGTGAGCCAC | 5336 |
| rs533132048 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899521 | AAATGAGACTCATGC[A/G]ATGCACACGTGTTCA | 5336 |
| rs533134625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926996 | GTCCCCATCAGAATT[C/G]AGCCAGCAGCCGGGT | 5336 |
| rs533139528 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882307 | GGAGTGTAGTGTTCC[C/G]TAGTGTTCCCTACCT | 5336 |
| rs533147507 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867621 | ATAAGCACTATTGAA[A/C/G]TTTCAGCTTTTGTTA | 5336 |
| rs533162204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803238 | ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 5336 |
| rs533165431 | snp | A/C | 3.43041e-05 | 0.00414136 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81923562 | CTGCCGTGGTGCCCT[A/C]ATCCACAATGTCTCC | 5336 |
| rs533176223 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890109 | AGCCATGCGAACGCC[C/T]GAAAAGACGTCTCAA | 5336 |
| rs533187785 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871127 | AACCATGACAGAGCT[C/G]TGGGCAAAATGTAGA | 5336 |
| rs533188219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829098 | ATTAATGGGGTAGTT[A/G]GTAGTTTTTATTTTA | 5336 |
| rs533194667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848994 | CAGTGGTGCCAACAA[C/T]ACCACTAATGTCCTA | 5336 |
| rs533206461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880314 | TCTCAACTGTTTTGA[G/T]AGCACCTTGGCAGAA | 5336 |
| rs533229399 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806813 | TTTTGAGGGCTTCAG[C/G]AATGGCCAGGACAAA | 5336 |
| rs533245729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832930 | AGTGGTCAGCCGATA[C/T]TTGAAGGCCTCCTGT | 5336 |
| rs533246353 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947344 | TTCTTTAGTTCAGCT[A/G]CTAGGTCTTGAGATT | 5336 |
| rs533260587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899604 | TCAACAAGTGTCCTC[A/G]CCATCTGTTGACTGC | 5336 |
| rs533271425 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790272 | CTTAGGGGTTTGGAC[G/T]GGAGGGGAGTAGGGT | 5336 |
| rs533283982 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81783318 | TTATTATTATATTAT[C/T]ATTATGCTTTAAGTT | 5336 |
| rs533298738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799786 | TTTTAGTGGAGATGG[G/T]GTTTCACCGTGTTAG | 5336 |
| rs533299711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864798 | GTGATGGCTGCCTGG[A/G]TGCGGGAGTTGAAGA | 5336 |
| rs533300322 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859030 | GTTCCAGTTCCTTTT[C/G]TGCACATTCCGTAGG | 5336 |
| rs533301772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810454 | TATTTGCAACCTGCA[A/G]ACCAGTAGTTCTGGC | 5336 |
| rs533306885 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963022 | TAGGCTCCCTAGAAC[C/T]GTCAATCACTGCGTT | 5336 |
| rs533313256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792303 | CCTAGCCAACATGGC[A/G]AAGCCCCATCTCTAC | 5336 |
| rs533331015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864439 | TACCTCAGACAGCAC[A/G]GATGTCTCCATCATT | 5336 |
| rs533341728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822634 | TGGTGGCGTGTACCT[C/G]TAATCCCAGCTACTC | 5336 |
| rs533384310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915398 | TGTTGAGTTGTTGCC[C/T]GGCTGTGATTGGTGG | 5336 |
| rs533385100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895631 | TGCACTTGCATTATG[C/T]AAGCGCACAGGGAAC | 5336 |
| rs533399371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814957 | CTGACTAAACGTCAG[C/G]TGCTGGAGATGGTGG | 5336 |
| rs533419372 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855381 | CAGTCCTAGAATTTA[C/T]TGACTTAGAAGTATA | 5336 |
| rs533425803 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864778 | CTGCCATCCTTAATG[A/G]TTTGGTGATGGCTGC | 5336 |
| rs533437000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939625 | ACACCTCCCCCGTTC[A/C]CTTGTCCCTGATCCT | 5336 |
| rs533446751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943832 | ATATTCAATGAGAGC[A/G]ATGTCCCCATAAACC | 5336 |
| rs533450531 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792744 | TACTCACTATCACGA[C/G]AACAGCATGGAGGTA | 5336 |
| rs533451032 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867853 | CAGGCGCCTGCTACC[A/C]TGCCTGGCTAATTTT | 5336 |
| rs533451161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820863 | TGACGTCAAATGATC[C/T]GCCCACCTCAGCCTC | 5336 |
| rs533459559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814543 | ACTAAAACAATACGA[A/G]AATTAGCCAGGCATG | 5336 |
| rs533461443 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959772 | GCCTTTGGCCAGGTA[A/G]CCACCAGAACCTATT | 5336 |
| rs533470853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826086 | TTGTCACCAAAACAA[C/T]GGAGATCTCTGCCTT | 5336 |
| rs533488305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874652 | GCTATTTATGGTGAC[A/T]TATAATCCCCAGAAC | 5336 |
| rs533503963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956197 | ACTTAGCATAATGTT[G/T]TCAAGGTTCATCCAC | 5336 |
| rs533504122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951521 | AATAACGTAATTCCA[A/T]TTTCACTCCACCAAA | 5336 |
| rs533512237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851626 | CAGGCGATTCTTCTG[C/T]CTCATCCTCCCAAGT | 5336 |
| rs533538505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788846 | ATTGGCCGGCTCCAC[C/T]CCCAGGTGGCCCAGA | 5336 |
| rs533551034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859779 | CTGACCTTGTGATCC[A/G]CCCACCTTGGCCTCC | 5336 |
| rs533554861 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880196 | TGGTGAACTATGGTC[G/T]TGCCACTGCACTCCA | 5336 |
| rs533563875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905609 | CCTGTCTTGTTCCCA[G/T]TTTTAGTCAAGTGAG | 5336 |
| rs533564031 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844229 | CTATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 5336 |
| rs533565755 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868100 | GATTCAAATCCAGGC[C/T]CTGCTGCCTGCCATC | 5336 |
| rs533573341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955227 | GTTACCCTGGGGACT[C/G]TTTTGTTAGGTCATT | 5336 |
| rs533582847 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950816 | GAAGAGGAAAGTGCT[G/T]GCCTTAAAACTTCAC | 5336 |
| rs533617367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859051 | ATTCCGTAGGACTCA[C/T]TTAGACTTGTGCTAT | 5336 |
| rs533622850 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780990 | CCAGATCATGCCACT[A/G]CACTCCAGCCTGGGT | 5336 |
| rs533640216 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832619 | GTGTTGCCCAGGCTG[G/T]TCTTAAACTGCAGAG | 5336 |
| rs533643036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883426 | CTGCCGCCTGTGCTC[A/G]CCTGGTCACCTGTGC | 5336 |
| rs533646951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782877 | GGGATACAGTGTTTT[A/C]AAAGGAACGGTGTCA | 5336 |
| rs533670037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788076 | TTATTTGTTTTGGGT[A/G]TATACCTAGGAGTGG | 5336 |
| rs533674114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887771 | AGAAAGCATTGATCA[A/G]AGTTGAATTTACATG | 5336 |
| rs533676091 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905285 | TAAGAGGGAAGCCAG[G/T]CAGCAAGAACAGGCA | 5336 |
| rs533682302 | snp | A/T | 0.0023933 | 0.0345097 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962712 | GCCCAGAACTTTTTT[A/T]AAAAACTGCTATTCA | 5336 |
| rs533685842 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910028 | GGTGGGGTGGGGGAA[C/G]TAGGTAGAATGTTCT | 5336 |
| rs533700490 | snp | C/T | 0.000149089 | 0.00863264 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81891525 | GGATGAGAAGTATGA[C/T]GCGGTGGACATGCAG | 5336 |
| rs533716624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915063 | GGGTATGGGGTGAAG[C/T]GTCACTGTCCTTCAC | 5336 |
| rs533721207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943076 | AGATAGTACTGTCCA[A/G]CCTGGAACCATGCTA | 5336 |
| rs533743611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918788 | GTCAAAAATATTTTT[C/G]CAGATGTTTCTGTCT | 5336 |
| rs533752896 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923316 | CTGGTGGCTTTTTGG[G/T]GCCTTCGATCCTTTG | 5336 |
| rs533753096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833121 | TGCTGGCACCCACCT[C/T]GCAGAACCCATTCCT | 5336 |
| rs533802481 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959329 | TTAGTATGCATGTAC[C/T]GCTGAAAAGCAGGGC | 5336 |
| rs533803101 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778613 | GTCTGGGGTTCTTTG[C/T]TCCTGACTCCCTTTG | 5336 |
| rs533826442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951588 | AGCTATACAACTTTC[A/G]TATCAAAACTGGAGA | 5336 |
| rs533830504 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899347 | ATATATGTATATACA[G/T]GTACTAATGATATGT | 5336 |
| rs533874683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879972 | ATACTAAAGATTTGA[A/G]ATGTTGCCTGTAATC | 5336 |
| rs533876743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803267 | GGGACTACAGGTGCC[A/C]ACCACCACGCCTGTC | 5336 |
| rs533877385 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952228 | TGTTGGATTGGAATT[A/G]GAGGTATCAATATAA | 5336 |
| rs533880859 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892098 | GCAGGTGGTAAGGCA[A/G]GGAGAAGTGTTTCAG | 5336 |
| rs533893265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810243 | GGCATGCCTCAGCCT[C/T]CCGAAGTGCTGGGAT | 5336 |
| rs533894172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910966 | TTTGTCTTCATAGCC[C/T]CGAGACTTTGGGCTT | 5336 |
| rs533919239 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883191 | TGGGTGGCAGGCTGC[C/G]CCATTGGCTGGCATC | 5336 |
| rs533935348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810884 | ATTTTGTACATGACT[A/G]TATTTATAACGAAAA | 5336 |
| rs533965525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935191 | GGCTGTGCTCCCTCC[A/G]GAGGGGAAAGCCATT | 5336 |
| rs533993522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814590 | ATCCTAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 5336 |
| rs534006636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831026 | GCCTTTGCATTTACT[A/G]TTTGCTCTGCCTGAA | 5336 |
| rs534010556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844714 | TTGCATAAAAAAAGA[C/G]TTAATAAGTTATAGT | 5336 |
| rs534015333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792391 | GGAGGCTGAGGCACA[A/G]AATTGCTTGAATGTG | 5336 |
| rs534026857 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841267 | ATTGAGATAGAGTCT[C/G]ACTGAGTCGCCTAGG | 5336 |
| rs534031694 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81819511 | CTGCTTTTCACCCTG[A/C]CCTGAGGTGTGAGAT | 5336 |
| rs534055974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894966 | CGACTCATCATGGAA[A/G]CAACGTTTTGTAGCA | 5336 |
| rs534056780 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914776 | GTAACATTGGCTGGG[A/G]TGTAGTTGGTGGTTG | 5336 |
| rs534057736 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867657 | GTTACTGCTGCTGCT[G/T]CTCCTTTTGCCTGGG | 5336 |
| rs534059730 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81881110 | ATCCCATGCCTGTGG[C/T]GTGGATAGAGATGAG | 5336 |
| rs534060649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923069 | TGGGAGGCTTGCTGA[A/G]CACCGGCACTGTGAT | 5336 |
| rs534061879 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845232 | AGGCATGAGCCATTG[G/T]TCCCTGTCCCGTGTT | 5336 |
| rs534063424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947094 | CAGCATTTGCCTAGG[C/G]CCGCTGCTCTGCAAG | 5336 |
| rs534072519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796412 | GCTGCTTTGGAGATC[A/G]GTATCCTTTGGCACG | 5336 |
| rs534090369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956946 | TGATGATGGGCACCA[C/T]GGGCCAGGCTTCTGG | 5336 |
| rs534102678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826515 | TAGGACCTATCTCAC[A/G]GCAGTGTTTTAGAAT | 5336 |
| rs534129784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799539 | AAGAGATCCTCCCAT[C/T]TTGGCCTCCCAAAGT | 5336 |
| rs534130322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878074 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 5336 |
| rs534142171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833572 | TTTCACTCTGTCACC[C/T]AGGCTGGAGTGCGGT | 5336 |
| rs534145658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899033 | TCTTTAGTAAAAATA[C/T]AAAAAATTAACTGGG | 5336 |
| rs534151218 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955669 | TGACTCAATAGCAAC[A/G]TGGCCATGACAGGAC | 5336 |
| rs534166372 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959811 | CTGGCATCTCCCCCA[A/G]CCCCTCTCAGCTCTG | 5336 |
| rs534181375 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852754 | ATTTCTACAATCTGG[A/G/T]CATGGGTGGGGACTG | 5336 |
| rs534186552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779809 | CCCTTGTGCCCAGAG[C/G]TCGCGGACGCTCGGA | 5336 |
| rs534191173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803905 | CAAGCTAGTCTTGAA[C/T]TCCTGGCCTCAAGTG | 5336 |
| rs534198070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856168 | TGAGACAAACTCAGC[C/G]CTTCAGAGCCTCAGT | 5336 |
| rs534199104 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887802 | TCATATTTCATCCCC[A/T]TTTCCTATGAATATT | 5336 |
| rs534205537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837198 | TGCAGTGCTGCTTCA[G/T]ATGGAAGTCAGAAAA | 5336 |
| rs534211297 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883926 | GCCCCCAGAGGACAC[C/T]GGGCAGTGTCCAGAG | 5336 |
| rs534215543 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808077 | TTCTACCTTTTGGCT[A/G]TTATGAATAGTGCTG | 5336 |
| rs534232842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859826 | CAGGCATGAGCCACC[A/G]CGCCCGGCCACCAGG | 5336 |
| rs534234858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887411 | GGCATGAGCCACCAC[A/G]CCCGGCCTAGTATTT | 5336 |
| rs534281811 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943668 | TTTTAACAAGATTCA[C/G]AGGTGATTCACATTT | 5336 |
| rs534299790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812337 | TACAGGCGTGAGCCA[C/G]CGCACCCGGCCTGTT | 5336 |
| rs534304151 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780887 | CAAAAATTACCTGGG[C/T]GTGGTGGTGGCCGCC | 5336 |
| rs534309516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861218 | TGATTTATTTATGTC[A/G]TTATCCTATGTGGAT | 5336 |
| rs534312159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943315 | AGGCCTCAGGAAATT[C/T]ACAATCCTGGTAGAA | 5336 |
| rs534322372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814192 | CAGCGGAGGGGAATG[C/G]TACCGGGTCTGAAGG | 5336 |
| rs534335980 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835930 | TCCCTCTTACAAGGA[C/T]AGTAGTCTTGGGTTA | 5336 |
| rs534340041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885486 | CCAGTTTTATTTCAT[C/G]CACTTCTAACTTTAC | 5336 |
| rs534353936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899775 | CGCTTGGTTCAGGCA[C/T]GAATTACAGTGATGC | 5336 |
| rs534357828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952313 | TGTGTGTTTACATGT[A/T]ACTACAAATACATAC | 5336 |
| rs534360627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811982 | CTGATTTACACTCCT[A/C]CCAACAGTGTAAAAG | 5336 |
| rs534369043 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824096 | GTCCTGTCCTGTCCT[G/T]TCCTTTCTTTCCCTC | 5336 |
| rs534378356 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857184 | GTGTTTCCACCTGTT[C/G]ATGTCTCCGTCATCC | 5336 |
| rs534380658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923784 | AATGGATAAACAACA[A/G]TATTAACAGGTATCG | 5336 |
| rs534395713 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794143 | ATCCTAGAGGCGCCG[A/G]ATTTGTGGGGAGATG | 5336 |
| rs534414545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941221 | AGTTTCTGAGCAGCA[G/T]GCATGCTAGAAAATC | 5336 |
| rs534424237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815907 | TTTTTACTAAAAATA[C/G]AAAAATTAGCCAGGC | 5336 |
| rs534424912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865175 | GGCCAGGCCTTTGTT[C/T]CCTTGCGTGGACTGG | 5336 |
| rs534430457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945147 | CTCTTCATAAGCAGC[A/G]GAAAGTGAGAGATTC | 5336 |
| rs534467405 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847637 | ATTTGTGGATTCTGC[A/G]TCTGCGGATTTAAGC | 5336 |
| rs534471272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903008 | TCCTATGACACGTGG[A/G]AATTATAGGAGCTGC | 5336 |
| rs534477781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954153 | TCAGCCTCCTGAATA[G/T]CTGGGAGTACAGGGT | 5336 |
| rs534492577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833868 | TGTGTCTTGCCTAAC[A/G]ATTGCCTTTGGCGAT | 5336 |
| rs534499570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925581 | CCACCACGGAGCACA[C/G]ACTTGATTAAGATCC | 5336 |
| rs534507430 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926643 | CACTCACGTTTATGC[A/C]TTTTTCAGATGGAGA | 5336 |
| rs534511957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879349 | CCCCTTTTTAAAAAG[A/G]AATACCTATGCTGTA | 5336 |
| rs534531283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884374 | AAAAACAAAAACACC[C/T]CCACCCCACCAAAAA | 5336 |
| rs534537335 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958220 | ATTCTTTATAGAGGA[A/T]TCCCCAAAATGTGCT | 5336 |
| rs534538361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880560 | GCAGAATAATATGTA[A/G]AGCTTGAAACACAGC | 5336 |
| rs534541882 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960113 | AAAACTGTCTCCTTC[A/T]CCTGGTGCTACAACC | 5336 |
| rs534558918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835282 | CGTACAGCTAACACT[C/T]AGTAAGTAGCTGTTA | 5336 |
| rs534559853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929000 | TCTTGGGTTCTAAAC[C/G]CAGCTCTGCCTCTCT | 5336 |
| rs534564095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809380 | GTCAGGACACTCCTG[C/G]CTTGTTCTGCACTGA | 5336 |
| rs534569919 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785815 | AGCGATGCCTTGCCA[C/G]TAGAACCTTCTCCTA | 5336 |
| rs534570423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805381 | TCGGGTGCCTATAGT[C/G]CCAGCTACTCAGGAG | 5336 |
| rs534576940 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848753 | AGGGGTGGAGCTCAG[A/T]GGTGAAGAAGGGTGT | 5336 |
| rs534581346 | in-del | -/TTTTA | 0.00120361 | 0.0245022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808481 | ACCACTGTGCAATCT[-/TTTTA]TTTTATTTTATTTTA | 5336 |
| rs534604852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861619 | TGAGGTGCTTGTGTT[A/G]GAAGATTTGGTACAC | 5336 |
| rs534606329 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912823 | CCTGCAGTGCCCTGC[A/C]CCCCCAGCATCAGCG | 5336 |
| rs534615011 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788412 | CAGCCTCCCGAGTAG[C/G]TGGGACTACAGGCGC | 5336 |
| rs534615656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857289 | GAGCAGCTGGGGTTG[A/G]GAAACTCTGCTCTGG | 5336 |
| rs534625475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937431 | CATAGATGTATCAGA[A/T]CTAAGAGGTTAAAAA | 5336 |
| rs534631703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789945 | TGGATTCAAATCTCC[A/G]TGGAGCCTATATTGC | 5336 |
| rs534642222 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882266 | CTGGTGGCCTGCTGG[C/G]CAAGGCGGGAGTCCT | 5336 |
| rs534651891 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900239 | TCCCTGTTGGTGACC[C/G]TGGGTGAAGCACACA | 5336 |
| rs534658079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816124 | GCCGGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 5336 |
| rs534667270 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854084 | CTCTAGTGAGCATCA[A/G]TTTGGTCTCTTGTTT | 5336 |
| rs534672770 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777648 | AATGAATCCACAGAT[C/T]TTGTGAAGTCACAAA | 5336 |
| rs534686740 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949408 | TGTGTATAAAGGAAA[C/G]TGAATAAGTCTAATA | 5336 |
| rs534714184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798890 | CGGCTGGATTTCACC[G/T]GCCAGGTGTCTCTCT | 5336 |
| rs534719565 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850358 | CAGATAAATGAAACA[A/G]ACAAACAAAAAAGTT | 5336 |
| rs534741251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824707 | CGTAGCTGCCATGTG[A/T]CCTCTGGCCTTTTTG | 5336 |
| rs534741263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820616 | TGTATAATGGGGAAA[C/T]ATTACCCAATTTTTT | 5336 |
| rs534743540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846823 | GAGAAAGGAAAAATC[A/G]AGGTGTGTTTTTTTT | 5336 |
| rs534747933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869512 | AATAAAGACCATGTT[C/T]ACTGAGCTCTTGGAC | 5336 |
| rs534748980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820137 | TAAGAACTTTTTAAA[A/G]TGAACTTTATTTCAT | 5336 |
| rs534755048 | snp | A/C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851615 | CCTCCCGAGTTCAGG[A/C/T]GATTCTTCTGCCTCA | 5336 |
| rs534761367 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81898168 | TCGAACATTATCTCA[G/T]TCATGACTAGAGGAA | 5336 |
| rs534775246 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958656 | ATGGAGGGTAGGAAT[C/T]TTGGGGCCTCTTTGT | 5336 |
| rs534800483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824479 | CAAACAGCCTCTGGG[G/T]TTGTGACTGCTGGAA | 5336 |
| rs534817193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828347 | GCCTCCCAAGTACAC[A/G]CCATTCTCCTGCCTC | 5336 |
| rs534845546 | snp | A/C | 1.65658e-05 | 0.00287795 | missense | PLCG2 | GRCh38.p7 | 16:81854457 | AGTGGATATCATGGA[A/C]ATAAAAGAAATCCGC | 5336 |
| rs534847563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782025 | TACAGGCATGTGCCA[C/G]CACACCCGGCTAATT | 5336 |
| rs534850143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836364 | ATTCCCACTGGTGGA[A/G]CCAAGAGGTTTTTGC | 5336 |
| rs534869556 | snp | C/T | 1.9383e-05 | 0.00311306 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921337 | GGATTCCATCTTGTT[C/T]CCATGGCAGTTATAA | 5336 |
| rs534870233 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962307 | TTTTTGAACCCAACC[A/G]TAAAAGCTATCTTCT | 5336 |
| rs534880756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857685 | CATGGAGGCCCCACT[C/T]TCATTACTTCATCTA | 5336 |
| rs534881761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853875 | GGCCCTGTGATATCC[A/G]GAACCCCTGTTACCA | 5336 |
| rs534908694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840527 | TCCTGCAACTAGACA[A/G]TTCTATCTGGGAGTG | 5336 |
| rs534915319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835570 | GGCGACAGAGCAAGA[C/G]TCGGTCTCAAATATA | 5336 |
| rs534920953 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909285 | ACATCCCTCCCTTTA[C/T]TGGGGGGGTTTAATG | 5336 |
| rs534937868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886223 | TACGTGCTTTCCCCA[A/G]ACGGGGCCCTTTGCT | 5336 |
| rs534940746 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826879 | TTTTAAAAAGTTCTT[C/T]TTCTGTATCCATTTG | 5336 |
| rs534941647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890362 | AAAGTTAGCTTGGCC[C/T]AAGCCCAGGAATAAT | 5336 |
| rs534946156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885802 | GGCTCAGGAAAGGGT[C/T]GTAGCTACCCTAGTA | 5336 |
| rs534948918 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817443 | GCTTTTGTTGCGCAC[A/G/T]CTGGAGTGCATCGTC | 5336 |
| rs534954137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908754 | AAGGGTGAGGTGGGT[A/T]TGACTCACTTCGGCA | 5336 |
| rs534958574 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961715 | AAAGATCATAGTATC[G/T]ATCAAATAACTTATA | 5336 |
| rs534968342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869937 | GAAATGAGCAACCCT[G/T]CATCCAAACAGCCCC | 5336 |
| rs534995498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894054 | GGCAAACAGACACCC[A/G]CTGTGTTTTGGCAGC | 5336 |
| rs535021252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922021 | AAGGATGTTTTGGCG[A/C]TGAGAACAGTCACCT | 5336 |
| rs535024235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889904 | TTGTGATCAGCCCGC[C/G]TCAGCTTCCCAAAGT | 5336 |
| rs535027303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794753 | GCTGTCGTTGATGTC[A/T]TCATTATCATCATCC | 5336 |
| rs535028052 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886180 | TGGGGCGTGTAGATT[A/T]ACCCCACCTAGTGGT | 5336 |
| rs535048489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894302 | TGTGTAGTGGCATGC[A/G]CCTGTGGTCCCAACA | 5336 |
| rs535076790 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838047 | ACCAATTCCATTTCC[A/G/T]AAATTTTAACATGTC | 5336 |
| rs535078095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879364 | AAATACCTATGCTGT[A/G]AATTACACATCAACG | 5336 |
| rs535081129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862084 | CAAAAGAAACTTTGA[C/T]CAAGATGCCAATGAA | 5336 |
| rs535100514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913178 | GTTCTCTAATGTTAC[A/C]CCAAAACGCCAGATT | 5336 |
| rs535106283 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929426 | TTCGCGATAGAGTCT[C/T]GCTGTGTCACCCAGG | 5336 |
| rs535123548 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908783 | CACTGTAACCCAGAT[A/T]AATGAGATTTCAGGG | 5336 |
| rs535128483 | in-del | -/CCC | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963128 | TGGTTGGATTAGTTA[-/CCC]TGGTCCAAAGATTTA | 5336 |
| rs535159845 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963095 | TCATACCTCTGACCC[A/C]CAACCCCCAGCCCCC | 5336 |
| rs535166685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790510 | TCTCCTGCTGAGAAG[A/G]GTGACGTTTTATCTC | 5336 |
| rs535168117 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851118 | ACCCCACAAGGTTTA[C/G]AGATACCACCCCCCT | 5336 |
| rs535188613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785841 | TCCTAAAACTCATCC[C/T]GATTGACATGAGACA | 5336 |
| rs535198090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912837 | CCCCCCCAGCATCAG[C/T]GACAACAACAACCAC | 5336 |
| rs535204236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843338 | TCTCACACCTTTACA[C/G]TCATACGTGCACACT | 5336 |
| rs535218170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909624 | GTCTCACTACGTTGC[C/T]CAGGCTGGTTTTGAA | 5336 |
| rs535219422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862535 | TGCAGACTTACTTTC[C/T]CCACTGGTGTTGCTT | 5336 |
| rs535220858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812344 | GTGAGCCACCGCACC[C/T]GGCCTGTTGTTTACT | 5336 |
| rs535224592 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81863475 | CTTGAGTTGCTTCCA[C/T]GTTTTGGCAATTGTG | 5336 |
| rs535242284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882554 | AGCCCTGTCTGGGTA[C/T]TGGATAGGCACACTC | 5336 |
| rs535251794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950379 | TTCTAAAGGGATATA[A/T]AAGTCATTAGCAAAT | 5336 |
| rs535252690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938373 | TCCTAAGGTTAAGGG[C/T]GGGCGGGTGGTAGGG | 5336 |
| rs535274265 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922526 | TTAGTAGTCTTAACA[A/G]CCCTGTGAAATATAT | 5336 |
| rs535274797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802497 | AGTAGATATGTGATA[C/T]TGAATGTGTAACTGC | 5336 |
| rs535280174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813244 | GGAATAGCATTGAAT[C/T]TATAAATTACTTTGG | 5336 |
| rs535314291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929580 | TTTGTATTTTTAGTA[C/G]AGCTAGGGTTTCGCC | 5336 |
| rs535321057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942574 | AAACCAGTTGGAGCG[C/T]AGGAAGGAAAGCAGC | 5336 |
| rs535328799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802269 | AGGCGCCCGCCACCG[C/T]GCCCAGCTAATTTTT | 5336 |
| rs535346566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817037 | GTTAGATGCTGGGGA[A/G]ATAGAGGCACAACCA | 5336 |
| rs535347890 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800813 | CTCCTTGCAGATTGA[A/G]CAGATCTTGAGATGG | 5336 |
| rs535347942 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814305 | TTTTAGCAGTGCTTC[A/C]GGAGCTGAGACAGGG | 5336 |
| rs535356782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843858 | CCGGGTTTGATGTGC[C/T]GTTGGTTGTGTGTCT | 5336 |
| rs535364015 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866429 | CCAGGATGAGCTCCA[A/C]TGGGGCACCAGCATG | 5336 |
| rs535390015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795101 | GATGTGTGTTGGGCA[A/T]TGTGCTTGTCACTGG | 5336 |
| rs535394272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831666 | GCATTTGTACCCCGA[A/G]TGGGACTCAGATCCT | 5336 |
| rs535412103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809826 | TCAGGATTTTTTGGC[C/T]GGGGCGGGGGGTGGG | 5336 |
| rs535421201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809505 | CCACCACCCCATTCC[C/T]CTTGCAGTGATTCCT | 5336 |
| rs535425449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790347 | ATCTTTGAGCATGCA[A/G]TGGAGGTCCTGTTTG | 5336 |
| rs535449162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946977 | GTGCATCTATTGCCC[A/G]GGGAAAGGGAACCAG | 5336 |
| rs535452463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882572 | GATAGGCACACTCAC[A/T]TCCCTGTGTTCCCCA | 5336 |
| rs535458221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886090 | AGTTTAGTAGGGAAC[C/G]ATTAAAGTTAAATTG | 5336 |
| rs535463300 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821795 | TGCATAACTTCCTAC[C/G]CAAAAGAAAAGGTTT | 5336 |
| rs535466400 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961806 | GTCTACGGTATGCCA[A/G]CACTTTGCAGCTATT | 5336 |
| rs535469162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918611 | CACTGGTCTGTGTGT[C/G]TGTTTTTATGCCACT | 5336 |
| rs535477641 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865526 | GCTTGGATGCTCAAG[C/T]CCCTGGTTCCTGGGT | 5336 |
| rs535481389 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828834 | GTGAATTTATTTCCC[C/G]TTAACTTGCATTCCT | 5336 |
| rs535489228 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802021 | AAAAAATCTGTGGCT[G/T]TGCAGAGGTGCCCAC | 5336 |
| rs535492922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812722 | TTTGCCATTGCTTTT[G/T]GTGTTTTAGTCATGA | 5336 |
| rs535495636 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795543 | GTCTGATCACAATGG[C/G]ACTCTGTGCTATCAT | 5336 |
| rs535506369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817100 | GGTGGGGAGAGACGG[A/G]TGGTAAACAGGGAGG | 5336 |
| rs535535276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874041 | TGTATGGCAAAGATT[C/T]TGCCGATACCAAAGG | 5336 |
| rs535546070 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941774 | TGATCTCGGCTCACT[A/G]TAACCTCTGCCTCAG | 5336 |
| rs535557819 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865839 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGGTGAGCT | 5336 |
| rs535563001 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805059 | CAAAGTTTTCAGAGG[-/AAC]AACATCAGACACTTT | 5336 |
| rs535563729 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876199 | CAGGCTAATTTTTGT[A/G]TTTTTTGTAGAGACA | 5336 |
| rs535573847 | snp | A/G | 0.000198039 | 0.00994889 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889291 | GAGTAGGCTGGGCTT[A/G]TTGTCGCTTGGGGGT | 5336 |
| rs535595083 | snp | A/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962521 | AAGCTGCATTTGTAA[A/T]CTTGTGTTTCATTAT | 5336 |
| rs535610548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898269 | AATGCATTAATGTTT[G/T]GGCAGCAAAAGCCAT | 5336 |
| rs535610675 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902053 | TTCCAGCTCAGAGCA[C/T]GGGAAGTCCAAGGGT | 5336 |
| rs535620293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851423 | TTCTACGAAATCTTG[C/T]CACGTGTAGGTGGGT | 5336 |
| rs535628985 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877838 | GATGTCATTGCATCG[C/G]TCCTTGGCTTGTAGA | 5336 |
| rs535638682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783337 | ATGCTTTAAGTTTTA[A/G]GGTACATGTGCACAA | 5336 |
| rs535642542 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959380 | CAGAAGATCCTTCTG[A/G]TCCCTTCACTCTACA | 5336 |
| rs535643257 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876977 | AATTCTGGCCCTTGG[A/T]CTTGTTAGGAGAAAA | 5336 |
| rs535657347 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963133 | GGATTAGTTACCCTG[A/G]TCCAAAGATTTAATA | 5336 |
| rs535662993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883481 | GGCCACCTGTCTTCA[G/T]GGAACGATTGCAGTC | 5336 |
| rs535668483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832695 | AGGCATGAGCCATTG[C/T]GCCCAGGCAGAATCT | 5336 |
| rs535669088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810527 | TGGGTCACCCATTCA[C/T]ACATGCCCTGCTGAG | 5336 |
| rs535669824 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853828 | TACTCTGGACTGTTA[C/T]CAGAGTCATAGTTTA | 5336 |
| rs535680473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828385 | TGGGACTACAGGTGC[C/G]TGCCACCACGCCCGG | 5336 |
| rs535688781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836731 | AGCAACAGAGCAACA[C/G]TATGTCTCAAAAACG | 5336 |
| rs535696867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802040 | AGAGGTGCCCACCAA[C/T]ATTCTGTCTGGAATG | 5336 |
| rs535704551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863061 | AAACATAGAACAACA[C/T]TGATCATTTTAACCG | 5336 |
| rs535715020 | snp | C/T | 0.000530038 | 0.0162708 | missense | PLCG2 | GRCh38.p7 | 16:81854573 | AGTTCGTCCTCAGCA[C/T]GCTCAGCTTGGCAGG | 5336 |
| rs535717978 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923690 | AAGTCTGACCCCCTT[G/T]GTCATCCTGGGCTGG | 5336 |
| rs535742762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886974 | TCAGTCTTCTTTAGG[C/T]AGAAGATTTCTTTCT | 5336 |
| rs535744756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883214 | CTGGCATCTCCTCTC[A/G]ACTCCTCTGTTGAAT | 5336 |
| rs535770440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813611 | AAACAACAATTCTGT[C/G]GGTCAGGAATTTGGG | 5336 |
| rs535779468 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904707 | TGTCTGCTAAGTGCT[C/T]TTCTAGCACAGGAGA | 5336 |
| rs535785250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939250 | ACACAGAGAGAGGGG[A/G]TGAACCTACGTGGCT | 5336 |
| rs535806453 | snp | C/G/T | 3.88765e-05 | 0.00440871 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921338 | GATTCCATCTTGTTC[C/G/T]CATGGCAGTTATAAC | 5336 |
| rs535810022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890730 | AATTAGGCCCAGATC[A/G]CTAAAGCATTTTTTT | 5336 |
| rs535817608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948759 | GTTTGCCTAATGCTG[A/G]CTCCAAAGAGCAAAA | 5336 |
| rs535840031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913849 | TTTCCCTTCCTCCTT[C/G]CCTGCACCACTATGC | 5336 |
| rs535845623 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918153 | TTCTGTAGGTTGTTT[A/T]TTTACTCTGTTGATT | 5336 |
| rs535874535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920057 | TAGCATGCGCAAAGG[G/T]CCTGAGGTAGAAGCC | 5336 |
| rs535893190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818643 | CAGAGCCAACTAGCC[A/G]GGCATACCTTTTCTC | 5336 |
| rs535903297 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846446 | AGGCTCAACTTCCAG[C/G]GAACCAACCTATGAT | 5336 |
| rs535907332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847763 | TTTACATAACATTTA[C/T]ATTGTATTAGGTATT | 5336 |
| rs535908252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871845 | AAAGTACCTGGGCAC[C/T]ATCTGAATGTCTCAA | 5336 |
| rs535909725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843873 | CGTTGGTTGTGTGTC[C/T]AACTGCTTCTCTTCC | 5336 |
| rs535917412 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81817442 | CGCTTTTGTTGCGCA[C/T]GCTGGAGTGCATCGT | 5336 |
| rs535930136 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896361 | GAAACCCCTTCTCTA[C/T]CAAAACACACACACA | 5336 |
| rs535937693 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833842 | CATGAGCCACGGCGC[C/T]CGGCCTCCTGTGTGT | 5336 |
| rs535983418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947976 | TTTCTACTTCACAGA[C/T]GACTTTAAATGATTT | 5336 |
| rs535988501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834910 | AGCCTTGGTCCATTG[C/T]AGAACTGGGTACTAC | 5336 |
| rs535997108 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890712 | TCGTTCTCACGCAGC[A/T]GAAATTAGGCCCAGA | 5336 |
| rs536004228 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882389 | TTTTGCCCTGATGGC[C/G]TGGAGTCTGGTGGGG | 5336 |
| rs536007224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952913 | AAAATAGCAGCTTTA[C/T]AGCGGATAGACCCTG | 5336 |
| rs536012555 | snp | A/G | 1.66048e-05 | 0.00288134 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891436 | CCATCCTGCCCGTCA[A/G]CGTGATGATTCGGTC | 5336 |
| rs536036270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806590 | GGAGTCTGCACCATT[A/G]CATGATCATAGGATA | 5336 |
| rs536056754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885126 | CTCTGTCCCATGTTC[A/G]AGTGATTCTCCTGCC | 5336 |
| rs536062533 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878855 | TGGCTCTTGGCTTTC[A/G]TTTGTTCTTTTTCAT | 5336 |
| rs536062817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834441 | CTGGCAGGACTCAGA[A/C]CCCAGCTTGCCCAAC | 5336 |
| rs536074152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910095 | CTGCATCTGGTTTTG[C/T]TGTTGTTGTTGTTGA | 5336 |
| rs536074522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782944 | CCTTTAGGGCAACCT[A/G]TGAGCAGCTATTACA | 5336 |
| rs536090369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858672 | ATTTAATAAGAGATT[C/T]AGTGGACTGATCAAA | 5336 |
| rs536095432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888598 | CAATGCTTCACAGAA[A/G]CTGTGTGGTAGATAC | 5336 |
| rs536095473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884737 | AGAGTTTATATTTTA[C/G]AGTAGTTTTAGGGTT | 5336 |
| rs536097375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810296 | AGCCCATGCTTCTCT[C/G]CTATCCCAGACGACT | 5336 |
| rs536126219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836413 | CTTTGGATCTTGGCT[G/T]CTCGTTTCATCCTTC | 5336 |
| rs536129023 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892368 | TACAGGATGTTGCGC[G/T]GATGTTCCAGTATTT | 5336 |
| rs536131041 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822677 | CAGGAGAATCGCTTG[A/G]ACCCGGGAGGTGAAG | 5336 |
| rs536148558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944680 | GGGGTCTTGCTATGT[C/T]GCCTAGGCTAGTCTT | 5336 |
| rs536165254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862578 | TTTTTCTTTTTTTAA[A/C]TGTGCTACTGGCCGA | 5336 |
| rs536165318 | snp | C/T | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779122 | GCAGAGGCGGGGCTC[C/T]AGGCCTGGGCCGCTC | 5336 |
| rs536172674 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886919 | GTGCAATACCCTACA[-/C]CAAGTGGATGCATTT | 5336 |
| rs536175526 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868295 | CATGTAGGCCTTGTT[C/T]CTTCCCACTTCCCCT | 5336 |
| rs536176117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815636 | ACACAAGTCCCTCTT[C/T]AGCTGCTGGGAGTCT | 5336 |
| rs536179500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840580 | CAGGCATTAGATTCT[C/T]ATAAAGAGTGTACAA | 5336 |
| rs536180255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952497 | ATAAAAAGGACCTGG[A/C]GCATCTTAACATTTC | 5336 |
| rs536182361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914241 | AAGCGGTGAGACAGC[C/T]CTGACACAACCGGAT | 5336 |
| rs536187779 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894833 | AGCTGAGATCGCGCC[A/G]CTGCACGCCAGCCTG | 5336 |
| rs536208190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901051 | AGGGAAGGCGTGCAG[A/G]ATGCGTGCAACTGCG | 5336 |
| rs536209096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953644 | AAAAGAAATCCAGGA[A/G]ATAAGTATCACAAAA | 5336 |
| rs536224694 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871727 | GAGGGTGTATGTTTT[G/T]ATCTGACAGTGGCAT | 5336 |
| rs536225512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823745 | ATGTTGCCCAGGCTG[A/G]CCTTGAATTCCTGGC | 5336 |
| rs536228804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850280 | TGTGCTCATTTTTTT[G/T]AGATAAATTAAGTAT | 5336 |
| rs536229419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925218 | CCCAGCGGCTGTGGT[C/G]AATTCCTCTCTCTGA | 5336 |
| rs536236519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920557 | GGAGAAATGTGAGCC[A/G]AAACATGGAAGATAG | 5336 |
| rs536261761 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877380 | GAATGGCGTGAACCT[-/G]GGAGGCGGAACTTAC | 5336 |
| rs536264849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957630 | CATAATATGTCTAAA[C/T]CTTCTAAGAAAGAAT | 5336 |
| rs536268524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792942 | CAGTTTCCATATCTG[C/T]CAAGTGAGATAATAG | 5336 |
| rs536270529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846127 | TGGGTGTCGTGGCTC[A/C]CAGGTGCCCCTTCTT | 5336 |
| rs536284104 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827275 | CACTGCAGCCTCAGC[A/T]TCCCAGGATCAAGTG | 5336 |
| rs536288773 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81938467 | GTTCCTCAGCCTTTC[C/T]TAGGGGTGTGGAAAT | 5336 |
| rs536290635 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953573 | GGTAAAACTTATTAC[C/T]AAAAGCTTCATTTTC | 5336 |
| rs536305889 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955839 | TGGCTACAGGTGAGG[C/T]ACATGCCCATCTCTG | 5336 |
| rs536324539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871598 | CCGCCTCCACTTCCT[A/G]AAGTGCTGGGATTAC | 5336 |
| rs536339477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878832 | TGTTGGTTCTCTTGC[A/C]GCGTTTGTGGCTCTT | 5336 |
| rs536371224 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941736 | GGAGTCTTGCTCTGT[C/T]GCTCAGGCTGGAGTG | 5336 |
| rs536375881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881940 | TACAGGCATGTGCCA[C/T]TGTGCCCAGCCATAA | 5336 |
| rs536387762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853145 | AGACCAGCCTGGCCA[A/T]CATGATGAAACCCCA | 5336 |
| rs536393167 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961272 | AAATGAAATTGAAAA[C/T]GGAAAATAGAATTGA | 5336 |
| rs536405629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865570 | TCTTGAGCAGCTGCT[C/T]TGGCACCCCAGGCCC | 5336 |
| rs536430297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888128 | ATGACAATGGCAATA[A/G]ATGACTTGCGGAGTT | 5336 |
| rs536437839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917101 | CTACTCTCCACTTCC[A/G]TGAGTTTAAACCTTT | 5336 |
| rs536443058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811924 | GGTATTTCTGGTGCT[A/G]GATCCTCGAGGAATT | 5336 |
| rs536445298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832842 | GGGAGACCCTGTGGG[A/T]GACCCATTAGCCATA | 5336 |
| rs536448281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916836 | AAAGGTGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 5336 |
| rs536466520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842903 | GCTGAGGGAGGGTGG[C/T]TGGAGTGGGGTGCCG | 5336 |
| rs536467414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847096 | TTGACTGACTGGCTA[A/T]AAATTGGGGTTCCAA | 5336 |
| rs536474117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789624 | TCTGTTCAGCCTCTT[C/T]ATTTCCTTCTTCTTT | 5336 |
| rs536483574 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821791 | GCTTTGCATAACTTC[A/C]TACCCAAAAGAAAAG | 5336 |
| rs536488387 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860303 | GTGTTGATGCACAGA[C/G]CGCTGCTCCCAATCC | 5336 |
| rs536491329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869078 | CAATGTCTTGTTCCC[A/G]GTTAGTGGTCCATAA | 5336 |
| rs536504628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846857 | TTTCTCTTTCCTCTT[C/T]CCTCTGTACTCAACA | 5336 |
| rs536535795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897677 | CAGCCTCCCGAGTAG[C/G]TGGGATTATAGGCAT | 5336 |
| rs536536947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789203 | TCATTGTGATGGGCA[C/T]GAGACAGGATTTTGG | 5336 |
| rs536557658 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795168 | AGGATCTTACAATCT[G/T]GTAGGAAAAGCAGAA | 5336 |
| rs536573500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911399 | AACTGTGCCTCCCTG[G/T]GAGCCTGGCTTTTCA | 5336 |
| rs536586294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892606 | AGTTTGTGTTTCAGC[A/G]TGGTGAATTCTAGAA | 5336 |
| rs536623265 | in-del | -/TCCCTCCCTCCCTCCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803634 | CCTTTCTTTTCTTCT[-/TCCCTCCCTCCCTCCC]TCCCTCCCTCCCTCC | 5336 |
| rs536625876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815836 | GAGGCCAAGGTGGGC[A/G]GATCACTTGAGGTCA | 5336 |
| rs536630110 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872052 | ATAGAATACAGGCCA[C/G]GTGCAGTGGTTGACG | 5336 |
| rs536653055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805315 | CCATCCTGACTAACA[C/T]GGTGAAACTCTGTCT | 5336 |
| rs536658050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916317 | AAAACAACGTTTTTT[A/T]AAAAAAGAAAAAAAT | 5336 |
| rs536679055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868758 | CTGGTCATTTGACAT[C/T]ATTTTCTGCCCACAC | 5336 |
| rs536726443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793377 | GAGTTGAGCCTTAGG[A/T]GTCCTCTTGCATCTT | 5336 |
| rs536727452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904055 | GTGGACATTGAGATT[C/T]AGAGGTTAAATAGCT | 5336 |
| rs536732319 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81898383 | TTTGATACCAACTTA[C/T]TAGGTAGCCTTTGTT | 5336 |
| rs536767523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868413 | GGGGTCCCCACTTAC[C/T]CTGCATCCCTCTTGT | 5336 |
| rs536776783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936937 | ATTTAATAAGTCCCC[A/G]TGGAGGCACATGTAG | 5336 |
| rs536783909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948835 | TGAACACACAAAACC[A/G]TGAGCATGCAGTGGA | 5336 |
| rs536785896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797355 | GTTTTTGTATATCAG[C/G]CTCGCAAAATTATGT | 5336 |
| rs536793496 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908253 | GCAGGCAGAGGAGGG[G/T]AGCAGGTGCTGTTTT | 5336 |
| rs536813410 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957679 | AATAGTAGCCACCAA[A/C]GAGAAACTGTGCTGC | 5336 |
| rs536826818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816159 | GAGGATCACTTGAGG[C/T]CAGGAGTTCGAGACC | 5336 |
| rs536852894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805212 | TCTTAAAACTCAACA[A/G]TAAAAGGCCAGGCTC | 5336 |
| rs536855624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921598 | GTGTTTATAAATTCC[A/G]TTTGGTTCACTGACC | 5336 |
| rs536888464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873177 | ACTTGACCTCTAACT[G/T]ACCAAGTAATGTTGG | 5336 |
| rs536896070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820072 | AAGATGTCCTATTTC[A/G]TCTTTAAGGATTATG | 5336 |
| rs536896270 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800551 | GACACGATCTCGTTC[C/T]GTTTTATGGCTGCAT | 5336 |
| rs536896616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812276 | GGATGGTCTTGATCT[C/T]CTGACCTCGTGATCC | 5336 |
| rs536907793 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961411 | ACTATGTTTAATAAT[C/T]TAGTGAAATTTGGGC | 5336 |
| rs536909680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808570 | ATGATCTCGGCTCGC[C/T]ACAACCTCCGCCTCC | 5336 |
| rs536916790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925539 | CACTCTGCTTATTCA[A/G]ACCAAAAAATTGTTA | 5336 |
| rs536930702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786441 | GGCATTCAGGCAGCT[C/G]TCCTTGCCTGGTGGT | 5336 |
| rs536931585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949798 | AAAATGACAATCAAA[A/G]GCTAAAAAATAATCA | 5336 |
| rs536931613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798190 | TTACCCCATCAGATC[A/G]CTGGGAGGATTCAGT | 5336 |
| rs536940772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937035 | AGATGTAGGAATATG[C/T]CTATGGGACAGAATT | 5336 |
| rs536949771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860797 | GCAACACGGTAAAAC[C/T]CTGTCTCTACTAAAA | 5336 |
| rs536964138 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824064 | CTGTCCTGTCCTGTC[A/C]TGTCCTGTCCTGTCC | 5336 |
| rs536977545 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861743 | AGAGAGGGAGCCACC[C/G]TCAGTGCCTCTCTCC | 5336 |
| rs536979505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885183 | AGGCGTCTGCCACAA[C/T]ACCTGTATTTTTGTA | 5336 |
| rs536985808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838813 | TATATATATATGTAA[A/G]TAACATAGATGTGGT | 5336 |
| rs536988017 | in-del | -/AT | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811828 | AGTGCCGCAATAAAC[-/AT]ATGTGTGCATGTGTC | 5336 |
| rs537001619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789648 | CTTCTTTCTCCCTGG[A/G]GAGACCAAGAATGAT | 5336 |
| rs537026969 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898253 | TCTGTAATCAAACAT[A/T]AATGCATTAATGTTT | 5336 |
| rs537036169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846896 | ACCAGATGTGTATGG[A/T]TTTCCCCCCACGCAT | 5336 |
| rs537041231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911989 | TTTTTAGTAGAGACA[C/G]GGTTTCACCGTGTTA | 5336 |
| rs537045542 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824264 | TCAGCCTCCCAAGTA[A/G]CTAGGATTATAGGCA | 5336 |
| rs537049552 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936039 | ACAATATCATCAGAA[-/C]CCCTTGAATGTCAAA | 5336 |
| rs537063295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789275 | ATACCATTTCACTCG[C/T]TTACGCGGATGCGCT | 5336 |
| rs537067458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842457 | CCTAGCGCTCAGCGT[C/G]GGGTTCTGTGACTGC | 5336 |
| rs537068859 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820795 | TGGCTAATTTTTGTA[-/T]TTTTTAGTAGAGGCA | 5336 |
| rs537086384 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811694 | TCCCTGCAAAGGACA[C/T]GAGCTCATCCTTTTT | 5336 |
| rs537101978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892653 | AAGAAATACAAACTT[A/T]AAAAAAAAACTTTTA | 5336 |
| rs537103862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842201 | CCTACAAAGGGAGGC[G/T]TTCTCCTCTTCTTCC | 5336 |
| rs537107138 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784841 | GGTGGTTCAGCTCCA[C/G]GGCCTGGGGAGCGCC | 5336 |
| rs537109213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846477 | AACATGCAAAACATT[A/T]GCACTCTGCCTAACA | 5336 |
| rs537120662 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945677 | ATTGTAAAGAGGGAA[C/T]GGCTTTAGGAGGAGG | 5336 |
| rs537129070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879253 | CTAGCCCCTGATGCC[C/T]TCAGCAGCAGGCTGA | 5336 |
| rs537159782 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922821 | TTTATGCCCGCCAGG[C/T]AGAAAGCATGAAAGC | 5336 |
| rs537167933 | in-del | -/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962551 | TTAAAGCTTAATTTA[-/T]TTTTTATATAAATAG | 5336 |
| rs537173949 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958164 | GCATGAGTTGGGGTA[A/C]TTTCCTATTATTTTC | 5336 |
| rs537174123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953682 | TCTTGACTAGAGTGG[C/T]GGTTCCTCAAGTCAA | 5336 |
| rs537177808 | in-del | -/CA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907036 | AGACAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 5336 |
| rs537190554 | in-del | -/TTT | 0.167809 | 0.236103 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818884 | GTGTGGGCTCATGGA[-/TTT]TTTTTTTTTTTTTTT | 5336 |
| rs537192957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901062 | GCAGAATGCGTGCAA[C/G]TGCGCCTGTCATGTG | 5336 |
| rs537202840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791050 | CTGAACCCTGTTTGG[A/G]TGGAATTTTCTCATT | 5336 |
| rs537204469 | snp | A/G | 4.96874e-05 | 0.0049841 | missense | PLCG2 | GRCh38.p7 | 16:81786090 | CTGTGTTCAGCTTCC[A/G]CAAGTCCACCCCCGA | 5336 |
| rs537216249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781733 | GTATTTGCCTGTGCT[C/G]CATTTTAACACAATT | 5336 |
| rs537219154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901782 | GGAATTATGGAGGTT[A/G]TTAGGTCTGCCTCTA | 5336 |
| rs537237488 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961678 | GATCATAAAAAAATG[G/T]CCCTGTTCATAAAAT | 5336 |
| rs537239761 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861735 | CAGGGCTGAGAGAGG[A/G]AGCCACCCTCAGTGC | 5336 |
| rs537239807 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81905033 | GCTGGGATTACAGGC[A/G]CGTGCCACCATGCCC | 5336 |
| rs537257093 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907314 | TCGGGGGAAAAAAAA[-/AAG]AAGTCATTAAGCCAC | 5336 |
| rs537260897 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874045 | TGGCAAAGATTCTGC[C/T]GATACCAAAGGTTGA | 5336 |
| rs537264752 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908284 | CCCATACCCCTTCGG[G/T]TGGGGACCAGCTGAG | 5336 |
| rs537269253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885908 | GATGATCAAAAGAAG[A/G]CTTATTTGCCCAACC | 5336 |
| rs537270443 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860522 | GCACCCTTTCCTGAT[G/T]ATTTATTGTGCCATT | 5336 |
| rs537272832 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785764 | CTTCAGTTTCCATTT[A/C]AACCTTTGTGTCCTG | 5336 |
| rs537279754 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814681 | GCCTGGGCAACAGTA[C/T]GAGACTCTGTCTCAA | 5336 |
| rs537297766 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959770 | TAGCCTTTGGCCAGG[C/T]AGCCACCAGAACCTA | 5336 |
| rs537304017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889388 | GCTGTATGATGTTGC[C/G]TCGACTGACTGGTTA | 5336 |
| rs537315351 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883635 | GCAGGAGGGGTGAGG[C/G]CCTGAGGATGGGGCT | 5336 |
| rs537319114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917155 | GTGGTATTTGTTTTT[C/T]TGTGCCTGGTTTATT | 5336 |
| rs537320232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839251 | ATCAGCAGTAGGCAG[A/T]TACAACAAACCTTAT | 5336 |
| rs537366945 | snp | A/C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945465 | GTTCCTTTTAGGACA[A/C/G]AGAGGAGGATTGGGT | 5336 |
| rs537377413 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912412 | CTGGGGTCTTCCACT[A/T]TTCTTTTCACAAATT | 5336 |
| rs537395101 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888851 | TAAACAAAATATTGT[C/T]GGAATACAACCATGC | 5336 |
| rs537405832 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876549 | TCCAGCTGGTAACTT[C/T]TCCTGGGGCCCGACT | 5336 |
| rs537411285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873258 | TTAAATGAGATCAAT[A/G]GTTATAAAACTTTTA | 5336 |
| rs537430262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852316 | CCGAACCAGTCACTG[A/G]GCCAGGGCACTTGGG | 5336 |
| rs537445486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802225 | TCACACCATTCTCTT[G/T]CCTCAGCCTCCACAG | 5336 |
| rs537473714 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852536 | TCACTGGTCATCTTG[C/T]AGGGGGAAGGAGGAG | 5336 |
| rs537476603 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946852 | AACTGTAAAACCTGG[C/G]CTTTAGCAGAAGCCT | 5336 |
| rs537504709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928971 | CTGGCTGAAATGCAG[C/T]GTGGAGTTGGGAGTC | 5336 |
| rs537527411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899121 | TTGAACTTGGGAGGC[A/G]GAGGTTGCAATGAGC | 5336 |
| rs537528311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880368 | AATGTGCTGTGTCTA[C/T]GCGCTTTTCCTTCTA | 5336 |
| rs537541853 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932482 | TCCCATGCACCCATT[G/T]GTTTCTAAGGTAGAA | 5336 |
| rs537550896 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916352 | ATTTTAAAACAAAAA[G/T]TCTCTCTATAGTGCA | 5336 |
| rs537557316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935121 | TATTCTTGCACAGTC[C/T]TGGAGGCCAGAGTCT | 5336 |
| rs537577977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955684 | GTGGCCATGACAGGA[C/T]CACACTTACTCTTTC | 5336 |
| rs537582680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853797 | TGGAGGCTGTGGCCC[A/G]TTAGTAACAGTCCAT | 5336 |
| rs537587932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805355 | ATATAAAAAATTAGC[C/T]GGGTGTGGTGTCGGG | 5336 |
| rs537593826 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904455 | TGTCTTAATCTTGCA[A/C/G]ATGAGAAGCCTGAGG | 5336 |
| rs537634363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915148 | ATGAGTGCTACAAAG[C/G]GATTGGTCAGGCAGG | 5336 |
| rs537642709 | snp | G/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779239 | GGGGCGAGGCTGGGC[G/T]GTGCGGGGGGCGGCC | 5336 |
| rs537660239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914801 | TGGTTGGTGAATGCT[G/T]GCTCAGTGAATCAAT | 5336 |
| rs537662923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792429 | GAGGCTGCAGTGAGC[C/T]GAGATCACTCCACTG | 5336 |
| rs537663452 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81786654 | AGTGAGTTGTTGAAC[A/G]TTTTGTAGCTTTCAA | 5336 |
| rs537663495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917643 | GATGATTAGTGATGC[C/T]GAACATTTTTTACGT | 5336 |
| rs537671987 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865864 | TGAGCTCCAACTGGG[A/G]CACCAGCATGAGAGG | 5336 |
| rs537672438 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841348 | CTCAAGCCGTTCTTC[G/T]CAGCCTCCTGAGTAG | 5336 |
| rs537682124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816557 | ATCACAGCTCAACTA[C/T]TGCCTTGACCTCCTG | 5336 |
| rs537707713 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895759 | GGCTGACCTCGGGGC[C/T]GTCAGTGAACACACG | 5336 |
| rs537719678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941797 | TGCCTCAGCCTCCTC[A/T]GTAGCTGGGACTACA | 5336 |
| rs537727178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946022 | TAACCATCAGGATAG[G/T]ACCTCTGGCTTCCAC | 5336 |
| rs537729106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794662 | AAGACTCTTGTGATA[A/G]GTAAATGACGTGATA | 5336 |
| rs537760176 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803219 | TGCCTCATGGGTTCA[C/T]GCCATTCTCCTGCCT | 5336 |
| rs537762898 | snp | A/G | | | splice-acceptor-variant | PLCG2 | GRCh38.p7 | 16:81905401 | ATATGTTTTCCCCTC[A/G]GCATAAGAAGCTGGG | 5336 |
| rs537781168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798639 | TGGAGGCCAGGGGTA[C/G]GCGTGAGTTTTGGGA | 5336 |
| rs537793524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952156 | ACATAAAATCTTATT[A/T]AAAAACAAAACACCA | 5336 |
| rs537794446 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877904 | TGTGCCAGTCTCTGC[C/G]TCCATCATCACATGG | 5336 |
| rs537794450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895508 | GAGATTGCAATGGGC[C/T]GAGATTGTGCCACTG | 5336 |
| rs537800663 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951635 | CTTTCCCCTAACCTC[A/G/T]TTCAGCCGTAGACCA | 5336 |
| rs537802267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907173 | AAACGTTATTAAAAA[A/G]AAGAGTTTCTGCATA | 5336 |
| rs537816222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780276 | CTTTTTGAGTCTGTT[A/T]CCCCCTCTGGATACT | 5336 |
| rs537838787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807805 | GGTGGAAGGTGAAGG[C/T]GGGGCTGGCATGTGA | 5336 |
| rs537846196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856213 | TGTGGGAAGATGAGA[A/G]CAGCAGTCTCTGCCA | 5336 |
| rs537875192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784475 | GCTGGAAGCACAGAC[A/G]GCCCTGGCTGAACAC | 5336 |
| rs537876422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825785 | ACTGAGCCCCTCCAC[A/G]TGCTGGAGACTCTGC | 5336 |
| rs537877863 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952972 | GTTACCAACCACCTG[A/G]AATAAGGCAGGTTGA | 5336 |
| rs537882961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859872 | GTAGAGATGTGTTGG[G/T]TGATGTGATAACGTA | 5336 |
| rs537904436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803313 | TTTTAGTAGAGATGG[A/G]GTTTTGCTGTGTTAG | 5336 |
| rs537919574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852014 | GATGCCTTTGCTCAC[C/T]TCTGGACTTCGTTCT | 5336 |
| rs537947369 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855458 | GGTGAGGCAGCTGTC[A/T]AAGTTGAGCAATATA | 5336 |
| rs537951518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935623 | ACCTTCAGGGACTCA[A/G]CAGGCTCAGCATGTT | 5336 |
| rs537953549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930398 | GCTCATGGCTGCATT[C/T]TTCAGTCTCCACATT | 5336 |
| rs537959535 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793506 | TGAGGGCCTGGATGC[A/G]TCCATCTCAACTGTG | 5336 |
| rs537962004 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777907 | CTATAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 5336 |
| rs537983071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841572 | GCAAAGTTTTTTTTC[A/G]GATATATCTCTATAG | 5336 |
| rs537986349 | in-del | -/GCT | 0.0279526 | 0.114869 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834592 | CCCTGGATCTGCAGA[-/GCT]GCTGCTGCTGCTGCT | 5336 |
| rs538006533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943727 | GTCTGCAAGAATTCT[C/G]AGTCTCTATCAAGGC | 5336 |
| rs538035486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924701 | TGCAAACCAATTCAT[A/T]CCTAGATTCCACAGA | 5336 |
| rs538037820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863645 | TTATTTTGCCGGATT[A/G]CTATACTGTTTTCTG | 5336 |
| rs538058674 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856313 | TGTTAGCTTCATTTT[A/G]CAGGTGAGATGAGGC | 5336 |
| rs538064964 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887524 | TCCCACCTTCCTAGC[G/T]GTTTTGGGCCCCTGA | 5336 |
| rs538077714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818195 | CGGCCCTCTGTGCCT[C/T]AGTTTCCTCACTGGT | 5336 |
| rs538097275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924415 | ACGTTTGAAATAACT[C/G]ACTTCATTTGAAATA | 5336 |
| rs538100900 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952710 | AAGAGATAGCTCTTC[C/T]TTACAAATGAATTCT | 5336 |
| rs538102193 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923697 | ACCCCCTTTGTCATC[C/G/T]TGGGCTGGCTTTGAC | 5336 |
| rs538102756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875378 | AGAGGTTACTTTGCT[G/T]AAGGCCTGTTTACTG | 5336 |
| rs538115446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800738 | AACGCTCTCTGCTCC[C/T]AAGATGCCCTTGTCT | 5336 |
| rs538157943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871199 | CCATAAGTTTGATTG[G/T]AATTTGATCTGAGTC | 5336 |
| rs538170950 | snp | A/C | 1.65655e-05 | 0.00287793 | missense | PLCG2 | GRCh38.p7 | 16:81931601 | GACAGGGTGGAGGAG[A/C]TCTTTGAGTGGTTTC | 5336 |
| rs538173357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804340 | TGTAATAATTTCCTT[C/G]TAAACATTGGCTTTC | 5336 |
| rs538178058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947457 | TCGCTCTTGGAAGCC[C/G]AGCTGAATTGCATTC | 5336 |
| rs538180626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800124 | GGATTAGGGGAGTTA[A/C]TTATGTATCATACTT | 5336 |
| rs538182257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796013 | TAATTTTGGAGGGTA[C/G]AGAGGCAGCTCTAGG | 5336 |
| rs538186756 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844406 | CTGCAACCTCTGCAC[A/C]CCCACAATGGGTTCA | 5336 |
| rs538191658 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867945 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 5336 |
| rs538192415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834355 | GCAGAATTGTGAGGG[C/T]GGTCTGTGTGAGAGT | 5336 |
| rs538199180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903351 | GAAACACCAAACAGT[A/G]CAAGGAGCTTTGGCC | 5336 |
| rs538208486 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906229 | CAGGATCCAGTACCC[A/G]GTGCTGCCGTGCATT | 5336 |
| rs538211955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881257 | AATAGTTTTTTTTTT[A/T]AATTACAAAAACTAA | 5336 |
| rs538220323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947959 | ATTCATACAGGTGCC[C/T]TTTTCTACTTCACAG | 5336 |
| rs538265497 | in-del | -/GAG | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833013 | CTTGTGAGATGTGAT[-/GAG]GACCTGGAAAGGGAA | 5336 |
| rs538273664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826497 | ATAAAATCGCAATAA[C/T]AGTAGGACCTATCTC | 5336 |
| rs538298147 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870026 | CAAAAAGCTCATTTC[A/G]TTTTTGTATTAATGA | 5336 |
| rs538313030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927479 | TTGTCCTTTGCTTAA[A/G]CAACTTGCAGATGAA | 5336 |
| rs538319527 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891703 | AGCAGGTGGAGGGTG[C/T]AGCACCGCATTCCTT | 5336 |
| rs538327498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935705 | CCCCTTCCCTCTCCT[C/T]CTGTTCTCCCTTCCC | 5336 |
| rs538336811 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826273 | GAGATGTGCTTCCCT[C/T]TGCCACGGCAAGGCT | 5336 |
| rs538339321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899712 | CTGGTGTTCCTGAGC[A/G]GGAGAAGGCTGTGAT | 5336 |
| rs538342465 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884206 | AAATACAAAAATTAG[C/G/T]CAGGCATTGTGGTGG | 5336 |
| rs538342596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939705 | AGCCTGCAACAGCAG[A/C]TTCCAGGATTGCTCA | 5336 |
| rs538365203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815021 | GCTTGTTCCAGTGGC[C/T]GTTCCAGCCTGACAA | 5336 |
| rs538372375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931203 | AATCCAGGATAATCT[C/T]ATATTGAGATCCTTA | 5336 |
| rs538383962 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828541 | CCGCACCCGGCCGAG[A/G]AGCGTCATTTTTATT | 5336 |
| rs538388869 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948492 | TAACCTGCAAGGGGT[A/C/G]GAGAGGCCCTTCTTT | 5336 |
| rs538392988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875588 | GTCACTGCCCTCACC[C/G]AAGTCCCTTTTCTCA | 5336 |
| rs538402602 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900495 | AGATGTGGGGGTTGT[C/G]CCCCCCGAGCAGCGC | 5336 |
| rs538419029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856779 | GAAAAGGAGACTTGG[C/T]GGGTGTGGTTAAATT | 5336 |
| rs538424307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896447 | TCTGGGTGTAGTGGC[A/G]TGTGCCTGTAGTCCC | 5336 |
| rs538438886 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822984 | CACCTTGGTTTTAGC[C/T]CAGTGAGACTGGTTT | 5336 |
| rs538455081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957204 | CTTGGGAGGCTGAGG[A/C]AGGAGAATCATTTCA | 5336 |
| rs538471238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826931 | GGAGATCCGCAGAAC[C/T]AGCCTCCTGCCTCCT | 5336 |
| rs538498684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815042 | AGCCTGACAAATCTT[C/T]CAAGGCAAAACCAGA | 5336 |
| rs538530562 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881564 | TGATCCAGTCTTTAT[C/G/T]GGTGAGCAACTTTTC | 5336 |
| rs538531333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830240 | TGGGAAGATCACCTA[A/G]GCCCAGGAGGTTGAG | 5336 |
| rs538534648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841614 | TTTTTCCATTTCATA[A/G]ATGAGAAAATAGACA | 5336 |
| rs538555654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948267 | ATATCCCATCTTGCC[A/T]TTAACTGGAATAGGC | 5336 |
| rs538556174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807920 | ATTGCAAGGACAGCA[C/G]CAAGAGATGGTGCAA | 5336 |
| rs538559422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940168 | TGGTTTGGATGGAAT[C/G]ACTGTAAAACCGATT | 5336 |
| rs538562736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818624 | GCCTGAACAATAGCC[A/G]GGACAGAGCCAACTA | 5336 |
| rs538565176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956971 | TTCTGGAAAGCCCTC[G/T]GAGTTGCTTTCTTCA | 5336 |
| rs538580921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845736 | GGGATCATCATTCAC[C/T]AAGATGCCCCTGCCT | 5336 |
| rs538594609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818252 | GTGGCTCAGTCAGCT[C/T]CTCACTTCCTGCCCC | 5336 |
| rs538600912 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782384 | AAGGGATTTCAAGGC[-/T]TTTTTTTTTCTTTTT | 5336 |
| rs538627901 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853222 | TGTAATCCCAGCTAC[G/T]CCTGAGGCTCAGGCA | 5336 |
| rs538643635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845312 | CAGAGAAGCTTCTAC[A/G]TCTTTGTTTTTTTTC | 5336 |
| rs538652570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804720 | ACCGTTTTCCCAGAG[C/T]CCTGGAAATGCTTCT | 5336 |
| rs538659046 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960823 | CTGGGAGTATACCAG[A/G]GCTTTCCAAGGAATA | 5336 |
| rs538670706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903373 | GCTTTGGCCAAGCAC[A/C]ACCAGAGGAGGGGAT | 5336 |
| rs538689301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852607 | GTTTTGACCAGGAGT[A/G]GATGGAGTCACATGG | 5336 |
| rs538693063 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830407 | CACTTCTTGGGTTCA[A/C/G]GCGTTTCTTGTGCCT | 5336 |
| rs538693765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923383 | CTTGGCCTGAAGCCT[C/T]CTGCTCCCCAATGAG | 5336 |
| rs538711615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800203 | CTATTGCTATTATTA[C/T]TGTTTAAATTTACTT | 5336 |
| rs538720387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856666 | ACAAAAAGCTAAATC[C/G]CTAAGCCAGTGGTAC | 5336 |
| rs538741779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780310 | GCCACCCAATTTTCC[A/T]GGGCTGTGTCGAGAA | 5336 |
| rs538746540 | snp | C/T | 3.31318e-05 | 0.00406999 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81927097 | GTGGAAAGGAGACTA[C/T]GGAACCAGGATCCAG | 5336 |
| rs538785976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902974 | GCCCCCATGATTCAA[C/T]TACCTCCCACTGGGT | 5336 |
| rs538789954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834087 | CCACTGTGGGCCACC[C/T]GCACAGACTACCCTG | 5336 |
| rs538800234 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794740 | ATTTTTTGCTCTTGC[A/T]GTCGTTGATGTCATC | 5336 |
| rs538808567 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865652 | TGGGCTCCTGGGGGG[-/A]CCCTGGCCTCTTCCT | 5336 |
| rs538823853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819616 | TTGAGACCAAGCTTC[A/G]CTCTTTCGCCCAGGC | 5336 |
| rs538825553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864639 | ATATGTGAAGGGTGC[C/G]TGGACCTGCCTGGCT | 5336 |
| rs538830448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921040 | CTTCTTTATAGCTTC[C/T]TCCTGTGTCTACTCA | 5336 |
| rs538830770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916425 | GTTAAATGAGCAGTA[C/T]GCCCATAGAAACGAT | 5336 |
| rs538834011 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881111 | TCCCATGCCTGTGGC[A/C/G]TGGATAGAGATGAGC | 5336 |
| rs538839026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911092 | TAAGAGTCTCCCGCT[A/G]ATTTTTTTTATCTAG | 5336 |
| rs538842103 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953746 | TAAACTGTTTCTATC[-/T]TTTACGTTCTTTTCT | 5336 |
| rs538843407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884247 | TCCCAGCTACCTGGG[A/G]GGCTGAGGCAGGAGA | 5336 |
| rs538853486 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932796 | TCCTGGGGGCCTTCC[C/T]TAGGGCTCCTAATTC | 5336 |
| rs538860448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797774 | TGGTCCTGGCACTTA[C/G]TGACTGTGTGACCTT | 5336 |
| rs538877456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837779 | TAAAGATGTAAGAAA[C/T]GATACAGAGAGATCT | 5336 |
| rs538879320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887944 | CATGTATATTTCAGA[C/T]GTTATCAGTGTTTCA | 5336 |
| rs538882843 | in-del | -/TTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818905 | TTTTTTTTTTTTTTT[-/TTT]ACTGTGGTGGGGCTC | 5336 |
| rs538915081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797406 | AGATTTAGGTGCTGT[A/G]CAGTTTGGGGTTGAA | 5336 |
| rs538920565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924801 | GCTGACATTGCTGTT[C/G]CTACTGCAGCCTCTG | 5336 |
| rs538928863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896843 | ATCCCCATTTAACAG[A/G]TGAGTAAATTGAGAC | 5336 |
| rs538935289 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782382 | AAAAGGGATTTCAAG[G/T]CTTTTTTTTTTCTTT | 5336 |
| rs538949445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867959 | CCGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 5336 |
| rs538954463 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915356 | CCAGTAGAGGAGAAA[C/T]ACCTGCTTTCAAATC | 5336 |
| rs538968964 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792464 | CCAGCCTGGGTGACA[A/G]AGCAAGGCTCTGTCT | 5336 |
| rs538982465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796901 | TCATGAGTGGCAGGC[C/T]TAACACACAAATACA | 5336 |
| rs538984789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853516 | ACTGTTCTACTTCAG[A/G]TCATCAGGCATTAGA | 5336 |
| rs538996057 | in-del | -/CTC | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935250 | GCATTCCTTGGCCTT[-/CTC]CTCTTCTGCTTCCCT | 5336 |
| rs538996226 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801151 | ATGCATGTGGGAATT[A/C]AGTAGCGTAGCGATT | 5336 |
| rs539005465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905140 | GATCTGTCTGCTTCA[C/G]CCTCCCAAAGTGCTG | 5336 |
| rs539006978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878799 | ATGCCCGACTGTCTT[A/C]CTTATCTTGCCTCTC | 5336 |
| rs539016518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832465 | CATGATCACGGCTCA[C/T]TGCAACCTCTGTCTC | 5336 |
| rs539023250 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906858 | TCCTGGCTAACATGG[C/T]GAATCCCCGTCTCTA | 5336 |
| rs539026331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881821 | ATTGTTTTTTTTTTT[G/T]TTGTATTTTTGGTAG | 5336 |
| rs539031379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808458 | GTTTGAGTCTCAGCT[C/T]TGCCACCTACCACTG | 5336 |
| rs539044813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956998 | TTCAGAAATCCTTGG[C/T]CGGGCATGGTGGCTC | 5336 |
| rs539047553 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858432 | CCAACATGGGCTACA[-/G]GGGGGGAAAAAAAAA | 5336 |
| rs539054725 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957373 | GTTCTAGAAATTAAC[A/C]TACAGTAATACCTTA | 5336 |
| rs539066713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909609 | TTTTGTAGAGCTGGA[C/G]TCTCACTACGTTGCC | 5336 |
| rs539068494 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904816 | TGTGTGTAGGGCTAG[A/T]CAAGTGAGAGGAATA | 5336 |
| rs539074651 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81783473 | CTCTTTTGAGAGTGG[C/T]AAGTACTGGCAAATC | 5336 |
| rs539090384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929339 | GGACTCAGGTGACAG[C/G]AGCCCCAGGAACTTC | 5336 |
| rs539095046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807983 | AGTCACCTTCCACCA[C/G]ACCCCACCTCCAGTA | 5336 |
| rs539108021 | in-del | -/T | 0.0718919 | 0.175435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812043 | CTGTTGTTTCCTGAC[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs539151930 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811481 | TCCGTTTTCTTTTTT[C/T]TTTTTTTAGGTATTT | 5336 |
| rs539163932 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960397 | GAAGCAGCACTGATA[C/G]ATCAAAACCACCACT | 5336 |
| rs539185886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840184 | AACATCGGCAATCAA[C/T]GAAGGGCGATGAGAT | 5336 |
| rs539197347 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962057 | CCCTCCCGAAGCTGC[A/G]CGCTCCGTCGAAGAG | 5336 |
| rs539218604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874352 | GCTTTGGCAACCCTC[A/G]TCTCCACTGTTTGAG | 5336 |
| rs539227875 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898994 | GTTTGAGACCAGCAG[A/C]CTGGCCAACATGGTG | 5336 |
| rs539229131 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946633 | GGAATCCTATCAAAA[A/G]GTCTGATAGCCTCCA | 5336 |
| rs539234773 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961838 | ATAATGAGAAATTTT[A/C]GATGTCAATATAGCA | 5336 |
| rs539234860 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803279 | GCCCACCACCACGCC[C/T]GTCTAATTTTTTTTG | 5336 |
| rs539239273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918236 | CTTTCACTTTTGTTG[C/T]CTGTGCTTTTGGGGT | 5336 |
| rs539259452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799486 | TTGGTGTGCAGTGGT[A/G]TGACCATAGGTCACT | 5336 |
| rs539264450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925099 | TCTGTGTGAGATGGC[C/T]TCATGCCTTTCTATG | 5336 |
| rs539264804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823654 | CCTCAGTCTCTCAAG[C/T]AGCTGAGACTACAGA | 5336 |
| rs539278641 | snp | A/C | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962602 | AGAATTAAGTGAATG[A/C]GTCACACAGATGTTG | 5336 |
| rs539294682 | in-del | -/GTTTTG/TTTTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825299 | TTTTTTTTTTTTTTT[-/GTTTTG/TTTTG]TTTTTTTGAGACAGA | 5336 |
| rs539299362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851605 | GCAACCTCCGCCTCC[C/G]GAGTTCAGGCGATTC | 5336 |
| rs539321605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798931 | ACCAGCCACTCCAGG[A/G]TGTCCCTGGCCTGCC | 5336 |
| rs539325122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953592 | AGCTTCATTTTCTAA[C/T]AAAACAAACTAAATT | 5336 |
| rs539326329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802869 | TTTATTGAGATAAAA[A/T]CATTGTATACCCTAT | 5336 |
| rs539328642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898562 | TATTTTCACATTTGC[C/T]TTCATTTCTATTGAG | 5336 |
| rs539329412 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827249 | TGGAGTGCAGTGGTG[A/C]CACTATCGCTCACTG | 5336 |
| rs539345622 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946986 | TTGCCCGGGGAAAGG[A/G]AACCAGTGCTGCTTC | 5336 |
| rs539350561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823391 | CAGTCCCTGAAATGC[C/T]GCTCCCCACCCCTCG | 5336 |
| rs539351447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805045 | TTGCCCAAGGTTACC[A/C]AAGTTTTCAGAGGAA | 5336 |
| rs539355765 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932627 | TTTTTCCCCTTGGGA[C/G]GGCCTCACATCTTGG | 5336 |
| rs539367678 | in-del | -/CC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803644 | CTTCTTCCCTCCCTC[-/CC]TCCCTCCCTCCCTCC | 5336 |
| rs539380046 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959036 | TGTGCGGCTGGCCAG[G/T]GCTTTACACCTCTGC | 5336 |
| rs539382875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802566 | AGATTTGTTTTCTTT[C/G]TTTTTTTGTTTTTGT | 5336 |
| rs539387272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851436 | TGTCACGTGTAGGTG[A/G]GTATGTCTACCACCG | 5336 |
| rs539388644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806435 | GGTGTGACATCTGAT[G/T]GCTGGGCCCGAGCAT | 5336 |
| rs539389219 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854993 | GGCGGGCAGATCACT[G/T]GAGGTCAGGAGTTTG | 5336 |
| rs539389353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953193 | TAGGAGACTAAGGCA[G/T]CACAATGACTAAAGG | 5336 |
| rs539390629 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852701 | ACTATCCCAGTGTTT[A/C]GTGGCTTAAGACAAC | 5336 |
| rs539392152 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884875 | CAGATTAAAAATTAC[A/G]AGCATTTTGCAATTT | 5336 |
| rs539395736 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81817762 | AGAGAGCTGGGGTTA[C/T]AGGCATAAGCCCCTG | 5336 |
| rs539405150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787570 | TAGATTGATTGAGAC[A/C]TAATTCACATAGTAT | 5336 |
| rs539417203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943284 | CTGCAGGCTGTACAG[C/G]CTTTTGTTTCTGGGG | 5336 |
| rs539420276 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962237 | TAAAAAGGACCTCAA[C/G]CCTTTTGACTTTAAA | 5336 |
| rs539425774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814104 | AGGAGAGAGGATAAG[C/G]GGCTGGGAACCCAGG | 5336 |
| rs539434864 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826756 | GGGAAACTGAGTTTC[A/G]TAAAGTAGCAAGAAC | 5336 |
| rs539437163 | in-del | -/GGTAG | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943323 | GAAATTTACAATCCT[-/GGTAG]GGTAGAAGGGGAACA | 5336 |
| rs539447034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933967 | GAGCCCTGATGGGCA[A/G]TCAGAGCTGGGGAGC | 5336 |
| rs539447446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883138 | TTCCTGTTGGCCAAC[A/C]TGGTACCTAACACAG | 5336 |
| rs539469489 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813170 | GGTCTCTTTTTTGGT[A/T]CCATATGAAATTTAA | 5336 |
| rs539475090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867246 | GGTACAGGGAAACTA[A/G]GTGGTTTTCTCCTGC | 5336 |
| rs539488170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858180 | GCTTCTCCCATCTTC[A/G]TGATCTGTATGGGGC | 5336 |
| rs539489170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813686 | GCCTGGAGTCCCTTA[C/T]CTGAATATATTCATT | 5336 |
| rs539490905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817865 | GCAAAAATGAGACAA[A/G]CTCCCTGTGCTTATG | 5336 |
| rs539496219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836081 | AGTTCAACCCCCAAC[A/G]TTACCCGTTTATACT | 5336 |
| rs539522375 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801883 | ACGGGGTTTCACTAT[G/T]TTGGTCAGGCTGGTC | 5336 |
| rs539522653 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862116 | GAGCAACTGACTTCT[C/G]TCCTGCCAATTTCCC | 5336 |
| rs539530960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795917 | CCAAGTGCAAGGGAT[A/G]CTGGGAAACATGCCC | 5336 |
| rs539532892 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938309 | CTTTCAGAGAAAGTG[G/T]TGTTGCTTTGTAAGA | 5336 |
| rs539539023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844641 | CCTTCACTGTTTTCA[C/T]TGGCACCTAGGTGCT | 5336 |
| rs539554050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886196 | ACCCCACCTAGTGGT[G/T]GTTGACTTTATTACG | 5336 |
| rs539556462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821868 | CTCAGACAGATCCAA[A/G]ATGTTTTTTTTTTTT | 5336 |
| rs539576401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848335 | TGATGAAGGCAGATG[C/G]CTGCAGCTCTTTCCT | 5336 |
| rs539586491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821474 | CCTCGAGGGCTCGAA[C/T]GCTGTGTGTCTTGGT | 5336 |
| rs539598152 | snp | A/T | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81889216 | CCGTGAGCGGATGAC[A/T]AAGTTCATTGATGAC | 5336 |
| rs539599485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829378 | CCTCCCAAAGTGCTG[G/T]GATTACAGGCGTGAG | 5336 |
| rs539603369 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956080 | CCATCCCCCAGACCC[C/T]GGTGACCTTTAACCT | 5336 |
| rs539604093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875120 | AGGCATGCACCATCA[C/T]GCCTGGCTAATTTTT | 5336 |
| rs539604407 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862252 | GGCCCAGCCCGGGCA[A/G]TGGACAAGTCTTAGG | 5336 |
| rs539616661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951115 | GAGTAGCTGGGACTA[C/T]AGGCATATGCCACCA | 5336 |
| rs539617277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877716 | TGCTCTTTGGTGTGC[A/C]GACACCATCACTCCT | 5336 |
| rs539624636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894484 | TGGGCAGATGGCAGA[C/T]GCCTTATTTCCCTCC | 5336 |
| rs539633393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815869 | AGTTCGAGACCAGCC[C/T]GGCCAACATTGTGAA | 5336 |
| rs539642004 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807339 | TCTCTGCGAGGAGGG[C/G]ACTGAGGAGGATGGG | 5336 |
| rs539659317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833469 | GCCTCTCCTGTTAAT[C/T]ACTGACAAGGTAAAA | 5336 |
| rs539659332 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876789 | TCCCTTGGTTAGGTA[G/T]AATCTGACCACATAA | 5336 |
| rs539668435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874084 | GGCCAGAATGCCACA[C/T]TGAGCCTGCCCCTGG | 5336 |
| rs539674370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825217 | CCTCAGTGATGCTTA[C/T]TTGGGAGTGTGTTTT | 5336 |
| rs539697597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810849 | TTAGTGGGAGAGGCA[A/C]GCACAACATTGATCA | 5336 |
| rs539724973 | in-del | -/ATAGTCATCATCTTCC | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948349 | AATAGGAAAGCTTAA[-/ATAGTCATCATCTTCC]ATAGTCATCATCTTC | 5336 |
| rs539730013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950812 | TTTAGAAGAGGAAAG[G/T]GCTTGCCTTAAAACT | 5336 |
| rs539731793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955529 | TTTTTTCTCCCCTAG[C/T]GTAATGGACTATTTT | 5336 |
| rs539732104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828798 | CTGGTGAAGTCGGGT[A/G]CATAGAAGGTTTCAA | 5336 |
| rs539736703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935153 | AAATCAGTATCATGA[C/G]GTCAACATCAGGGTG | 5336 |
| rs539737122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929644 | CAAGTGATCTGCCTG[A/C]CTTAGCCTCCCAAAG | 5336 |
| rs539741495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883825 | GGGACAGTCTCCCTG[G/T]ACAGGGTTTGCCTGT | 5336 |
| rs539748854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939202 | AACAGCCCAATCTGA[C/T]TAATCTCCTGAGTCA | 5336 |
| rs539748870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934828 | CTCACAATTATGGCA[A/G]CAGAGGAGAGAGAAT | 5336 |
| rs539765549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902110 | CAAGTCAGCTGTCCC[A/G]TCCTTTTCTCTACTG | 5336 |
| rs539778042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887348 | ATGGTCTCGATCTCC[A/T]GACCTCATGATCCGC | 5336 |
| rs539787742 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934239 | TGGAAACAGCTTTGT[C/T]GAGAATTTTCACAGT | 5336 |
| rs539810559 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81779985 | TGTCTGTGCGTGTTG[G/T]GTTTTGTTGTGTTTT | 5336 |
| rs539813073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863091 | GTTCTTAGATATGTA[C/T]TTCTGTGGGATGAAG | 5336 |
| rs539818708 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917886 | GCCACTGCGCCCAGC[A/T]AATTTTTTGTATTTT | 5336 |
| rs539825462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847535 | AGCCCTACAAAAAGA[C/T]ACTTATCACTGCAGA | 5336 |
| rs539830402 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844107 | TCAGCCTCCCGAGTA[C/G]CTGGGACTACAGGTG | 5336 |
| rs539841466 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887054 | TGATAAATGCAAAAA[C/G]TTTGTAGGGGGAAGG | 5336 |
| rs539842303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840844 | GCAGGGCACGTGGTC[C/T]CTTGGGGGTGGATCC | 5336 |
| rs539845684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794992 | GGAATTGCTTGTCTT[A/G]TTTTCAAGAGTTGTC | 5336 |
| rs539851154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799004 | GCATGACTGAAGGAG[A/G]GCCCGTGTCCCTGGG | 5336 |
| rs539868234 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918412 | CTAGTTTTCTTCTTT[C/T]GAAATTGCTATTATT | 5336 |
| rs539904366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791557 | GGAAGACTGAGCTTA[C/G]CTGGGATTATTTTTT | 5336 |
| rs539909468 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81779307 | GAAGTAGCGAGCGCC[G/T]GCGGCGGAGGGCGTG | 5336 |
| rs539910795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847332 | TAAGCCCTGTCATCC[C/T]GGGTTTTTATGAGAG | 5336 |
| rs539929035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840602 | AGTGTACAACCTGGG[A/T]CCCTCACATGTGCAG | 5336 |
| rs539931816 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947024 | ACATAAAACCCCTCC[A/G]CAGACACTTCACAGA | 5336 |
| rs539943698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873498 | TGTCATCTTATGCAA[C/T]TGACCAGGATTGAGA | 5336 |
| rs539945759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828463 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 5336 |
| rs539948271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844282 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGGCACCTT | 5336 |
| rs539967873 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925724 | AAAACCCTGTCTCTA[A/C]TAAAAATACAAAAAT | 5336 |
| rs539979126 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81903347 | CAGAGAAACACCAAA[C/G]AGTGCAAGGAGCTTT | 5336 |
| rs539998911 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862840 | TTGTGCCACTGAGCT[A/C]CAGCCTGGGCAACAG | 5336 |
| rs540011835 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81904845 | TAAAGCAGGCTTGGG[A/G]CTAGAGAGTGGCAGG | 5336 |
| rs540018291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855806 | AGGGAAAGGCTGTGG[C/T]GTGTGCCAGGGCTTG | 5336 |
| rs540025879 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959731 | GGGATGAGTGCTGCA[C/G]GCACTCTGTAGCCAG | 5336 |
| rs540043389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914037 | GTGCCTCTGCCCTTT[A/G]CTCTTTCCCCTAAGC | 5336 |
| rs540049149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791610 | ATCTCTGTCACCCAG[A/G]CTGGAGTGCAATGGT | 5336 |
| rs540069827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783893 | CTTAAAGCCAGTTCC[G/T]CCTGCTTCATCTTTT | 5336 |
| rs540088678 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804852 | GGATGAGAGAGTGTT[C/T]TTGAAAGCTTGGGAG | 5336 |
| rs540099159 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832789 | CATTCTTGCAAAGCT[A/G]GAGAATGAGGCAGAG | 5336 |
| rs540102881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833144 | CCATTCCTTCCCTGA[C/G]TCTGGTCTGTGAGAA | 5336 |
| rs540109281 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790310 | CAGGTTTTCAGAAGA[A/G]GGATGACGTGATTGG | 5336 |
| rs540109494 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795694 | TACCTGTTTCCTCCC[A/C]CCTGCTTTTTTTTTT | 5336 |
| rs540112287 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835523 | GGTGGAGGTTGCTGT[G/T]AGCTGAGATTGTGCC | 5336 |
| rs540113715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791392 | GTCATGTAATATAAA[C/G]AAGCAGATTTGTGGG | 5336 |
| rs540126525 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790921 | GACAGTCCGCACCAC[A/G]GAGAGTGATCCAGCA | 5336 |
| rs540130140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783432 | TGCTACTTTCTATCT[G/T]TGTGACCTCGGATAA | 5336 |
| rs540133329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870535 | CTTCCCTTTTGGGGC[G/T]CAAAGGAGGGTCTTA | 5336 |
| rs540155775 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894572 | CATGGGTGCATTTGG[C/T]TGAGAAAAGGCAACA | 5336 |
| rs540160990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883553 | GAAACTCTGGATGAG[A/G]AGAGCCTCATGTCGG | 5336 |
| rs540168234 | snp | A/G | 5.01676e-05 | 0.00500812 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910494 | GCCTGCGTTCTCCCA[A/G]CACTGATGGCGTCCT | 5336 |
| rs540168362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905703 | TCACTCTGTCGCCCA[A/G]GCTGGAGTGTAGTGG | 5336 |
| rs540174361 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836794 | CAAGTTCTGGCTCAA[C/G/T]CATTGTGACCTTGAA | 5336 |
| rs540177956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847906 | GAAGATCCTGGAACC[A/G]ATCCCCAACAGTCAC | 5336 |
| rs540188904 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946366 | ACTTAAGCCCATTCA[C/G]AATTGTCTAGCCCAA | 5336 |
| rs540207874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942442 | TAGCTCCTAGCAGTG[C/T]CTGGCACATCCATAT | 5336 |
| rs540208257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821198 | GCCGTGCCTGGCCAC[A/G]TTACCCGCTTTATCA | 5336 |
| rs540210993 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894231 | GCCAAGAGTTTGAGA[C/T]CAGCCTGGGCGACAT | 5336 |
| rs540215386 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878982 | TCCGGGCAGGGAGTT[C/G]CAAGACCTGGCAGAG | 5336 |
| rs540224698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842305 | AGGAGCCCCAGTGTG[A/G]ACTCTGTTGCACTCC | 5336 |
| rs540248947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877324 | AGCTGGGCATAGTGG[C/T]GGGTGCCTGTAGTCC | 5336 |
| rs540252265 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934883 | CTTATAAAACCATCA[A/G]ATCTCGCGAGACTTA | 5336 |
| rs540258792 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916535 | AAATATGTATACATG[A/G]TGAAATGGCTAAATT | 5336 |
| rs540262820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922216 | AGAGCTCCTAGAACC[C/T]ACATTGCTTCTTATG | 5336 |
| rs540266659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820761 | GAGTAGCTGGGATTA[C/T]AGGTGCACACCATCA | 5336 |
| rs540268060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951608 | AAAACTGGAGAAAGA[C/T]AGTACTCCTAGCTTT | 5336 |
| rs540268503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824908 | GACCCAGGTAGGCCC[A/G]ATGTAATTACAAGGA | 5336 |
| rs540281968 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952870 | CCAAAAGTGTCTTCC[A/G]CCAAGAAATTTATCA | 5336 |
| rs540284582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880272 | AGGATATAGAAAAAG[C/G]TATGTGTACCCCAGT | 5336 |
| rs540291375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826452 | TTGAGGTCAAAGTGC[C/T]CGACCTCGTGTGCCT | 5336 |
| rs540340992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934322 | ACCATATTAAAGATC[C/T]GAGTGTGCAAGAAAG | 5336 |
| rs540345259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810392 | CTATGCTTGGCCTTC[A/G]TTATTTGCAGCATCA | 5336 |
| rs540349751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863236 | CCCTGGAAATCACCA[C/G]TCTACTGTCTGTCTC | 5336 |
| rs540351710 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858865 | TCTAGCTTTTTGGGG[A/G]TTAAATGACTATCAT | 5336 |
| rs540352589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802358 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 5336 |
| rs540355846 | in-del | -/CGGTGGCA | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829934 | GCTTATTCTACCTCT[-/CGGTGGCA]CGGTGGCATCCCCAC | 5336 |
| rs540359690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876739 | AAGGTCCTGGGATGT[C/T]GCCCAGAGTGACATA | 5336 |
| rs540362916 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829175 | GTGCAGTGGCACGAT[C/G]TCGGCTCACTGCAAC | 5336 |
| rs540382411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947588 | CAGACTTTTCTGAGC[A/C]AATGATTGATCCAGT | 5336 |
| rs540395820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938613 | GGCTGATGCTGAGGA[A/G]CTGTGGGATCTACCA | 5336 |
| rs540405889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886727 | CTAGAAGCCTCTCCT[C/T]TGTTTCCCCATTTAT | 5336 |
| rs540409731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909863 | TGTTATCATTCCTGT[C/T]AGACCGCTGGGGTAG | 5336 |
| rs540424549 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962473 | CTGCCTCTCAGAAAT[G/T]TCCACATTTCTTATT | 5336 |
| rs540433984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786801 | AAGCAATTTTCAGTT[A/G]CAAATATTTGCTCTA | 5336 |
| rs540434694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836211 | CTGACCCAATCCCTG[C/T]ATTTCTCAGAGGGGG | 5336 |
| rs540442690 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817918 | TGTTTCGGGGAGAAG[A/C/G]GGGTTAAGTGAACAC | 5336 |
| rs540449437 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836416 | TGGATCTTGGCTTCT[C/T]GTTTCATCCTTCCCT | 5336 |
| rs540457347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895551 | GGCAACAGAGCGAGA[C/G]TCTGTCTTAAAAAAA | 5336 |
| rs540462531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822123 | ATTTTATCCTCTGTG[C/T]TTGCCCTAGAGCTTG | 5336 |
| rs540478613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817512 | CGCCTTTTGTCAGCT[A/G]TGTTTGGTGTTGCTA | 5336 |
| rs540494306 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846741 | AATCCCAACCAAAAT[C/G]TAATAGAGATACAAG | 5336 |
| rs540496855 | in-del | -/GCTGCTGCT | 0.00160804 | 0.0283096 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834592 | CCCTGGATCTGCAGA[-/GCTGCTGCT]GCTGCTGCTGCTGTT | 5336 |
| rs540496996 | in-del | -/TTCC | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823961 | CCTTTCCCTTTCCCT[-/TTCC]TTCCTTCCTTCTTTT | 5336 |
| rs540510757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923433 | GGAACGCAGCCGCCT[C/G]CCTCCCCTCCTGTCC | 5336 |
| rs540517994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874557 | CTGGCTGGAAGCACA[A/G]GGCAGAGAAAAGTAC | 5336 |
| rs540522878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927185 | GAAAAGCAGGTGAGT[C/G]CCCCTCTTCGATCCT | 5336 |
| rs540531101 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833251 | TTTACCTTTCTGTGG[A/G]GGCCACAGCCTGGTT | 5336 |
| rs540541717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821556 | TGAGGTGGGTCCTGG[G/T]GGCTCCTGGCTGCTC | 5336 |
| rs540552809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877546 | GGCAGGGCCACACCC[C/T]TCGGAAGGCTCCAGG | 5336 |
| rs540561189 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878194 | TTTCACTGTGTTAGC[C/G]AGGATGGTCTCCATC | 5336 |
| rs540577659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852163 | CTTTCTTCCATGGTA[C/G]ACAAGGTGGTCCCTG | 5336 |
| rs540580550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946678 | CCATAAATTAATCAC[C/T]CCCCAAGCTGAGCAT | 5336 |
| rs540582534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890110 | GCCATGCGAACGCCC[A/G]AAAAGACGTCTCAAA | 5336 |
| rs540587823 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933561 | GCCTGGAGAGTAATT[A/G]TCATGCTGTTTTTTG | 5336 |
| rs540589371 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961192 | GGAAGAATTCAGTGA[C/T]TCTGCTATCATAAAG | 5336 |
| rs540613389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955771 | CGTCTAGTTGGCCTT[C/G]CTTGGGTCATGTGCC | 5336 |
| rs540635572 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959526 | AAAGCCATTTACCTC[A/G]CTTGAAGCCAGGAAC | 5336 |
| rs540644138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828975 | GTGGGCCATTCTCTC[A/C]AACATTGCTAGTCTC | 5336 |
| rs540646914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902280 | TTCCTAGGTATTTCA[G/T]TCTGTTCCTGCAGCT | 5336 |
| rs540658062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932200 | TTTTGGGAAGGTGTG[A/T]GCTTCTGGATAAGAA | 5336 |
| rs540676826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880117 | ATGGTGGCGCATGCC[C/T]GTAGTCCTAGTTACG | 5336 |
| rs540678496 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810764 | TCTATGGATCATTTG[C/T]TCAGGGCAAAGCACT | 5336 |
| rs540680790 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810631 | TTAGTGCCTTATTTT[C/T]TGCAATTTCTTTCTT | 5336 |
| rs540689952 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962926 | CTTGAGTGCTCTTCA[A/G]TTTATCAGTTTTGAA | 5336 |
| rs540691603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785378 | TCTCTAGGGTTTGAA[C/T]GTGAAGCTGCCAAGA | 5336 |
| rs540698133 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959179 | TTTACAGCTGATGGG[A/T]AAAGGAGTGTAACTG | 5336 |
| rs540700669 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962691 | TCTGAATGAATATAG[C/T]AATCTGCCCAGAACT | 5336 |
| rs540705735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856852 | TAGTGGAATCACAAG[G/T]GTTCTTAGATACCCG | 5336 |
| rs540712730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832861 | CCATTAGCCATAAGA[C/G]AGCAGGCTAAGTGCC | 5336 |
| rs540725737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931876 | TCTGGTTGTCTGGTT[C/T]GAACCTTCAGAAGGC | 5336 |
| rs540733211 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939038 | TTTTCTTTCCTCCCT[C/G]TTGCCCACATGGTTC | 5336 |
| rs540738130 | snp | C/G | 1.66147e-05 | 0.0028822 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936396 | AAAGGCCGACTGAAG[C/G]TAGTCCCGTCCCTGC | 5336 |
| rs540773577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836512 | TTGGGAGGGTGAGGT[A/G]GGTGGATCACCTGAG | 5336 |
| rs540785450 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931938 | TCTTTGCGGCCCTAC[A/G]TATCTTACCAAGGAA | 5336 |
| rs540792657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860417 | GTAAATTCTCAGAAA[C/T]GAATACCAGCAGCAC | 5336 |
| rs540797477 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819731 | CTGGGATTACAGGTA[A/C]CCACCACCATGCCTG | 5336 |
| rs540797512 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824210 | GTGATCTCAGCTCAC[C/G/T]GCAACCTCCACCTCC | 5336 |
| rs540824922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800323 | CACCTAGATATTAAG[A/C]CCTGCATGTATTAGC | 5336 |
| rs540836341 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858587 | TATTGGAGTGAGTGG[G/T]GCATTGGACTCGAGA | 5336 |
| rs540836371 | in-del | -/AAAGAATAAAACATTCTGGTTTATC | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950959 | AAAATAAAAGGATAA[-/AAAGAATAAAACATTCTGGTTTATC]AAAGAATAAAACATT | 5336 |
| rs540841666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868902 | GGGCATCACTGTACG[C/G]TATAAATCTCTTATG | 5336 |
| rs540853766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826288 | CTGCCACGGCAAGGC[G/T]CCAGGATCCTAGGCT | 5336 |
| rs540858809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823923 | TTTCCTTCCATCCTT[C/T]CTTCCTTCCTTCCTC | 5336 |
| rs540867230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918943 | GCTAGTTGAGTCACC[A/G]AAGACAAGATTTAAT | 5336 |
| rs540892287 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852377 | CTTGTGGTTGAAGGT[G/T]GTGGGGGTGAATCAG | 5336 |
| rs540892926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897020 | CAGGCTTTATGGGCC[A/C]TGTGGTCTCTGTTGC | 5336 |
| rs540898014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848468 | ATTCTTTCTTTCTTA[C/T]CATGCTCTGTCTCTC | 5336 |
| rs540904234 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778882 | CTCATTGCTGTCTCG[A/C]ACTCTCGAGCTCAGA | 5336 |
| rs540905985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899516 | GTGGGAAATGAGACT[C/T]ATGCGATGCACACGT | 5336 |
| rs540916172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875893 | AGTGATGAGCGTTCT[C/G]TGACGATGTTTGTGG | 5336 |
| rs540965735 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81779357 | AGTCGGGACGCGGGC[G/T]GCGCGCGCGGGACCC | 5336 |
| rs540975207 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848500 | GCCTTTGTACATGTG[C/T]GTTTGCATTTCTCTC | 5336 |
| rs540989009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928429 | TCCCCATGGACGTAT[C/T]TGGTAATGAAAATGC | 5336 |
| rs540994347 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894084 | CTGGGTCCTAGGTGT[A/G]CACAGGTACCGCGTA | 5336 |
| rs540996999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801436 | TGTTTTTGCTTGACC[C/T]TGTGAAGATTTTCCA | 5336 |
| rs541005644 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889395 | GATGTTGCCTCGACT[C/G]ACTGGTTAGCTGGGA | 5336 |
| rs541005801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796732 | GCCATGTGAAGACAG[A/G]TACAGAAATCTGAGT | 5336 |
| rs541011203 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857056 | GACTTCTGGCCTCTC[G/T]AACAGTCTGAAAATA | 5336 |
| rs541024704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853369 | AAAAAAACCATTAGA[A/C]CCTGAACTGGTACAG | 5336 |
| rs541024988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903868 | CTCTGCCCCACACCT[A/G]ATACGCTGTGGCCCA | 5336 |
| rs541033645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882099 | CAGGGCATGTTTCAT[C/G]TCTTACACTATTTGA | 5336 |
| rs541034586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839536 | TGCATACCATGAGTA[C/T]TATTTTATATCTAAT | 5336 |
| rs541044221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885611 | CTTCTGTATGTTTCT[C/G]TCACAGATAGAACTT | 5336 |
| rs541047967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860845 | GCATGGTAGCACGCT[C/T]CTGTAGTCCCAGCTA | 5336 |
| rs541048416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816720 | TTGTCTAGGCTGGTC[C/T]TAAACTCCTGGGCTA | 5336 |
| rs541051239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834906 | AGGCAGCCTTGGTCC[A/G]TTGTAGAACTGGGTA | 5336 |
| rs541071022 | snp | A/G | 0.000661023 | 0.018168 | missense | PLCG2 | GRCh38.p7 | 16:81912694 | AAGCGAGAGGGGAGC[A/G]ACTCCTATGCCATCA | 5336 |
| rs541076578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885266 | TGGCCTCAGGTGATC[C/T]ACCCGCCTTGGCCTC | 5336 |
| rs541078293 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960719 | CAGCCGGACAACATG[C/T]TCTAATACTTCGTAT | 5336 |
| rs541092708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912033 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 5336 |
| rs541103928 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777843 | CAACATAGTGAAACC[A/G]CGTCTCTAGTAAAAA | 5336 |
| rs541104273 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81895629 | GCTGCACTTGCATTA[C/T]GTAAGCGCACAGGGA | 5336 |
| rs541106921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785104 | AGATCCTAGGAGGAG[C/T]CGGTGAAAGGGTGAG | 5336 |
| rs541109988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945710 | GATCAATACTGCTAT[C/G]AACTACTAAGGGACA | 5336 |
| rs541110708 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834488 | TTCCCCTTCTGCAAA[A/G]TGGAGTTGATGATAA | 5336 |
| rs541128585 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914261 | CACAACCGGATCGGG[A/G]CCTCACCTGATGATG | 5336 |
| rs541155391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907347 | AAATAAATATTGAAC[A/G]TAAGGTCTCCAGACA | 5336 |
| rs541167459 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805416 | AGGCAGGAGAATGGC[A/G]TTAACCCAGGAGGTG | 5336 |
| rs541168581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789296 | CGGATGCGCTCTCTC[A/G]CTCTCTGTTTTAGAG | 5336 |
| rs541173414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945446 | AAAGATACTGTTAAC[C/T]ATGGTTCCTTTTAGG | 5336 |
| rs541174053 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838332 | CCTCATGTGATCTGC[C/T]TGCCTTGGCCTCCCA | 5336 |
| rs541175023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816002 | GGGAGGTGGAGGTTG[C/T]GGTGAGCCGAGATTG | 5336 |
| rs541177643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901542 | GTTTCACAGACCCCC[A/G]AAGAATCCACGGTTA | 5336 |
| rs541179492 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904893 | GGCTATTTTTACTTA[C/T]TTATTTTTTACTGGG | 5336 |
| rs541180877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897499 | ATAGAGTAACTGTTG[A/G]GTCAATAAGATCGAT | 5336 |
| rs541185574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832110 | TGATAAATGGAGGGG[C/G]GGAATAGTGATATTG | 5336 |
| rs541204865 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885725 | TGCATTTGGATTTCA[C/T]TGATGGAAGAGAAAC | 5336 |
| rs541206472 | snp | C/T | 0.000399281 | 0.0141238 | missense | PLCG2 | GRCh38.p7 | 16:81921268 | AAATCAATCCGTCCA[C/T]GGTACGGTGCCGAAC | 5336 |
| rs541223238 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797948 | CAATTATTCTGCCTC[A/T]GCCTCCTGAGTAGCT | 5336 |
| rs541241825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904572 | TCCCCATTGGGTCCC[C/T]CGCCACCCTGCCCAG | 5336 |
| rs541251766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901121 | TATAGTTCATTTGTT[C/T]ATTGGTGAACCTTCC | 5336 |
| rs541258477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954320 | AGGCACTGCGCCCGG[C/T]GACTTGATTCTTTTC | 5336 |
| rs541265977 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956220 | TCATCCACCTTGCAG[C/G]TTGTTACCTTGCCTT | 5336 |
| rs541284096 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961883 | AGAGATTTTCAAAAT[C/T]CACTTAAGAGTATCT | 5336 |
| rs541299682 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850526 | GCTCTCAGTGTGATA[C/G]AAATTGACAAGAGGT | 5336 |
| rs541312801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781935 | GGAGTGCAGTGGCGC[C/G]ATCTCGGCTCACTGC | 5336 |
| rs541316329 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806307 | TCCATGTGGCAGGTA[C/G]TATGATCATCATAGT | 5336 |
| rs541364608 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911560 | CTCCCACCTCAGCCT[C/T]CTATCTGGGACTGCA | 5336 |
| rs541366837 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785594 | GGAGATTAGGGGTGA[A/G]AGGTGGGAGCCAGGC | 5336 |
| rs541380971 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812950 | CTTTCCCCGTTGCTT[G/T]TTTTTGTCAAGTTTG | 5336 |
| rs541395350 | in-del | -/TTTTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825294 | CTAATTTTTTTTTTT[-/TTTTG]TTTTTTTTTTTTGAG | 5336 |
| rs541396247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876252 | AGGCTTGAACTCCTG[A/G]GCTCAAGTGATCCAC | 5336 |
| rs541397972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865922 | TGAGCTCCACTGGGG[C/T]ACCAGCATGAGAGGA | 5336 |
| rs541398975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812482 | TTGGCTGCATAAATG[C/T]CTTCTTTTGAGAAGT | 5336 |
| rs541407171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912984 | ACATGACCATGATCC[A/G]TGTTTCTCAGAGGAG | 5336 |
| rs541409883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937223 | CTTTTGGTATGACTT[C/G]GCTGAGTTTTGTTGA | 5336 |
| rs541410798 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960129 | CCTGGTGCTACAACC[G/T]GAATCCACCATGAGA | 5336 |
| rs541425362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790173 | AATTCATAGTGTGTG[A/C]CAGGCACTCAGTTGT | 5336 |
| rs541439492 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815139 | AATTTAGGCTTAAAA[C/G/T]GAAGCACCTGTGATA | 5336 |
| rs541440637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917330 | CTGATTCTACACCTT[A/G]GCTATGGTGAATGGT | 5336 |
| rs541473914 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944489 | TATTTAGAGACAAGG[A/T]CTTCCCTCTGTCACT | 5336 |
| rs541473975 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961796 | AACATGTAGTGTCTA[C/T]GGTATGCCAGCACTT | 5336 |
| rs541485566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865654 | GGGCTCCTGGGGGGC[C/T]CTGGCCTCTTCCTTG | 5336 |
| rs541486216 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945543 | AGCCAGCAAACCAAC[C/T]TTTGAGATGTGTTGC | 5336 |
| rs541487178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781821 | AGAGACAAAAACTTC[C/T]TTGATTTCTGGTTTT | 5336 |
| rs541497361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853628 | GCTGCTGATCTGACA[C/G]TTGGTGGAGCTCAGA | 5336 |
| rs541506109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916930 | GGTGTGAGCCACCAC[A/G]CCCGGCCAGGACTTT | 5336 |
| rs541510465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794371 | TAAATGAATTATTTT[C/T]TCGCTGGCATCTCCT | 5336 |
| rs541544088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861356 | CTTCGTGTCTGGTCA[A/G]TGTCCTCTGTTACTT | 5336 |
| rs541544147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857091 | TATATTACTTTAAGT[C/T]ACTAAGTTTGTGGTC | 5336 |
| rs541556743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878945 | TGCCAATGAGCTTCC[A/G]GTTGCTTCAACAAGC | 5336 |
| rs541572384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828071 | CTCCAGCCTGCGCAA[C/T]AAGAGCAAAACTCCG | 5336 |
| rs541573498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793953 | CTTCTCCTAAATGAT[C/T]TCAAAGACGTATCAG | 5336 |
| rs541583343 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931129 | TTCCTGCATCTTAAG[C/T]GTCCCTCTCCTTTCT | 5336 |
| rs541584860 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925131 | CTCTGACAGGCAGTT[-/C]TCTGAATTTCGAAGG | 5336 |
| rs541588613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820681 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCCCAC | 5336 |
| rs541593490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882130 | AATAGACCTCTTTTC[C/T]CCAGGCTCCTGCAAG | 5336 |
| rs541607252 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958792 | TGGCCCTACTGAACT[A/G]GCTGGGAGGCTGCTG | 5336 |
| rs541609366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854350 | CTGTTGGGGAAGGAA[A/G]GAGCCAGGCTGTGCC | 5336 |
| rs541631027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831767 | TCTTGCCCCAATCCT[G/T]CCTTGTCTGAAAGGG | 5336 |
| rs541635456 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945504 | CCGTTCTGTTTCAGC[A/C]CTGTGTTCTTTTATA | 5336 |
| rs541636675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805663 | CTTTGCCATCCATGT[C/T]TCCATCCTGCAGTAG | 5336 |
| rs541649696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820287 | GGAGAGAGGGTTCCC[C/T]CACTTCCCTCTGCAG | 5336 |
| rs541661136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879492 | AAGAAACACACACCC[A/C]CACAAACTGATGTGG | 5336 |
| rs541673260 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836178 | TTTCATACCCTAGAG[A/G]CTATCCAAATGACAC | 5336 |
| rs541676855 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926727 | AGCCTGTCTGCCTCC[A/G]GAACCACCTTCTCTC | 5336 |
| rs541682193 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933726 | AGAGCTAAGCACCCC[C/T]CAAACAGTCACCATT | 5336 |
| rs541700940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809669 | GGGACTTGCTGTTTT[C/T]TCTGTTCCCTGCGGT | 5336 |
| rs541717223 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799700 | CAGGTTCACACCATT[C/G]TCCTGCCTCAACCTC | 5336 |
| rs541719836 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921396 | GGCCAAAATAATTTT[C/T]TTTTTTTTTTGAGAA | 5336 |
| rs541722735 | snp | C/G/T | 3.35302e-05 | 0.00409441 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937732 | CTCATGCCTGACTTA[C/G/T]AGCAGGCGTTCACTT | 5336 |
| rs541730042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893400 | TTCATCTTCTGCAGC[C/T]TTTTTTGCTTCTGAC | 5336 |
| rs541737059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908917 | TCTCACTCACTTTCC[C/G]CGATCCCAGCCCTGG | 5336 |
| rs541743659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933224 | TAAAGTCCTGTTATT[A/G]CATCTGAGGGGTAAA | 5336 |
| rs541763771 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874638 | CTGCAGGAGACAGAG[C/G]TATTTATGGTGACTT | 5336 |
| rs541783129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925296 | TGCATACTTCCAAAC[G/T]GGTTCCCTGTAGCTA | 5336 |
| rs541785083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949635 | AGAAAAGAAAACTTT[C/T]AGATAGGGAGGTGAA | 5336 |
| rs541800972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901162 | TCGGAGACAGCCCCA[C/T]GCGAGGTGCTGGAGG | 5336 |
| rs541808695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853918 | GGGTTGGCCTCTTAT[C/T]ATTATTTTTAATTTG | 5336 |
| rs541815786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862199 | GAGCCACAGAGGCAG[A/C]GGAAAGACTGAAGGC | 5336 |
| rs541816980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879087 | CTGAGTGGGGGAATG[C/T]GGTGCGGGCTTTTTC | 5336 |
| rs541820655 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815114 | GTTATGGAAGGAATG[A/G]TAATTGGGGAATTTA | 5336 |
| rs541837533 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958282 | CATTGAATAAAAGCA[A/G]TGAAAACCTTGATCA | 5336 |
| rs541846783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882664 | TTCCTCCCCTCCCTT[C/G]TCTTTTTTCCTCGAG | 5336 |
| rs541849846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957797 | TCTCTGAGTCTCAAC[A/G]TCTTACCAGGAACTT | 5336 |
| rs541853084 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802392 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 5336 |
| rs541861739 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835183 | TTTTATGTCTGCAAA[A/G]TGGGTATAATAATGA | 5336 |
| rs541895353 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961927 | TAAGATTGCTGATCG[C/G]ATGTGAGGGCGATCT | 5336 |
| rs541899254 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851967 | GCCTGTGAATGGCCA[C/T]GAACCTCTCCTGTGT | 5336 |
| rs541901834 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866512 | GCATGAGAGGACGCT[A/G]GCCTCTCCCTTGCTC | 5336 |
| rs541907309 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961475 | AAATTTTAAAGGCTT[A/G]CAGCCTTAGGATTAT | 5336 |
| rs541919871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890016 | GGTGCTGCTGATTGG[C/T]TGGAGATGCAATCAT | 5336 |
| rs541923192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808642 | GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC | 5336 |
| rs541925580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831042 | TTTGCTCTGCCTGAA[A/G]TATTCTATCTCAGAC | 5336 |
| rs541953281 | in-del | -/TCTGGGG | 0.00522925 | 0.0508653 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873992 | AAAATGTCAGAACCC[-/TCTGGGG]TGCCCTAGATTGCCC | 5336 |
| rs541957415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942060 | TTGGTACACCTTTAC[A/G]TTCCTAGCCTTGACG | 5336 |
| rs541975525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898408 | TTTGTTGTAAAAGCT[G/T]TTTAGCTGTTATGTT | 5336 |
| rs541976457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869631 | AATGAATGCATGTAT[A/G]TCTTTTGGAAAATAT | 5336 |
| rs541986872 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850848 | GGACTGGTCATTCTT[C/T]AGATCTCCTGCACAT | 5336 |
| rs541989103 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834959 | TTGCTGTAATCTGCT[A/C]TCTGGAGAACAGACC | 5336 |
| rs542001638 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864638 | AATATGTGAAGGGTG[C/T]GTGGACCTGCCTGGC | 5336 |
| rs542001743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794873 | ATTGTCCTGCTCCCC[C/T]TGGAGTATGTGTCCT | 5336 |
| rs542008596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955340 | TCAACAGATGTTTTT[A/G]TAGCACAGGAGTCTT | 5336 |
| rs542011868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902217 | GGAAGGAGCGAGTGT[A/G]AATTTTGTTGACATT | 5336 |
| rs542030037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843186 | TTTGAGAATAAAGTG[G/T]TGTTTCAGTCACTAT | 5336 |
| rs542030231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877271 | CATCCTGGCTGACAC[A/G]GTGAAACCCTGTCTC | 5336 |
| rs542031871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847277 | TCTGGGCATGCCACC[C/T]GCCAGAAACTTCCAT | 5336 |
| rs542035267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828520 | TGGGATTACAGGCGT[A/G]AGCCACCGCACCCGG | 5336 |
| rs542053126 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933782 | CCCCCTTGGCCAATA[A/G]AAGTCTGATAGAATT | 5336 |
| rs542053577 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919202 | CCCTAGGAAGCTCCT[A/G]AAGTCAAGTCCTGTA | 5336 |
| rs542070328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798461 | AGTGCTTCTGGGAGG[C/T]TGGGGAGGCCTGGGC | 5336 |
| rs542073528 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905347 | GAAGGCTGCTGGCTC[A/T]AAGGCCTAAACTTGG | 5336 |
| rs542081966 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958860 | GTCAACTGCTGCTTG[A/G]AAGAGGTAGACAAAA | 5336 |
| rs542097004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824227 | CAACCTCCACCTCCC[A/G]GCTTCAAGCAATTCT | 5336 |
| rs542097101 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81917807 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 5336 |
| rs542119112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850888 | AGGGTTAACTCCCTT[C/G]AGTAAGATTTAAGAT | 5336 |
| rs542130493 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879802 | TGGTGCAAGTAGAAG[C/T]TGGAGGGAGGGGTGC | 5336 |
| rs542142158 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900516 | CGAGCAGCGCCCGGT[G/T]TCTGTCGTCCCAGGG | 5336 |
| rs542147498 | in-del | -/GAAAT | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950016 | TTGAAAAACAGACAA[-/GAAAT]GAAATAAGGAGGAAA | 5336 |
| rs542153059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882965 | TCACCTGTCTTCCCC[A/G]TGGCCACACTCCTGG | 5336 |
| rs542159195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831842 | GGAGGCCACGCTAGC[A/C]ATCCCCCAACTTTGG | 5336 |
| rs542162565 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905834 | CTGGCTAATTTTTTG[-/T]ATTTTTGCAGAGATG | 5336 |
| rs542163099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855168 | ACTCCCCTACAGTCT[A/G]GGTGACAGAGCAAGA | 5336 |
| rs542167736 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81798845 | CCTCAGGACTTCAGG[A/G]ATCCCACTGCGTCTT | 5336 |
| rs542170351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937979 | ATGCTGTCTTGAGAG[C/T]AGGGAACCCATGTCT | 5336 |
| rs542172080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809963 | CTTCATCTTTCTGCC[A/G]GTCTTTGTCTGCCAC | 5336 |
| rs542182217 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920351 | ACTGTTCTAGATACT[A/G]GGAGTACTGTGGAAC | 5336 |
| rs542187065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897579 | GAGATGGAGTCTCCC[G/T]CTGTCGCCCAGGCTA | 5336 |
| rs542187172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901493 | CCCCCGCATTCTGCT[C/G]TAGCATCTCTCAGGG | 5336 |
| rs542203657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857918 | AAAAACACTTAGAAC[A/G]ATGTCTAGTATATAT | 5336 |
| rs542210702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784151 | CTGGCATGGCTGACC[A/G]AGGAGGTCCCTTTGG | 5336 |
| rs542211895 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887902 | CTAGAATGTCTAGGA[C/T]TGTGCAGCAGCTGCT | 5336 |
| rs542238227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884039 | TTGCACAGGGCAGCC[C/G]CCCCTACCCCCCAGC | 5336 |
| rs542238456 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888040 | TTTGGAGCTGAGACT[C/G]TGCAGTTTACAAGCT | 5336 |
| rs542247876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913333 | TGTTGAGTTCCTAAC[C/T]GTGTTCTAGACACTG | 5336 |
| rs542251735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911135 | CAAGGTAGGTCTTGC[A/G]AAGGGTCAACAAATT | 5336 |
| rs542275351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887680 | TCCAGCCCTTCCCAT[C/T]TAAGCACACACACAT | 5336 |
| rs542275540 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839921 | GTAGGTGTGATGGTG[C/T]ATGCCTGTAGTCCCA | 5336 |
| rs542291840 | snp | A/G/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866043 | CACTGGGGCACCAGC[A/G/T]TGAGAGGACGCTGGC | 5336 |
| rs542293515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943774 | ACAAAAATCACATTG[C/T]AGCGATAGGGAAAAA | 5336 |
| rs542315149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841472 | TTTCAAACTCCTGAC[A/C]TCAAGTGATCTGCCC | 5336 |
| rs542321724 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889843 | TTGTATTTTTAGTAG[A/G]CAGGGTTTCACTATG | 5336 |
| rs542324064 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81891098 | AACCCAGGAGGTGGA[A/G]GTTGCAGTGAGCTGA | 5336 |
| rs542341553 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867745 | CTCTGTCACCCAGGC[G/T]GGAGTGCAGTGGCGT | 5336 |
| rs542357540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889517 | ACAGAACCGATTGAT[C/T]AAGGCAGGGGAATTG | 5336 |
| rs542359757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824975 | AGAGAGAGCAGGATT[C/T]TGGCTTTGAAGGTGG | 5336 |
| rs542365317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903423 | AGAGCATCAGTGCAC[A/G]GGGAGTGTTTGGCCA | 5336 |
| rs542365359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899886 | ATATTGATTCATTGA[G/T]GAAAATGTTGTGACC | 5336 |
| rs542366284 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906958 | CAGGAGAATTACTTG[A/C]ACCCGGGAGGCGGAG | 5336 |
| rs542385006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790324 | AGGGATGACGTGATT[C/G]GATTTGCATCTTTGA | 5336 |
| rs542416532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877174 | AAAAATAACAGAAGT[A/G]TCGGGCACGGTGGCT | 5336 |
| rs542427127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901918 | TTATGCATTATTATT[C/G]TGAGAAAAGGGTCTG | 5336 |
| rs542432066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802632 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 5336 |
| rs542434788 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960461 | TCCTAAGTGTGTTAT[A/T]TAGAATATTGGTTAT | 5336 |
| rs542443236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854763 | GGTGAGTGACTTAAC[C/G]TCTCTGAGCTGCAGT | 5336 |
| rs542448043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957024 | GGCTCACAGGCCAGG[C/T]ATGGTGGCTCATGCC | 5336 |
| rs542451943 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852874 | GCTGTTGGCTGGGGG[A/C]TCAGCTGGGCTGTTG | 5336 |
| rs542473322 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960216 | TTCTTGGTGGTGTTA[A/G]GGACTGATTCTCTCA | 5336 |
| rs542474315 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878236 | TGATCCGCCTGCCTC[A/G]GCCTCACAAAGTGCT | 5336 |
| rs542480105 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806516 | TTCTTGGGGGTTGCT[A/T]TTGACCCAGGCAGCA | 5336 |
| rs542488758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856282 | GAGGCTTCATAGTTC[C/T]ATGAGGTGTTTGCAC | 5336 |
| rs542496064 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879083 | CTCCCTGAGTGGGGG[A/C]ATGCGGTGCGGGCTT | 5336 |
| rs542501979 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779966 | GTCTGCGTAATTATG[A/C]GTGTGTCTGTGCGTG | 5336 |
| rs542503452 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934915 | TCAGTACCACAACAA[C/T]GGTACAGGGGAAACC | 5336 |
| rs542503459 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951116 | AGTAGCTGGGACTAC[A/G]GGCATATGCCACCAT | 5336 |
| rs542504631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879754 | AAGATGTGGGTGTGC[A/C]GGGTGCCTGTGTACA | 5336 |
| rs542513977 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864440 | ACCTCAGACAGCACA[G/T]ATGTCTCCATCATTG | 5336 |
| rs542525403 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860525 | CCCTTTCCTGATGAT[G/T]TATTGTGCCATTAGA | 5336 |
| rs542548303 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951324 | AGAGGAAAAACATGT[A/G]AGAGTAAATACTGGA | 5336 |
| rs542554003 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805777 | GTTTTGTTTTTTTTT[G/T]TTTTTGTTTTTTTTT | 5336 |
| rs542562241 | snp | A/G/T | 0.000115916 | 0.00761225 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81858324 | CTTACACCAGGAAGC[A/G/T]ATGAATGCGTCCACG | 5336 |
| rs542590353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916013 | GTACATATTTATACA[A/T]GTCTGTATCTATGGA | 5336 |
| rs542593063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815169 | ATGACGCTCTGGAAC[A/G]CCTCTTCATGCAGAG | 5336 |
| rs542596425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846243 | AGGACAAGAGGACTG[A/G]CCTCCCTTCCTTCAG | 5336 |
| rs542600966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906430 | AATATTTATTTATTA[C/T]TTATTTATTTATTTT | 5336 |
| rs542602302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859696 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTTTGT | 5336 |
| rs542611829 | snp | C/G | | | missense | PLCG2 | GRCh38.p7 | 16:81869227 | AGCATCAGTCTCCGA[C/G]AGTTGAAGACCATCT | 5336 |
| rs542613562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910803 | GCCTGGTGGTTCAGC[C/T]GGGCCAGTCCCCCAG | 5336 |
| rs542627535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841646 | TAAGCCAGAATAGAG[A/G]CTTCTTCATACAGCC | 5336 |
| rs542640555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892345 | CTCTGATTGCAACAG[A/G]AGGAGGATACAGGAT | 5336 |
| rs542645280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915312 | TTCTGGGCTCTGGGG[A/T]TGTGTAATGAACTTC | 5336 |
| rs542668684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891712 | AGGGTGTAGCACCGC[A/G]TTCCTTGGACTAAAA | 5336 |
| rs542682429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849878 | AAAAGAATGTTTGCT[G/T]AAAGTCACTAGACTT | 5336 |
| rs542690221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863879 | GGGTTGCAGGTGGAA[G/T]GCAGGTGGGTGAGTC | 5336 |
| rs542708551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914943 | GATGTTGAACTTCCC[C/T]GGTCTCTACCCACTG | 5336 |
| rs542719443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849413 | AAAAAGTTTTTCTTT[A/G]GTTATGTATAATTTT | 5336 |
| rs542724260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797030 | CGGAATTTAAGAGGC[A/G]TTGCTTTCTTCCACG | 5336 |
| rs542756016 | in-del | -/T | 0.271432 | 0.24908 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797837 | TTCTTTTTTCTTGTC[-/T]TTTTTTTTTTTTGAG | 5336 |
| rs542761259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886431 | TTCTAGAAAACACTT[C/T]GGCTGTATGCAATGA | 5336 |
| rs542788295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845403 | CACTCATTTAATCCC[C/T]ACAAGAGCACTGTGT | 5336 |
| rs542788716 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853465 | ACAGTTTTTCCACAG[A/G]TGGTGGGGGCAGTGG | 5336 |
| rs542799457 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952550 | AAATGGTGGAAGCAC[A/T]TCAAAGGGGCCTAGG | 5336 |
| rs542799607 | in-del | -/GCTGCT | 0.0146788 | 0.0844035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834600 | TGCAGAGCTGCTGCT[-/GCTGCT]GCTGCTGCTGCTGTT | 5336 |
| rs542811647 | snp | A/C | 0.000399281 | 0.0141238 | missense | PLCG2 | GRCh38.p7 | 16:81956813 | ATGCCAACCGGGATG[A/C]CCTGGTTAAAGAGTT | 5336 |
| rs542815121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912103 | CGCCTGGCCCAATTT[C/T]TGTATTTTTAGTAGA | 5336 |
| rs542846766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907958 | GATTGGCTGGCTGCC[C/G]CAGGTGCTTTAACCA | 5336 |
| rs542878500 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911623 | ATTAATTAATTAATT[A/G/T]ATTTTGAGACCGGGT | 5336 |
| rs542880287 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792653 | GAGAAGCCTTCTTCA[C/T]ATGGTGGCAGCAAGG | 5336 |
| rs542915801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849152 | CTTACAGCAATGGGA[C/T]GTCACGGGAAGGCTT | 5336 |
| rs542916986 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794065 | CACATGAATTCCTTA[C/T]GTGTGCAGAGGACTT | 5336 |
| rs542942400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880748 | TGCTTCTTAAGTTTC[A/T]GTTATATTTGAATAT | 5336 |
| rs542943350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931358 | TACCCCGATGGAAAG[C/T]AGACGTCCCCATCAG | 5336 |
| rs542947033 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910191 | CGTCTCCCAGGTACA[A/G]GTGATTCTCTTGCCT | 5336 |
| rs542952782 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868690 | GAAATCACATCATGT[C/G]AACACCTATATTGGG | 5336 |
| rs542960505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846639 | ATGCTTAAAAAGATC[A/G]TGAGTAGATAGTCCA | 5336 |
| rs542963876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859964 | TGCACAAAGCTCTAT[G/T]ACGGACTATTATTAT | 5336 |
| rs542964801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948926 | CCAGTGGAAACCTCA[C/G]ATGATGAGAACTGTA | 5336 |
| rs542972980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896893 | GAGAACATTTAGGTT[C/T]ATTTCAAGGGTTTCT | 5336 |
| rs542977138 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856875 | GATACCCGGGAAGGT[C/G]ATTCCCAGAGAAAGA | 5336 |
| rs542983326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920697 | GAACAGAGAGGTGGT[G/T]GGGGTGGATCTTGTC | 5336 |
| rs542991071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811617 | GAGTAAGAAAATGTG[A/G]TGTTTGGTTTCCTGT | 5336 |
| rs542996386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842301 | GGGGAGGAGCCCCAG[G/T]GTGGACTCTGTTGCA | 5336 |
| rs543006404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780488 | CAGAATTTTGAAGTC[G/T]ATGCCAGCCTCAAGC | 5336 |
| rs543015251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819341 | TATCCATTTTCAGAG[C/T]TCATTTCTGAGGCTT | 5336 |
| rs543020496 | snp | A/C | 4.9689e-05 | 0.00498418 | missense | PLCG2 | GRCh38.p7 | 16:81936326 | AAACTACGACCCCTT[A/C]CGCCTCTGGCTGTGC | 5336 |
| rs543027046 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960535 | TTTGGGAAACTTAGG[C/T]TATAAAAACTAAATA | 5336 |
| rs543037046 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807882 | ACTTTTCAACAGCCA[G/T]ATCTCTCAAGAACTC | 5336 |
| rs543037985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881137 | TGAGCAGTAGCAACA[A/G]GAAGGTGTGGAGCAC | 5336 |
| rs543042741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823435 | CAGGTGAAGATTGAG[C/T]GGGGGTAGGGGCTGC | 5336 |
| rs543050158 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796967 | AGTACAGGGATTGAC[C/G]TACCCATTCAGCCAC | 5336 |
| rs543051436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834223 | TTAAAGAGATGTTGA[A/G]GTCAACTCTGACACC | 5336 |
| rs543075429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801302 | AGAGAAATCAGTATC[A/G]TGATTTAATAATTAT | 5336 |
| rs543077693 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901428 | CATGCGAGGGAGAAT[A/G]TTCTGTGAGTTTTGA | 5336 |
| rs543081900 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859997 | TTTTTTAGAGGCAGG[A/G]TCTCTGTCTGTTGCC | 5336 |
| rs543093534 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940178 | GGAATCACTGTAAAA[C/G]CGATTGGGTGGCTTG | 5336 |
| rs543104059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827011 | TTCTACTTCCAGCCT[C/T]CCTGTTCCCCTAGGG | 5336 |
| rs543114282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853235 | ACTCCTGAGGCTCAG[A/G]CAGGATAATTGTTTG | 5336 |
| rs543120522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924090 | CCCGTGCTGTGTGCA[A/G]TGGCCACATCCTGAA | 5336 |
| rs543136876 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878492 | TTCTATCTTTAGAAC[A/G]TCTTCCTTGATCACC | 5336 |
| rs543137141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875479 | TTAATTTTTGAATCC[C/T]TTGTATTAAAGAAAA | 5336 |
| rs543156823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785453 | CATTTGCCAAAGTCT[C/G]CATGGATGATTCTGA | 5336 |
| rs543168131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864410 | CTCAGCAGCCCCGTG[A/T]GGCTAGCAGCTACTA | 5336 |
| rs543175173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953278 | CCCAGTGAAATATGA[A/G]TAAGATCTGTAGTTT | 5336 |
| rs543192904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812086 | ACGGAGTCTTGCTCT[C/T]TTGCCCAGGCTGGAC | 5336 |
| rs543208167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941256 | TGCTGGCCGGGCACG[A/G]TGGCTCACTCCTGTA | 5336 |
| rs543208701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823440 | GAAGATTGAGTGGGG[A/G]TAGGGGCTGCACTGT | 5336 |
| rs543219866 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849346 | CAGAGCAATTTCAGA[A/G]GTAGAATTGTTAAAA | 5336 |
| rs543228019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827068 | AAGCCCCATGATTGT[C/G]CTGTGGCCTAGGGCT | 5336 |
| rs543229412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849907 | TTTCACTGGCAGTCA[A/G]CTGGGTGGGTGAATA | 5336 |
| rs543237788 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81908856 | TGAACAAAATATGAA[C/G]ATTTTAAACAAAGAC | 5336 |
| rs543238296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953025 | GACGCTGAGAAGGGT[A/G]CATTGCTTCTGTGAC | 5336 |
| rs543238337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957486 | GACTTTTAAGGAGTA[C/T]TTATTGTGTTTCCAA | 5336 |
| rs543241149 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961090 | TTTCCAAGTTTTTCT[G/T]GTGGTTCCAAATTTT | 5336 |
| rs543264405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842634 | GCCCCTTGAGGTCAT[A/G]TATGGGAATTGGGGA | 5336 |
| rs543265692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885285 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 5336 |
| rs543288832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830664 | TGTGTGTGTGTGTGT[A/G]TGTATATATATATAT | 5336 |
| rs543289354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868845 | TTCTCACTGGGACAT[A/C]ACCCTATACTGGGGA | 5336 |
| rs543306302 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888820 | TGGACCAAATATAGC[G/T]GACCACTTGTTTTTA | 5336 |
| rs543348476 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957051 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCTGA | 5336 |
| rs543354244 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836763 | GTGCAAACTTTGGAG[C/T]CTGGCCATTCAGGTT | 5336 |
| rs543354591 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850633 | TTCTCTTCCTGGCTC[C/T]CCGAAGACAGTCAGG | 5336 |
| rs543355016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815745 | TGGAAACCTTTGTAG[C/G]TCTTAAGTGCGCTAT | 5336 |
| rs543355960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931810 | TCAGACAATTGGAGC[A/G]CCTCTTGTTAGAGAG | 5336 |
| rs543374306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804492 | GGCATGGACACTGAT[G/T]GGCAAGGATGTGCTT | 5336 |
| rs543385486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944846 | AGGTCCTGAACGAGT[C/T]CCCCATAGATATCAA | 5336 |
| rs543393326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912130 | TAGAGACAGAGTTTC[A/G]CCATGTTGGTCAGGC | 5336 |
| rs543393414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893296 | TGTTGAATATCTGTT[C/T]TGTGCCTGGCCTCAA | 5336 |
| rs543396017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785097 | AAGTATGAGATCCTA[C/G]GAGGAGCCGGTGAAA | 5336 |
| rs543404897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865282 | GGGTGAAGCTGAGCC[A/G]TTGGCTTCCTCCCCT | 5336 |
| rs543408378 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838237 | GACTGTAGGCACCTG[A/C]CACCATGCCTGGCTA | 5336 |
| rs543411628 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902922 | CCAGATCTCATGAGA[C/T]GTGTTCACTATCACA | 5336 |
| rs543414201 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882148 | AGGCTCCTGCAAGTG[C/T]TCAGGGAAACATACC | 5336 |
| rs543431649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888854 | ACAAAATATTGTTGG[A/C]ATACAACCATGCCCA | 5336 |
| rs543434766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856344 | ACAGAGTAGGGTTAA[A/G]TAACCTCCTGAATGT | 5336 |
| rs543438693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907303 | ACTAAATTTCATCGG[A/G]GGAAAAAAAAAAGAA | 5336 |
| rs543448358 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888606 | CACAGAAACTGTGTG[A/G]TAGATACTCTTATTC | 5336 |
| rs543448930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906980 | GAGGCGGAGGTTTCA[G/T]TGAGCTGAGATTGAG | 5336 |
| rs543461110 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784709 | GAGATACATTATCTT[C/G]TTTAAGCCTTACAAA | 5336 |
| rs543461745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888409 | ATGTTTGTATTTTAG[A/T]AGAGATGGGGTTTCA | 5336 |
| rs543483627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935873 | CTTCTATAACTGTAC[C/T]ACTTTTGTGTTTTCT | 5336 |
| rs543484070 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914603 | GTTAATAGATGTTTG[C/G/T]TGAGCACCTACTGTG | 5336 |
| rs543485239 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793879 | AAGGGCAGAGCTACA[A/G]TTTGAACTTGTTCTT | 5336 |
| rs543496661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916573 | TAACATATACACACA[C/T]TTAACCATTTTTTTT | 5336 |
| rs543503558 | in-del | -/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815120 | GAAGGAATGATAATT[-/G]GGGAATTTAGGCTTA | 5336 |
| rs543513771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911151 | AAGGGTCAACAAATT[C/T]TGGGAATAAAGAAAA | 5336 |
| rs543522084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788816 | AGGTGGCCATCTTCC[C/T]TCTTGACTGTTTGCA | 5336 |
| rs543522897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793552 | GACATTTTCACTTTT[G/T]CTTAGGCATATCTTC | 5336 |
| rs543525934 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883172 | CAGACTAAGTGGGGC[A/G]TTCTGGGTGGCAGGC | 5336 |
| rs543534611 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858730 | ACCTATCACTCCCTC[C/G]TGGGTTGATGAAGAC | 5336 |
| rs543542945 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944416 | TAAAGTAATCTAATT[G/T]AAAGGATATGGGAGG | 5336 |
| rs543545279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793037 | AAATATTGCATAATC[G/T]AAACTTAATACAATA | 5336 |
| rs543561374 | snp | A/G | 0.000376622 | 0.0137175 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900561 | CTCTGTGGGGCAGAT[A/G]CAGAGGTGTGTGCTC | 5336 |
| rs543563928 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777391 | TAACACATACTAAAA[C/T]AAAAGTGTGAAAAAG | 5336 |
| rs543579377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886292 | AAGTGTAGGAAATCT[A/C]TCTCTCTGCATCTGG | 5336 |
| rs543584798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788405 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 5336 |
| rs543591187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841781 | GTTCTTCTGCTGTGT[A/G]TCTCACCTATTCCCC | 5336 |
| rs543603607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857402 | TTAAAATCCTGTATC[C/T]TCCACTGTCTCAGTG | 5336 |
| rs543619326 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853577 | TCGCATGCGTAGTTC[A/C]CCGTAGGGTTTGCGC | 5336 |
| rs543627784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781599 | TGGAATTTACACTCT[C/T]ACTTGCAGTGGCTGA | 5336 |
| rs543630617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928366 | AACCTCCTGGCACCC[G/T]CTCCCCGCCAGGTCC | 5336 |
| rs543639638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801392 | ACATAAAAGACACTG[C/T]GTGGTGTGTATCCCT | 5336 |
| rs543639653 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860662 | ATGATTCAGCTCTTG[A/G]TAATGTAATGATAAA | 5336 |
| rs543651445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957904 | TACAGAGTTCAGCAC[A/G]CAGCCCATTTCTCAT | 5336 |
| rs543664032 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806491 | TTACTGGGTAATCAC[A/C]GTAGAACCTTTCTTG | 5336 |
| rs543670874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839505 | CCTTTATTGCCTTAA[C/T]AATTTTTGTTATATT | 5336 |
| rs543674565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924580 | CTTTTGACTCCAGAG[C/T]TTACACTCTTAACTC | 5336 |
| rs543691025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785523 | TTTTTGTTCTTAATT[G/T]TGCTCAGGAATAAAG | 5336 |
| rs543693805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780888 | AAAAATTACCTGGGC[A/G]TGGTGGTGGCCGCCT | 5336 |
| rs543704880 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808651 | GGTGCCCGCCACCAC[C/G]CCTGGCTAATTTTTT | 5336 |
| rs543711935 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871568 | GTCTCGAACTTCTAA[C/T]CTCAACTGATCGGCC | 5336 |
| rs543719854 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912827 | CAGTGCCCTGCCCCC[C/G]CAGCATCAGCGACAA | 5336 |
| rs543724015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808248 | CAGCCTGTTTTCCAA[C/T]GGGGCTACACTGTTT | 5336 |
| rs543738114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790087 | TGGACTGGAAATAAC[A/G]TTGGTGTCTACCCCA | 5336 |
| rs543744501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835009 | CCATTGCCCACCTCC[A/T]GGTGTCATGAACACT | 5336 |
| rs543750718 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872934 | TGGCCACACAGTGAG[G/T]CCACCTGATGGGTGA | 5336 |
| rs543754999 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843001 | ATGGGTGGTGGGGGT[A/G]GGGTGGACCTGGGAA | 5336 |
| rs543755149 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839017 | CCCTTTATGACTCAC[A/T]GAACCAAGCCGAGGG | 5336 |
| rs543773874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860932 | CAGTGAGCCGAGATC[A/G]CGCCACTCTACTGTG | 5336 |
| rs543789604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895005 | ATAGACTTTCTTCCC[A/G]TTTATGATTTTTCTC | 5336 |
| rs543791653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914092 | GGATGGGGAGGAGGT[A/G]TGTTCAGTCCGCTGC | 5336 |
| rs543805262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815951 | CCTGTAATCCTGGCT[A/C]CTCAGGAGGCTGAGG | 5336 |
| rs543827748 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81852241 | GAGGTTTTACCAGTA[G/T]TCCTGGCCAAATAAG | 5336 |
| rs543848784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846666 | TCCATGTTCATGGAT[A/C]GGAAGACTCAATATT | 5336 |
| rs543849538 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918888 | AGATGAAGGAATGAA[A/C]GACTTGTTTCTTTTT | 5336 |
| rs543862502 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933093 | CACCTCCTCTCCTGC[C/T]GCGTGAAGGTTCCTG | 5336 |
| rs543873430 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941474 | AGAACCAAACTATGT[C/T]AAGGCTGCCTATCTT | 5336 |
| rs543874238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894609 | TTGTCGTGGTGTCTC[A/G]TGCCTGTAATCCCAG | 5336 |
| rs543891653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823800 | GTCCCAAAGTGCTGG[A/G]ATTCCAGGCATGAAC | 5336 |
| rs543894821 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821667 | CAGGAAGTGGCCTCT[C/G]TAGAAAAAAATGTAT | 5336 |
| rs543922931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923088 | CGGCACTGTGATGAC[A/T]GTCTTGGCTTAATCT | 5336 |
| rs543943442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847660 | ATTTAAGCTATGGTC[A/G]ATTGAAAATATTTGA | 5336 |
| rs543944311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898841 | TGTGGGGGATGTCTG[C/T]GCCTTATTTCAGATG | 5336 |
| rs543947598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848041 | GGAAGACATAGACTA[C/G]CAAACACAGCATTGT | 5336 |
| rs543969142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797567 | GGGGACTTCCCAGCA[C/T]CTGGCCCATATCTGG | 5336 |
| rs543969269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801619 | TTACTATAGGATTCT[A/T]CCTTATTTTTTAAAA | 5336 |
| rs543980064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809173 | GCAGACACTCTTGGC[C/G]TGACCTTATCCCCTC | 5336 |
| rs543987157 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859384 | AGTACAGCCTCAGAG[A/G]TGATCTCTGCCATGG | 5336 |
| rs543992202 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813438 | CTTAGTAGCAATTGT[A/G]AATGGGAGTTCACTC | 5336 |
| rs543993225 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918286 | CCCAGACCAATGCTA[C/T]GGAGGTTTTCCTCTC | 5336 |
| rs543994731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859300 | ATCTGCGGATGCCAT[A/G]TTGGGTCCTGGGGTT | 5336 |
| rs543998422 | snp | A/G/T | 6.73893e-05 | 0.00580437 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910747 | AGGGTGGAGCAGGAG[A/G/T]CAGGCGGTGGTCGGG | 5336 |
| rs543998736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937619 | CCCTATATTTTCTTT[C/G]AGTGAGATACCTATT | 5336 |
| rs544010190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910338 | TCAGGTGATCCACCC[A/G]TCTCGGCCTCCCAAA | 5336 |
| rs544020353 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799798 | TGGGGTTTCACCGTG[G/T]TAGCCAGGATGGTCT | 5336 |
| rs544025120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861426 | ACATGCCCGATGGGA[G/T]GATTTGGAACTATTA | 5336 |
| rs544034858 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919995 | GTCTAGGAAGATCTC[A/T]CTGAAAAGGAATGAG | 5336 |
| rs544052083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885577 | AACCCCAGACTTTGC[A/G]TCATTTTGTTTGTAA | 5336 |
| rs544052844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810663 | TTATTTTTTGCTGGT[A/G]ATGTTGCTCTTTAAA | 5336 |
| rs544061628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840995 | TTAAAACTCTTATCT[A/G]TTGAATAGTTCTGCA | 5336 |
| rs544064683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800882 | TCACAAAGGTCCTTG[C/T]AGGAGGGAGGCAGGA | 5336 |
| rs544093313 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815158 | GCACCTGTGATATGA[C/T]GCTCTGGAACGCCTC | 5336 |
| rs544101199 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81786758 | AAAGTTTCTAAGACT[A/G]TTTTTAACAAATAGA | 5336 |
| rs544112188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865616 | CCTGGACATGGGATG[A/G]TTCCTTTGCCCTGCT | 5336 |
| rs544129296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816246 | TGTGGCAGCACATGC[C/G]TGTAATCCCAGCTAC | 5336 |
| rs544131336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812114 | GACTGCAGTGGCGCT[A/G]TCTCAGCTCACTGCA | 5336 |
| rs544136071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887148 | CTTTTGAGATGGAGT[C/G]TCGCTCTGTCACACA | 5336 |
| rs544143851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791647 | TCGGCTCACTGCAAC[C/G]TTTGCCTCCTGGGTT | 5336 |
| rs544146154 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861639 | ATTTGGTACACACTG[G/T]TCTCTTTCAGCCTCG | 5336 |
| rs544150627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867036 | GCCGTGGGTGCTGTC[C/T]CTGTGGTACCAGTAA | 5336 |
| rs544169768 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941330 | ACTCCAGCCTGGGTG[A/T]CAGAGCAAGACTCAG | 5336 |
| rs544179358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890585 | TGAACCATTGCAAGC[A/G]CAGAAACAGAATGCG | 5336 |
| rs544182316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942858 | GATCTTACTTTAAAA[A/G]GTGTCTGTATTTCCC | 5336 |
| rs544184506 | snp | A/T | 1.83179e-05 | 0.00302632 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870944 | AAAATCGGTAAGATG[A/T]TTCTTGAGCAAGTGA | 5336 |
| rs544190437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817645 | ATTATTTTATTTTAT[C/G]TATTTATTTTTAAAA | 5336 |
| rs544209630 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946757 | GAGTACCTTTTTCCT[A/C]CTTTACGCCAGAATT | 5336 |
| rs544221577 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845576 | CTGCTCCTCATGACT[G/T]GGATAGCTCCTGGGA | 5336 |
| rs544227087 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790006 | CTTCCAGTGCCCTTG[A/G]ATGAGCTTTGCTGTG | 5336 |
| rs544233504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927233 | TCTGCAGGTCCAGTT[A/T]TTCAGGGAGCTGTGC | 5336 |
| rs544250802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874795 | GAGTTTCCAAAAGTT[C/T]GGCAGCAGCAGGAGG | 5336 |
| rs544261654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795338 | GTGATGTTTGAGCTG[A/C]GACTTGAAGGGTGAG | 5336 |
| rs544264356 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81791983 | ACATCACTTGCACCA[A/C]CTCAGATCAGCAAGC | 5336 |
| rs544283760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821236 | GTGGGGATTCAGTGA[A/G]TTAACATGTGAGTGA | 5336 |
| rs544287594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877793 | CGCTCCTTGGCTTGT[A/G]GATGTCATTGCATCG | 5336 |
| rs544297739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902744 | GCTCATAAAGACATA[C/T]CCAAGACTGGGTAAT | 5336 |
| rs544306218 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837792 | AATGATACAGAGAGA[A/T]CTCATGTGAACGTTA | 5336 |
| rs544320061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950928 | GAGATAGAAACCAAC[C/T]GAATAAAACACAAAT | 5336 |
| rs544322048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799080 | CGCCAGTTTCCTGTT[G/T]AGACAGCTCTGAGCT | 5336 |
| rs544352257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943783 | ACATTGTAGCGATAG[A/G]GAAAAATAGGTCAGA | 5336 |
| rs544354331 | snp | A/C/G | 0.00319034 | 0.0398225 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868012 | TGGCCCTCGCTTCCC[A/C/G]CTTCAGCTGAACCTC | 5336 |
| rs544363212 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841091 | CACATGGAAGCAGGA[C/G]ACTGATTTTCGCCTC | 5336 |
| rs544388398 | in-del | -/TTG | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910091 | GCCCTGCATCTGGTT[-/TTG]TTGTTGTTGTTGTTG | 5336 |
| rs544389264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939289 | CCAGAGGATCAGCCT[A/G]ACCTGGGAGATCTTA | 5336 |
| rs544400529 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827966 | ATGGTGGCGGATGCC[G/T]GTAATCCCAGCTCTT | 5336 |
| rs544404030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807163 | CTTATCTTGTTGAAC[A/G]TGGTGATTCATGTGG | 5336 |
| rs544407829 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962999 | CCCTGTATTTCTCAG[C/G]TGAGTGATAGGCTCC | 5336 |
| rs544411850 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783119 | CTGGTCCCTTGTCCT[C/G]GTTTCTGTCTAATTG | 5336 |
| rs544418433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833288 | TAGAGTCACTGGGCT[C/T]TGGAGAAGCTTCTGG | 5336 |
| rs544419063 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959588 | TGTTATCTGGTGCTA[C/T]CACTCCAGTTACTCC | 5336 |
| rs544434353 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829131 | TTATTTTTTTTGAGA[C/T]GGAGTCTGGCTCTGT | 5336 |
| rs544435013 | snp | A/G | 6.72111e-05 | 0.00579664 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919667 | GCGCTACAATATGGT[A/G]GGTGGTGGACTCCCT | 5336 |
| rs544438213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883683 | TGCACCTTTTCTGGC[C/T]ATCATCTCAGGTGTC | 5336 |
| rs544443864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810410 | ATTTGCAGCATCAGT[A/G]TTGGTGAATTTGCCT | 5336 |
| rs544487680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871393 | GCCCAGGCTGGAGTG[C/T]AGTGGTGTGATCTTG | 5336 |
| rs544497665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938982 | CTTTGTGGGAGTGCT[C/T]TTCGTGGGGGATTTT | 5336 |
| rs544504918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818448 | GCATGATGACTAGCA[C/T]ATACCAGGTAGACCA | 5336 |
| rs544507217 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889964 | TGGCGGAGGCTAGGG[-/T]TTTTTTTTTAAAGAT | 5336 |
| rs544517986 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888078 | CTTAGGATCATGAGG[A/T]ATTGTTCCTGGGCCT | 5336 |
| rs544519834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813788 | GTTCTGTGGCTAGTT[G/T]GGGCTTCCTTACAGC | 5336 |
| rs544526708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927605 | TTTGCAAACCTGGTG[A/G]TTGTTCCCTCGCCGC | 5336 |
| rs544542242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840699 | CAGGCAGTAATGTTC[G/T]CTAGACCCCTGCTCA | 5336 |
| rs544566154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822625 | AACTGGGCATGGTGG[C/T]GTGTACCTGTAATCC | 5336 |
| rs544573243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826352 | TGATCTGTGTCCTCA[C/T]CTAGGTGCAGTAGGA | 5336 |
| rs544579909 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848169 | AAGAGCGCAGAAATA[A/G]ACCCACACAAATATC | 5336 |
| rs544582942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951899 | TATTGTATACAAATT[C/T]AAACTGTACAAATTC | 5336 |
| rs544583119 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803775 | CATCCTCTACCTCCT[A/G]GATTCAAGTGATTCT | 5336 |
| rs544604745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952387 | CCAGTCATTGGATTC[A/T]CAATTCCAGATATTG | 5336 |
| rs544606063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956612 | CCATGCTCCCTTTGG[A/G]CATGCTTGTGAGATG | 5336 |
| rs544618163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956154 | ATGGCATCGTGTGAT[G/T]TGTGATCTTTTAGAG | 5336 |
| rs544620463 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841022 | TGCATGAATATGAAG[C/G/T]ATTAGAATCACAGAC | 5336 |
| rs544628898 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827551 | TCAGAAACATAAATA[C/T]CTGCAGGCAGCTGGA | 5336 |
| rs544647973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943465 | CAAGTGGGAAGTCCA[C/T]CCCCATTATCCAGTC | 5336 |
| rs544671673 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891077 | TTGAGGCAGGAGAAT[C/T]GCTTCAACCCAGGAG | 5336 |
| rs544672815 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833617 | TCACTGTACCTTCCA[A/C/G]CTCCTAGGATCAAGA | 5336 |
| rs544693836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829269 | ACACACCAACGTGCC[C/T]GGCTAATTTTTGTAT | 5336 |
| rs544695517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930632 | GTGCACCTGTGGTCT[C/T]AGCTACTAGGGAGGC | 5336 |
| rs544712192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880633 | TACCATTAAATGAAT[A/G]TCCCTAAAACAAATT | 5336 |
| rs544729691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844804 | TACACATGGCCATGT[A/T]TGTGTGTACACACAT | 5336 |
| rs544743222 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857802 | TGGCTGCTATGAGCT[A/G/T]TGTGGCCTTGGACAC | 5336 |
| rs544746011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779918 | AGACTTTTGGAGAGC[C/T]TGCAGGACACTCGCG | 5336 |
| rs544754565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818667 | TTTTCTCTGCAGCAG[C/G]AAGCCTTGTTGGCAC | 5336 |
| rs544754997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883954 | GAGACGACATGGGTG[C/T]GTGTCACAGCGGGAG | 5336 |
| rs544756657 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855286 | GATCTGAAGGAACTG[A/T]CCTGAGATCTTCTGT | 5336 |
| rs544792912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796988 | ATTCAGCCACTGATA[C/T]TATGGATGGGTTGTG | 5336 |
| rs544802746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906867 | ACATGGCGAATCCCC[A/G]TCTCTATTAAAACTA | 5336 |
| rs544804418 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902834 | TCATGTCAGAAGGCA[A/G]AGGAGGAGCAAAGTC | 5336 |
| rs544807381 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842918 | CTGGAGTGGGGTGCC[A/G]GCCTTTGAGGCTGAC | 5336 |
| rs544808000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841496 | TCTGCCCACTTCGGC[A/C]TCCCAAGGTGCTGGG | 5336 |
| rs544816170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848430 | AGGGCTGCTTGTATC[A/G]TTAGAATGGCTGTTA | 5336 |
| rs544838690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829538 | CTCTGTTTTATATTG[C/T]CATGATACCTTTGCC | 5336 |
| rs544855351 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960173 | GGTTCTTTCCTCCTG[A/T]CCTTGACAGAGTAAC | 5336 |
| rs544860193 | snp | A/G | 1.65655e-05 | 0.00287793 | missense | PLCG2 | GRCh38.p7 | 16:81891502 | TTTTCACGAGAAAAC[A/G]GCATCTGGGATGAGA | 5336 |
| rs544862304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779884 | GGAGCGATACCGCGG[C/G]AGGCGCAGTCCTTCC | 5336 |
| rs544862385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849342 | ATTCCAGAGCAATTT[C/T]AGAAGTAGAATTGTT | 5336 |
| rs544865421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855975 | CACCTGCAGGCTGAG[C/T]CCTGACCCCCTGTTC | 5336 |
| rs544868025 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841842 | TGAAGTAACCTAACA[A/C]CTTTGGTTTTTCTTA | 5336 |
| rs544879129 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81922728 | TTTGGGTGGGAGGAG[A/T]AGGAAGCTGCTCATT | 5336 |
| rs544887784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783663 | ATAAATGAGACGAAC[C/G]AGACACAACAGGTGC | 5336 |
| rs544888153 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837428 | ATCAGGAGGCTGCAT[A/G]AACATCTATTTCTAG | 5336 |
| rs544889842 | snp | A/G | | | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81869292 | GTTCCTTAAAGATAA[A/G]TTTGTGGTAAGTTTC | 5336 |
| rs544894722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845497 | ACTGTCCAAAGCTAT[A/C]TGCTATAAGCTGGGG | 5336 |
| rs544897612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833725 | TTTTTTGTAGAGGTG[A/G]GAACTTACAGCCAAG | 5336 |
| rs544903110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859641 | CTGGGTTCATGCCAT[G/T]CTCCTGCCTCAGCCT | 5336 |
| rs544930004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883998 | TCTAGCAGGTCAACA[C/G]CAGGGATGTTCCTAA | 5336 |
| rs544948246 | snp | A/G | 3.38564e-05 | 0.00411425 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910760 | AGGCAGGCGGTGGTC[A/G]GGTTAGCTCCACCAG | 5336 |
| rs544949260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837028 | CAGCGTTCTCCATGG[C/G]AAGACTCAACATCAG | 5336 |
| rs544952510 | in-del | -/AA | 0.492287 | 0.0616198 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792480 | GCAAGGCTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 5336 |
| rs544969343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887175 | CACAGGCTGGAGTAC[A/G]GTGGCGCGATCTCTG | 5336 |
| rs544972231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863314 | TATTTGTCCTTTTGT[A/G]TCTGGCTTATTTCAC | 5336 |
| rs544972357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867724 | ATTTTTGGAGATGGA[C/G]TCTTGCTCTGTCACC | 5336 |
| rs544980126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919927 | AAAAACACTGGGCAG[A/G]TGGATAAGAGGATAC | 5336 |
| rs544983760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849374 | AAATCTGGCTATTGC[C/T]GGAAGACAATGTTAC | 5336 |
| rs544988551 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814353 | GGTCAGAATGTTTAG[A/C/G]AGTGGAGGATCTGCG | 5336 |
| rs544993340 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956094 | CCGGTGACCTTTAAC[C/G]TACTTTGTCTCTGTG | 5336 |
| rs545023745 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907041 | GACTCTGTCTCAAAA[A/C]AAAAAAAAAAAAAAC | 5336 |
| rs545039146 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858421 | TGCTGCCTTTAGCCA[A/G]CATGGGCTACAGGGG | 5336 |
| rs545059046 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800494 | TCCCGTGTTAGTTTG[C/G]TGAGGATGATGGCTT | 5336 |
| rs545065394 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849096 | AGATGCTTAGGCCAC[A/G]TGGGGTTGGAGGGGT | 5336 |
| rs545067452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852788 | GAGCTTGTCTGTGTT[C/T]CACATGTTGTCAGCT | 5336 |
| rs545069921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919306 | CTAGATCTGTTTTGA[A/C]AATACCCACATCATT | 5336 |
| rs545083611 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918910 | TTTCTTTTTTTTTTT[A/T]AAAAAAGTCACTGTT | 5336 |
| rs545091358 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926971 | CTGGTCACTTGGCCA[C/G]TTGCTGTCTGTCCCC | 5336 |
| rs545096791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817698 | ACTGTGTTGCCCAGG[C/T]TGGTCTAAAACTCCC | 5336 |
| rs545100711 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942059 | TTTGGTACACCTTTA[C/T]GTTCCTAGCCTTGAC | 5336 |
| rs545137995 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947200 | ATTTAAAAGAAAATT[C/G]TGTTGATGCAGATTT | 5336 |
| rs545144889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923102 | CAGTCTTGGCTTAAT[C/T]TAAAAGGCATGTCCT | 5336 |
| rs545161330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799872 | TGCTGGGATTACAGG[C/T]GTGAACCACTGAGCC | 5336 |
| rs545162924 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81912429 | TCTTTTCACAAATTC[C/T]CTTTGCTGAGGTGCC | 5336 |
| rs545190491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803970 | ACAGGTATGAGCCAC[C/T]GTGCCTGGACTCTTT | 5336 |
| rs545190697 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931346 | GTGATGTGTACTTAC[C/T]CCGATGGAAAGTAGA | 5336 |
| rs545194240 | snp | A/G | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777966 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 5336 |
| rs545205432 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959896 | TCCTCACTTCATTCT[A/T]CTTTAAAGCCACAGT | 5336 |
| rs545206264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807478 | TCAAGCCCCCACATC[A/G]TCATCATTGTCATCA | 5336 |
| rs545245843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940193 | CCGATTGGGTGGCTT[A/G]GAGAGCAGGTGTACA | 5336 |
| rs545246628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864505 | TCTCAGATCTCACAC[A/T]AACTCATTGTGTGAA | 5336 |
| rs545251321 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780291 | TCCCCCTCTGGATAC[A/T]GGAGCCACCCAATTT | 5336 |
| rs545254533 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859285 | ACTGCGTCCATTGTG[A/C]TCTGCGGATGCCATG | 5336 |
| rs545270539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788284 | GCTGAAGGATATGGC[A/C]TATATATATTTTAAT | 5336 |
| rs545271002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793057 | TTAATACAATAAGAC[C/T]AGAAAGAAAAAAGGC | 5336 |
| rs545272895 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833339 | CAATCTGTCCACACC[A/C]CCAGGGTCCTTTTTC | 5336 |
| rs545276382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915944 | CAGTAGAGAGGTCCT[A/G]GTAGAAAGCACAGTT | 5336 |
| rs545283331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868041 | TCACTATGTGGCTTC[A/G]AAGAAACACTCATGC | 5336 |
| rs545284388 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788847 | TTGGCCGGCTCCACC[C/G]CCAGGTGGCCCAGAA | 5336 |
| rs545293417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814735 | GGGACATGAAGCACA[C/G]GCAGAATGGAGAGCA | 5336 |
| rs545303231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859342 | AATCCTCCTCCTGGA[A/G]GGAGCCTCTATTCCG | 5336 |
| rs545313919 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857569 | ACTTGCAGACAGCTG[A/C]CTTCTTGCCATGTGC | 5336 |
| rs545329310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939366 | AAAAGCCAGGAGGGA[A/T]CCGTGATTGGTGGGC | 5336 |
| rs545330392 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883720 | TGGGAAGCCTTCCTT[G/T]ACTGATGGGAGGATG | 5336 |
| rs545333894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811818 | TCTTGTGAATAGTGC[C/T]GCAATAAACATATGT | 5336 |
| rs545354379 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947107 | GGCCCGCTGCTCTGC[A/G]AGGCTGTTGTAAACA | 5336 |
| rs545380414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952956 | TAATCAGATGATCAA[C/T]GTTACCAACCACCTG | 5336 |
| rs545390496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823085 | AGCCGTAGGGCACTT[A/G]TAAAGCAGGCGAGGC | 5336 |
| rs545412590 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886250 | TGCTGGGCTGCCCTT[A/G]GAGATCAGGGATCTG | 5336 |
| rs545416394 | in-del | -/CCTGTGCTCACCTGGTCA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883417 | CTCACCCTTCTGCCG[-/CCTGTGCTCACCTGGTCA]CCTGTGCTCACCTGG | 5336 |
| rs545421919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784459 | CAGAAGGCTGAGCCC[A/G]GCTGGAAGCACAGAC | 5336 |
| rs545439838 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952481 | ATGGGATAAATAAAA[C/T]ATAAAAAGGACCTGG | 5336 |
| rs545442995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804432 | GGTGCTGACTAGGGC[A/G]TAAATGAATGAGGCA | 5336 |
| rs545454609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802138 | TTTTTTTTTGAGACG[A/G]ATCTCGCTCTTTCGC | 5336 |
| rs545456597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854328 | GCAGAGATAGCTTTG[C/T]GGGATCCTGTTGGGG | 5336 |
| rs545482902 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873679 | TCACGCCTGTAATCC[C/T]ACCACTTTGGGAGGC | 5336 |
| rs545494464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853955 | TTAGTGCCTTCATTT[C/T]CTCTTCCCCCTTTAA | 5336 |
| rs545540771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805633 | ACACCCCCTTCCCCC[A/G]CCCCACTCACAATGC | 5336 |
| rs545545669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866607 | AGCTCCACTGGGGCA[C/G]TAGCATGAGAGGATG | 5336 |
| rs545548992 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867203 | CGCGCTACTTCCTTC[C/T]GCATGCCACAGCAGA | 5336 |
| rs545577952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876269 | CTCAAGTGATCCACC[C/T]GCCTTGGCCTCCCAT | 5336 |
| rs545594986 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888460 | TCAAACTCCTGAGCT[C/T]AGGCAGTCCACCCGC | 5336 |
| rs545596361 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944213 | TACATAAATAAGATG[C/G]ATTGATGGGTAGATA | 5336 |
| rs545617454 | in-del | -/TGTT | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850397 | CGAAAAGGATCTTTC[-/TGTT]TGTTTGTTTTTGAGG | 5336 |
| rs545625892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837952 | TGTGTGTATTTAGTT[A/G]TGTACAATTTGGTCA | 5336 |
| rs545636741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846195 | TAGGAGGTTGTAGTG[A/G]CTGTAAGCCAAGCCA | 5336 |
| rs545638529 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797202 | GTTCCTGACAAGTCA[G/T]TGCAGGTCCAACGTC | 5336 |
| rs545641582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870134 | TAATAGAAAAAGAGA[A/T]AAGGGTAGGTCAGAA | 5336 |
| rs545643352 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850705 | TTAAGCATGTAGAAG[C/T]GGGGAACTTCTGGCA | 5336 |
| rs545650785 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915399 | GTTGAGTTGTTGCCC[G/T]GCTGTGATTGGTGGA | 5336 |
| rs545659130 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882273 | CCTGCTGGCCAAGGC[A/G]GGAGTCCTGCCTTTA | 5336 |
| rs545661666 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850703 | ATTTAAGCATGTAGA[A/C]GCGGGGAACTTCTGG | 5336 |
| rs545688019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795236 | ATAGACGCTAGGAAG[A/G]AAAGGAACAGGGTAC | 5336 |
| rs545691356 | in-del | -/CCT | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856348 | AGTAGGGTTAAGTAA[-/CCT]CCTGAATGTTACACA | 5336 |
| rs545719650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891800 | TAATAATAATCTCTT[C/T]TCTGTGGCCCTAAAA | 5336 |
| rs545732934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847511 | ATCCTGAGGTATCTA[A/G]GAGCCCCCAGCCCTA | 5336 |
| rs545742714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897914 | TGTTGCTGTGAGACA[A/G]TGAAATTATGGACGT | 5336 |
| rs545751935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952171 | AAAAAACAAAACACC[A/G]TGTGAACAAGTAGAA | 5336 |
| rs545752272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828557 | AGCGTCATTTTTATT[C/T]TGTGCTGTGGTGTGG | 5336 |
| rs545763901 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873856 | TCATTGATGGTTTCC[A/T]CTGTGGTAACATTCC | 5336 |
| rs545770284 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827105 | CCTTGTTGACCTTGC[A/G]CTGAAATAAGACTCA | 5336 |
| rs545778939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950045 | AAAAAGGAGATCAAC[A/G]TAAACTTGACCAAGA | 5336 |
| rs545823310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898285 | GGCAGCAAAAGCCAT[C/G]CTTATTGGTATTAAG | 5336 |
| rs545827366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945876 | CACAGCTGCAATCAC[C/T]ACACTCAATGTGGAA | 5336 |
| rs545838544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809997 | GGTTCTCTCCTTTTT[C/T]TTTTCTTTTTTTTGA | 5336 |
| rs545875834 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929172 | TGTCCAGTGGTGGCC[A/C]GGGTCTGATGTGTGC | 5336 |
| rs545878545 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954215 | TTTTATAGTAACAGG[A/G]TCCCGCTATGTTGCC | 5336 |
| rs545887414 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933804 | GATAGAATTTGGGGA[G/T]GCCCAACAGGGTTGC | 5336 |
| rs545887680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938561 | GCTCAGGTGAGTTTT[A/G]CCTGTTGAGTCAGGT | 5336 |
| rs545893012 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827886 | ACCTGAGGTCGGGAG[A/T]TCAAGTCCAACCTGA | 5336 |
| rs545913298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879402 | GTACTTCTCAGTTTG[C/T]CTAAAAAGGCTAAGT | 5336 |
| rs545922788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831501 | GGCCCTCTCTATTTG[C/T]CTCAGTTTTACACCT | 5336 |
| rs545931526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886652 | GTTAAAAGTATGTTT[A/C]TAGAATCAGTGTTTC | 5336 |
| rs545933255 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801295 | CCTCCCTAGAGAAAT[C/T]AGTATCATGATTTAA | 5336 |
| rs545945847 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913894 | TGGGGACCGTGGTGA[C/T]GGTCATTATCACTAT | 5336 |
| rs545954406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882610 | TGCTCTGCAATCCCT[C/T]CCTCTGGCCTGCGTT | 5336 |
| rs545959876 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886454 | TGCAATGAAAAGAAA[G/T]CTTTACAACTCGATT | 5336 |
| rs545970600 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860842 | CAGGCATGGTAGCAC[A/G]CTCCTGTAGTCCCAG | 5336 |
| rs545977792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894650 | GGTCGAGGTGGGCGG[A/T]TCACTTGAGATCAGG | 5336 |
| rs545985490 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777802 | GGGTGGATCACTTGA[A/G]GTCAGGAGTTTGAGA | 5336 |
| rs545985626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790818 | CAAAGTCTGGAGACG[A/T]GTTGATTTTCTCACC | 5336 |
| rs545990537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942697 | GAGCACTTTGAGGCC[A/G]AGAGACTATGACTTA | 5336 |
| rs545994933 | in-del | -/AGGCATGAG | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910366 | AAGTGCTGGGATTAC[-/AGGCATGAG]AGGCATGAGCCACTG | 5336 |
| rs546000375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864353 | AAAACAAAATGAAAT[A/G]AAATACTTAGCTCCT | 5336 |
| rs546006730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950998 | TCAAAAAGGCCAAAT[G/T]TTGTTTTGAGACAGT | 5336 |
| rs546010088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816854 | AAGCAAGAACTGAAA[A/G]TGCGGTTGCGCTGTT | 5336 |
| rs546027398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791351 | TTAGCAGGGATGGCT[G/T]CCCTGATCCTGTGGG | 5336 |
| rs546031906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839986 | CCCTTGAGCCTACGA[A/G]TTCAAGGATGCAGTG | 5336 |
| rs546034064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844043 | GTGCAGTGGTGTGAC[A/G]TCGGCTCACTACAAG | 5336 |
| rs546050714 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930015 | ACTTTCCACATGTGA[C/T]TTTCTCTTAATGAGC | 5336 |
| rs546054208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874507 | AGGTAAATGCCCATC[C/T]CCTAACCTGTTAGCA | 5336 |
| rs546063460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946324 | TGGTGAGGGTAGAAA[C/T]GGCCCGTGAATACAA | 5336 |
| rs546071532 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931016 | CCAAAAAGATATTCA[G/T]TGTTTCTTTTGATCA | 5336 |
| rs546072322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843623 | TTTGATGAACCCATT[G/T]CTAAGCATGTTTGCA | 5336 |
| rs546077945 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877312 | ACAAAAAAAATTAGC[C/T]GGGCATAGTGGCGGG | 5336 |
| rs546079660 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899380 | ATTTATACATACACG[A/T]TCACATGATATAGAA | 5336 |
| rs546086271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828906 | GGAGATAAGAGGCTG[A/T]ATCTTACCAACTGCA | 5336 |
| rs546116777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880098 | GAAAAAATATTAGCC[A/G]GGCATGGTGGCGCAT | 5336 |
| rs546121169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955384 | ATCGGGAAAGGCCAA[C/T]TGACTTGACCCTCCT | 5336 |
| rs546138257 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803089 | TCTGGACATTTCTCA[A/C]AATACATGGCTTTTT | 5336 |
| rs546160382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866185 | GGCCTCTCCCTTGCT[C/G]CCAGGATGAGCTCCA | 5336 |
| rs546163257 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806225 | TTGGATAGCACAGAT[A/C]TAGATTATACCTCTT | 5336 |
| rs546173146 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930476 | CATTTAGCTGGGTGT[A/C/G]GTGGCTCATTCCTGT | 5336 |
| rs546175643 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959137 | AAGGGAGGTGGTTGG[C/T]AGAGTCACAACTTCT | 5336 |
| rs546193612 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933333 | AAGGAAGAAGGCCCC[A/G]TCCCACTCTTGGGAA | 5336 |
| rs546195713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919027 | AATATTTTAGGTTTT[G/T]CAGGCCATATGGTCT | 5336 |
| rs546197216 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865788 | CCTCTCCCTTGCTCC[C/T]AGGATGGGCTCCACT | 5336 |
| rs546201988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832281 | TCTCTCCTGGGCTCC[A/G]CTCCACATGGCAGCC | 5336 |
| rs546202688 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845056 | CCCTCAACTTCTTGA[A/G]TAGCTGAGACTACCA | 5336 |
| rs546204341 | snp | A/G | 9.93706e-05 | 0.00704808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858387 | CTGTTGATTTGCGTA[A/G]TTGCTGATTCCTTTA | 5336 |
| rs546228674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917510 | AATTTACAGTCCCAC[C/T]CACCAGGTGCAGGGG | 5336 |
| rs546229583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853179 | CTACTAAAAATACAA[A/C]AACTAGCCGGGCATG | 5336 |
| rs546232574 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883008 | GACTCTGGGGTGCAC[C/G]AGAGCTATTTTGGAG | 5336 |
| rs546243838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836447 | TGGTAGTGGTTAAGA[G/T]TGCAAGCTTTGGGCC | 5336 |
| rs546272502 | snp | A/C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81957165 | TTAGCTGGGCATGGT[A/C/T]GTGGGCGCCTGTAAT | 5336 |
| rs546278368 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830770 | AGAGGACCCTGGAGG[A/T]GACTGACAGACACAG | 5336 |
| rs546282925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869797 | TTTGTTGTGTAATCA[A/C]GTTATTGGTGGGTCT | 5336 |
| rs546283767 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81902693 | GGACTCTACCCTCAT[C/G]ACCTAATCACCTTCT | 5336 |
| rs546317629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912826 | GCAGTGCCCTGCCCC[C/G]CCAGCATCAGCGACA | 5336 |
| rs546318327 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887800 | TGTCATATTTCATCC[A/C]CTTTTCCTATGAATA | 5336 |
| rs546320033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886327 | TTAGGACCCGAGCAG[C/T]CATGAGCATCCATGC | 5336 |
| rs546330284 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875548 | CCCCCATGTATCATC[A/C]GCTGACTTCAGCCAT | 5336 |
| rs546336250 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801946 | TCAGCCTCCCAAAGT[A/G]TTGGGATTACAGGCA | 5336 |
| rs546349103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821728 | CGCAGAGCCCCAAAA[C/T]AGATCTTTCTCCGCT | 5336 |
| rs546352668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893873 | TCCATGTTTTCTTTC[A/G]AATTGTAAAAAGGTT | 5336 |
| rs546365910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805942 | ACTGTACGCAGTCAT[C/G]TGTGTAGTTTAAAGT | 5336 |
| rs546366286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786323 | AAAATGAAAGCATTG[A/C]CAGTTTGTGTGGATC | 5336 |
| rs546368781 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950031 | AGAAATAAGGAGGAA[A/G]AAAGGAGATCAACAT | 5336 |
| rs546371204 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802355 | CTGACCTCGTGATCC[A/T]CCCGCCTCGGCCTCC | 5336 |
| rs546382557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870681 | TGTTAAATAGCATGA[C/T]TTTTTCCTTTCAAAA | 5336 |
| rs546394885 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808257 | TTCCAACGGGGCTAC[A/G]CTGTTTTGCATTTGC | 5336 |
| rs546396937 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962040 | CACCGCTCCATGTGC[C/G]TCCCTCCCGAAGCTG | 5336 |
| rs546399897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898912 | AATATAGGCTGGGCA[C/T]AGTGGCTCACGCCTG | 5336 |
| rs546413408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799679 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCACA | 5336 |
| rs546456508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883044 | AAATGTAGACACCAG[A/G]GCCTGCCCCTTGAGA | 5336 |
| rs546462384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922815 | TGTTCATTTATGCCC[A/G]CCAGGCAGAAAGCAT | 5336 |
| rs546478989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909497 | GTCTCAGTCACTGCA[A/G]CCTCAAACTCCTGGG | 5336 |
| rs546491219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782409 | CTTTTTTTGAAAAAA[A/C]CAAAAAAAGCAGAAG | 5336 |
| rs546495955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929956 | GTAGAAATCTTGGAG[A/T]CAGGTTTGAACTGAG | 5336 |
| rs546495970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802656 | AGCTCACTACAACCT[C/G]TGCCTCCCAGGTTCA | 5336 |
| rs546518116 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958687 | TTTAAAAAGCCCATC[A/T]GAGAGACCAGAGCCG | 5336 |
| rs546529282 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790913 | GTGCACAGGACAGTC[C/T]GCACCACAGAGAGTG | 5336 |
| rs546531752 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824909 | ACCCAGGTAGGCCCA[A/G]TGTAATTACAAGGAT | 5336 |
| rs546548972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812647 | TTGCCTGCTCACTCT[G/T]ATGATAGTTTCTTTT | 5336 |
| rs546551315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913144 | CTGCAGCTGCTGCCC[A/G]ACCACCTCTAGGCCT | 5336 |
| rs546567711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839748 | ACCAAGTTTAAATGG[C/T]ACCAAAATGATGAAC | 5336 |
| rs546580205 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828847 | CCCTTAACTTGCATT[-/C]CTTTTTCTTTTCTGA | 5336 |
| rs546587616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813094 | CTTGTAGTATAGTTT[C/G]AAGTCAGGTAGCATG | 5336 |
| rs546602248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874287 | TTGACCCAGCCCCAT[A/G]CAGCTCTGTCTGCTC | 5336 |
| rs546604566 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81938792 | CAATGCTTCCCTTTG[G/T]TGTCCCAGGTTCTCG | 5336 |
| rs546605518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889646 | GTTTTTTTATGTTTT[A/T]GTTTGTTTGCTTGTG | 5336 |
| rs546607048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874014 | TGCCCTAGATTGCCC[C/G]GTGTGGAACTTTGTA | 5336 |
| rs546608155 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840043 | GCCTGGGTGACAGGG[C/G]ATGACCTTGTCTCCA | 5336 |
| rs546611680 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801664 | TTTTCGATATTAGAT[A/G]GTTGTTTTTTATTTT | 5336 |
| rs546634162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945923 | ATTTCTTCTGAGTGA[A/G]TCATTTTTATTTCTA | 5336 |
| rs546642068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814201 | GGAATGGTACCGGGT[A/C]TGAAGGATAGGCTGT | 5336 |
| rs546643838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877220 | AGCACTTTGGGAGGC[C/T]AAGGCGGGCGGATCG | 5336 |
| rs546645134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843327 | TTGGTACCCTTTCTC[A/G]CACCTTTACACTCAT | 5336 |
| rs546648704 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841882 | CCTTGGCTGAGATCA[G/T]TAAGCAACGCTGGGG | 5336 |
| rs546663232 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934251 | TGTCGAGAATTTTCA[C/T]AGTGAGAGGAAGAAA | 5336 |
| rs546671304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951018 | TTTGAGACAGTGTTT[C/T]TTTCTGTCACCCAGC | 5336 |
| rs546681360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955462 | AGGCAAAACATCCTC[A/T]TCCTCCCCCTGCATT | 5336 |
| rs546686163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893500 | TCACTTCCTGCGATT[G/T]TGGCCTGACTTCAGA | 5336 |
| rs546717734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820418 | TAAACATGGAATGAA[A/G]CAGTAGACTGTGTTT | 5336 |
| rs546724071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814537 | ATCTCTACTAAAACA[A/G]TACGAAAATTAGCCA | 5336 |
| rs546733190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802737 | CCACCACGCCCAGCT[A/G]ATTTTGTATTTTTAG | 5336 |
| rs546747866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945613 | CAACTTGCCCCCCTC[A/G]GCCCCAAATAAAAAG | 5336 |
| rs546763067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828650 | GGGTCTTGAGAAAAG[A/G]TTGCTTTTACAACCT | 5336 |
| rs546766495 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778126 | CATGCCTGTGATCCC[A/G]GTGCTTTGGGAGGTA | 5336 |
| rs546770746 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802703 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGGCAT | 5336 |
| rs546795062 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958958 | GCTAAGCATTAGGGT[A/G]TTACAGAAAATTTCA | 5336 |
| rs546805961 | snp | A/C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789280 | ATTTCACTCGCTTAC[A/C/G]CGGATGCGCTCTCTC | 5336 |
| rs546809139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901687 | CGGGCTCTGTCACCA[C/G]CAGAAGTCATGAGTG | 5336 |
| rs546818050 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858111 | GTCCTAGGGCCATGA[C/T]GGTGTGAAAGGGGAT | 5336 |
| rs546821765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904663 | GGTGGTGTTGTTGTT[C/T]ATTCACCGAGTATCA | 5336 |
| rs546825194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817744 | CCATGCCCTTGGCCT[C/G]TCAGAGAGCTGGGGT | 5336 |
| rs546826841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807616 | TGTATGTGTTCAATA[A/C]GCATTATTTCCATTT | 5336 |
| rs546834100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882755 | CCTCATTCTTGCTCA[C/T]CCCACCTCATTCTGG | 5336 |
| rs546842368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909086 | ATCCATGTCTCAGTG[C/T]ATTAAAAGATACTTC | 5336 |
| rs546846536 | in-del | -/GAGT | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778353 | CCAGCCTGGGTGACA[-/GAGT]GAGACCCTGCCTCTT | 5336 |
| rs546847553 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805889 | AAGTGATCCTCCCAG[C/G]TCAGCCTCCTGAGTA | 5336 |
| rs546850221 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962120 | TCGGTCAAGGGTATA[C/T]GAGTAGCTGCGCTCC | 5336 |
| rs546853295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813966 | AAGTTTGTGGCTATC[A/G]TGAATCCACCAGAGA | 5336 |
| rs546861649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840747 | CGATTCCTAACGGGC[C/T]ACAGACAGGTGCCAG | 5336 |
| rs546862055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890690 | GGAGCGACTGACCCA[A/T]ATGAGGTCGTTCTCA | 5336 |
| rs546865559 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830445 | CCAAGTAGCTGGGAT[G/T]ATAGGCGCATGCCAC | 5336 |
| rs546884678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836014 | ATTTCCAAAGAAGGC[C/G]ACATTCACACATACC | 5336 |
| rs546888291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821786 | CAAATGCTTTGCATA[A/G]CTTCCTACCCAAAAG | 5336 |
| rs546893165 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782048 | GGCTAATTGTTTTGT[A/T]TTTTTTTTTAGTAGA | 5336 |
| rs546912147 | snp | C/G | 1.65847e-05 | 0.0028796 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937885 | CCAGAGGAAGATCCT[C/G]ATGACGCTGACAGTC | 5336 |
| rs546920974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874234 | TCTGGCTATAAATAG[A/G]GTCACATCTCGCCAT | 5336 |
| rs546942391 | in-del | -/TT | 0.380138 | 0.213458 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823692 | ACCATGCCCAGCTAA[-/TT]TTTTTTTTTTTTTTC | 5336 |
| rs546949364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844587 | TAGGCCTCCCAAATC[A/G]CTGGGATTACCGGCG | 5336 |
| rs546951753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823212 | TTTCAGTTCAGCCTA[A/G]GGGAGGTCTGGCTTC | 5336 |
| rs546964519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886042 | ATTCATGCACTTTTT[C/T]CCCTTCATTATTTTC | 5336 |
| rs546968550 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898953 | ACTTTCGGAGGCTGA[C/G]GCGGGTGGATCAACT | 5336 |
| rs546983455 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842935 | CCTTTGAGGCTGACT[C/T]TAGGAGACTCAGTGT | 5336 |
| rs546984792 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807260 | AGGTCAGCTCTGGGA[C/T]CCAAGAAAGGGCAGG | 5336 |
| rs546988293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894820 | AGAGGTTGCAGTAAG[C/G]TGAGATCGCGCCGCT | 5336 |
| rs546996230 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882724 | TACTCTCTGCACCTC[-/CTT]CTTGCTCACCCCACC | 5336 |
| rs547008939 | snp | C/G | 0.000806614 | 0.0200663 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826873 | CTGGGTTTTTAAAAA[C/G]TTCTTCTTCTGTATC | 5336 |
| rs547011714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935457 | TTCTACCACATTCTC[C/T]AGGTAGCAAGCTTTT | 5336 |
| rs547012060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847685 | ATTTGAGAAAATTGC[A/G]TCTTACTGAACATGG | 5336 |
| rs547031524 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810148 | AGGCACTCACCACCA[C/T]GCCCAGCTAATTTTG | 5336 |
| rs547037780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954975 | TGTAAAAGTGTTCCT[A/G]TTTCTCCACAGCCTC | 5336 |
| rs547044485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878321 | CCAGGCACTGGATTC[A/G]GGTCCACCCTAACCC | 5336 |
| rs547049808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824709 | TAGCTGCCATGTGAC[C/T]TCTGGCCTTTTTGTC | 5336 |
| rs547073369 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826501 | AATCGCAATAATAGT[A/G]GGACCTATCTCACAG | 5336 |
| rs547084863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802424 | GCCTCAGGTGGGTAC[A/G]GTCTTATTCATGTCT | 5336 |
| rs547085754 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855987 | GAGCCCTGACCCCCT[C/G]TTCTTAATTTGGTAA | 5336 |
| rs547100313 | snp | G/T | 1.65666e-05 | 0.00287802 | missense | PLCG2 | GRCh38.p7 | 16:81931555 | CCTGGAGCCCAAGCA[G/T]CAGGGCGATCCTCCG | 5336 |
| rs547119719 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829374 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 5336 |
| rs547145624 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780576 | TCATTGTGAGCCTCA[C/G]TGATGTTTAAGTCAC | 5336 |
| rs547151963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910033 | GGTGGGGGAAGTAGG[C/T]AGAATGTTCTGGAAT | 5336 |
| rs547152035 | in-del | -/TTTTTTT | 0.458315 | 0.13822 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876017 | TTTTCTTTTTCTTTC[-/TTTTTTT]TTTTTTTTTTTTTTG | 5336 |
| rs547160957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832424 | AGACACGATCTCACT[C/T]TATCACCCAGGTGGG | 5336 |
| rs547179548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888557 | ATAAGATTTTATACA[A/G]TGCTTCATACAGTGT | 5336 |
| rs547185378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863031 | AAAATTTGTTTTATT[A/G]TGGTAACAACAATGA | 5336 |
| rs547216037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791726 | GGTACCATCACATGC[A/G]GCTAATTTTTGTATT | 5336 |
| rs547228346 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778490 | CCATCAAAGAGCATA[A/G]GAAGGGTTTGAATCA | 5336 |
| rs547256426 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911777 | CACTGGGCCTGGCTA[A/G]TTTTTGTATTTCCTT | 5336 |
| rs547264015 | in-del | -/T | 0.00240964 | 0.0346267 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891391 | GCTGTTCTTCCCCCC[-/T]GGTGGGCGCAGACCA | 5336 |
| rs547266219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866809 | CTCTCCCCACGACCC[C/T]TCTCGCTGCCGCTCT | 5336 |
| rs547267260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918525 | TTCCCCCTGGTGTGT[C/T]CTAGACATCTTTATT | 5336 |
| rs547276406 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789193 | CTTCTGAAGCTCATT[G/T]TGATGGGCATGAGAC | 5336 |
| rs547279179 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795838 | CCAAAGAGCTGGGAT[A/C/G]ACAGGCATGGGCCAC | 5336 |
| rs547279906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844205 | TTCACGTGTTAGCCA[A/G]GATGGTCTCTATCTC | 5336 |
| rs547283252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823499 | CTAGCTTGGATTTGT[A/G]TTGAAGGCTTTAAGA | 5336 |
| rs547296624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944643 | CTAAATTTTTTATTT[C/T]ATTTTATTTCTTGTA | 5336 |
| rs547300789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892043 | GGAGGAAGACCTCCA[C/T]TGAAAGTTAACCACA | 5336 |
| rs547301810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799717 | CCTGCCTCAACCTCC[C/G]GAGTAGCTGGGACTA | 5336 |
| rs547302013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870364 | CCATAAAGCAATTAA[C/T]TGGAGCTGAGTTCTG | 5336 |
| rs547321739 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948748 | AAAGTTGGTCAGTTT[C/G]CCTAATGCTGGCTCC | 5336 |
| rs547331665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918044 | CATTTTTAAATTGGG[C/T]CATTTATTTTCTTAC | 5336 |
| rs547341950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795515 | CCAGTGGGATTGGGG[A/G]TGGGACTCTGCTGTC | 5336 |
| rs547342997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842145 | CACCCCTGGGGAGCA[C/T]AAGCCAGGATTTGAA | 5336 |
| rs547374052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819002 | TTATTTCATCCTTCT[A/G]GGCCCACCATGAGGC | 5336 |
| rs547393559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835040 | GTTTTTCTCAGTGGG[A/G]GGAGGTGGAGGTACC | 5336 |
| rs547399544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781161 | ATCCTCTACCCTCTC[C/T]CAGCCTCCGATAAAT | 5336 |
| rs547400816 | in-del | -/ATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867425 | CAGTCAGGTGTGGTC[-/ATT]ATGGGCACACTGGGT | 5336 |
| rs547401475 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777398 | TACTAAAACAAAAGT[G/T]TGAAAAAGATTGGTT | 5336 |
| rs547403148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871824 | TGCAGCATTACTTAT[A/G]CTGGCAAAGTACCTG | 5336 |
| rs547404053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928089 | TGGTTCAAGGGTGCA[A/G]TGGGAGGCAGAGCTG | 5336 |
| rs547412601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849620 | ACATACACACACACA[A/G]ATTTTCCAGGTCTGG | 5336 |
| rs547415912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910799 | GCTGGCCTGGTGGTT[C/T]AGCCGGGCCAGTCCC | 5336 |
| rs547449691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853064 | GGCTGGGCCCGCTGG[C/G]TCACGCCTGTAATCC | 5336 |
| rs547450845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830191 | CAGGCATGTTGGCAC[A/G]CATCTGTGGTCCCAG | 5336 |
| rs547453385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805073 | GAACAACATCAGACA[A/C]TTTTCCCCAATCACC | 5336 |
| rs547456113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834733 | ACCCACTGGACCAAG[G/T]CATGGCTGCCCTTTA | 5336 |
| rs547456166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839112 | TTTATTATTTTGCAG[G/T]TCCTATTGTATATGG | 5336 |
| rs547457084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822621 | AATTAACTGGGCATG[A/G]TGGCGTGTACCTGTA | 5336 |
| rs547478513 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896137 | AGTTGCTCCCGGGCT[C/T]TAGAGCCCCGAGGAG | 5336 |
| rs547482290 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830895 | ATGTCCAGGCAGGAG[A/C]GGGGAGATGGACAGG | 5336 |
| rs547486872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888878 | ATGCCCATTTGCCTA[C/T]GGATCATCTGTGGCT | 5336 |
| rs547500252 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780571 | AATCGTCATTGTGAG[A/C]CTCACTGATGTTTAA | 5336 |
| rs547519674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812186 | TCCTGAGTAGCTGGG[A/G]CTACAGGCACCTGCC | 5336 |
| rs547523656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857023 | AATTCAGAGATCTCA[C/T]GCAACCAGTCTATTT | 5336 |
| rs547536815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852640 | GCAGAAGTTGCAGAA[C/T]GGAAGGATTTCTTAC | 5336 |
| rs547538259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907608 | AGATGCTGGGGTGAC[A/G]CCCTGCAGGGCTCCT | 5336 |
| rs547541084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903302 | TATGTTCCAGGAAGT[C/T]GTGGTTTGGTAGGGA | 5336 |
| rs547550801 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842382 | GACAGGGCCTGTCCT[C/G]CCTCCCAGACTCGGA | 5336 |
| rs547554995 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939797 | ATTTATTTACATGGT[C/T]GCTAAGGGGATTCAC | 5336 |
| rs547561522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834254 | TATTAAATGTTCAGT[A/C]AGGGGGACCTGGTTT | 5336 |
| rs547563493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780134 | CTAATCTTGAACTAG[A/G]GTGAGAAACTATGGG | 5336 |
| rs547577050 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885096 | TTGCTCTGTCACCAG[C/G]CTGGAGTACAATGGC | 5336 |
| rs547577861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798121 | CAGGTGTGAGTCACC[A/G]CGCCTGGCCTGAGTC | 5336 |
| rs547578504 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868553 | GAGTCTTGTTCATCC[A/T]TTCATGTGTGTCGCT | 5336 |
| rs547580826 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882622 | CCTCCCTCTGGCCTG[C/T]GTTCCCTCGCTCCTA | 5336 |
| rs547587640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865015 | GGTTTGTGTGCAGGA[A/G]GCTTACTAGGGAGTG | 5336 |
| rs547592899 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802516 | ATGTGTAACTGCTAC[C/T]TTGACCTACCACCTT | 5336 |
| rs547594293 | snp | A/G/T | 1.65649e-05 | 0.00287788 | missense | PLCG2 | GRCh38.p7 | 16:81956807 | TGCGCAATGCCAACC[A/G/T]GGATGCCCTGGTTAA | 5336 |
| rs547598304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901252 | CAGTTGCTAGAAAAG[A/G]CTGAGTGCAGCAATA | 5336 |
| rs547638042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846303 | CTCCAGACATCCCCC[C/T]GCCACTCCCTATACA | 5336 |
| rs547651610 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780186 | ACATGGCGCGAGGGA[A/G]ACAGGTGGCCTTGCC | 5336 |
| rs547659050 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942657 | AATCCTGTGAAAGGG[C/G]TTTTATCTTTGGTTT | 5336 |
| rs547665978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802198 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 5336 |
| rs547666808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920470 | AAAGCAAAGAAAACA[C/G]GATAGTGTGAAAAGG | 5336 |
| rs547673591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797610 | GCTCCTCAGATACCT[C/G]GTTAACAGATGAATC | 5336 |
| rs547682190 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896697 | CCACCAAACCTGTTT[C/G]TACAGGCGGAATCCA | 5336 |
| rs547686236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924619 | TGCTAAGTCCTTCCC[A/T]GTCCTCTTGCAAGAT | 5336 |
| rs547688606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897311 | ATGGGTTCTGAGTCC[G/T]TCTCGCTGAGTTTGA | 5336 |
| rs547706484 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881683 | GGAGCCTCCCTTTGT[C/T]GCCTAGGCTGGAGTG | 5336 |
| rs547711811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904378 | ATCCTGAGCTCCTTC[A/C]CCAGGTTACATGACC | 5336 |
| rs547717602 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849956 | ACCTTAATACCTTTC[A/C]AGTTTTTAGATAATT | 5336 |
| rs547731909 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882213 | CTCCCCATCCAACCC[A/G]GGGGTGGCTCGTGCT | 5336 |
| rs547739523 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953615 | ACTAAATTTTTAAGT[G/T]AAAACTCAGACTCAA | 5336 |
| rs547752820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872779 | ATGATCTTGGATGAA[C/T]CACTGACTGCTCCTA | 5336 |
| rs547758226 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821676 | GCCTCTGTAGAAAAA[A/G]ATGTATAAGCAGCGG | 5336 |
| rs547761833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925141 | CAGTTCTCTGAATTT[C/T]GAAGGCTCTTGTCTT | 5336 |
| rs547771055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908179 | TTGCTGGGAACCGTT[C/T]ACTGCATGTCTCAGG | 5336 |
| rs547772502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944691 | ATGTTGCCTAGGCTA[C/G]TCTTGAATTCCTGGC | 5336 |
| rs547788549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875917 | TTTGTGGAGGAGCTC[A/G]GAGATCTTGCAGTTT | 5336 |
| rs547791894 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808835 | ATAGCCTCTGTGGGC[C/T]TGGCCTCTGTTTCCC | 5336 |
| rs547827148 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824026 | TTCCTTTCCTTTCCT[G/T]TCCTTTCCTTTCCTT | 5336 |
| rs547833942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885337 | CCCCGACTAATTTTG[G/T]ATCTTTAGTAGAAAC | 5336 |
| rs547836109 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809880 | AAAGAGAATTTACTG[A/G]AACGTGTGGCTGAGA | 5336 |
| rs547837390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912277 | CATTGTGTTGGCCAG[C/G]CTGGTCTCAAACTCC | 5336 |
| rs547860565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860985 | CCGTCTCAAAAAAGC[A/G]AAACAAAACCAACCA | 5336 |
| rs547861996 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881162 | GAGCACTGGGAGGAT[-/G]GTCCAGAAAGTTCTG | 5336 |
| rs547875917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850568 | TCCCAGACAAGGCTT[C/T]ATTGGAGCTTATGCC | 5336 |
| rs547876054 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870011 | CAAGGTTCCTCAGTG[C/G]AAAAAGCTCATTTCA | 5336 |
| rs547877455 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875563 | AGCTGACTTCAGCCA[C/T]TATCACCTTGTCACT | 5336 |
| rs547879661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948798 | GTTTAACATCCATGA[C/T]CCAAGAGTGTGACAT | 5336 |
| rs547893882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804974 | AGTGTCTAGTCATTA[C/T]AATCTGTCTGTGAGT | 5336 |
| rs547897040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865335 | CCTGTGCTGGTTTTG[A/G]TCGGGCTGTGCAGCA | 5336 |
| rs547897107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936895 | TTTTATAGCCACATC[A/G]GATTCCACAGAATGG | 5336 |
| rs547905108 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789565 | AAGTGCTGGGATTAC[A/C]GACAGGAACTACCAT | 5336 |
| rs547921326 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897670 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 5336 |
| rs547938352 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913222 | TAATGACAAGGAGCC[A/G]AGGAGTGACTCAGAC | 5336 |
| rs547959925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936593 | GCTTACGCAGGCTTC[A/G]TGATTGTAAGTAAGT | 5336 |
| rs547963336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890089 | CCAGTGGGCGGTCCA[A/G]GTAGAGCCATGCGAA | 5336 |
| rs547971139 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961279 | ATTGAAAACGGAAAA[C/T]AGAATTGATGATGAA | 5336 |
| rs547971587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820022 | ACCCTCCAGGGAGCA[C/T]TGGACCCAAACTAGG | 5336 |
| rs547971881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824336 | ACAAGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 5336 |
| rs547978010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924654 | TAATCCAGGGATTAT[C/T]AAACTTTTTCTTAAA | 5336 |
| rs547992433 | in-del | -/CAAACAAA | 0.0263992 | 0.111815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957296 | AGAGGGAGACTCTGT[-/CAAACAAA]CAAACAAACAAACAA | 5336 |
| rs547994333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800990 | TGCAGGTGGCTTGTG[C/T]AAGCTGGAAAAGGCA | 5336 |
| rs547999334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940997 | GAGGTCACTGTTCCC[C/T]TGTTTTCTGAGGATC | 5336 |
| rs548004328 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894829 | AGTAAGCTGAGATCG[C/T]GCCGCTGCACGCCAG | 5336 |
| rs548006069 | in-del | -/T | 0.472616 | 0.113763 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799599 | CTGGCCTGTTATTAA[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs548024837 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825015 | CCACAAGCCAAGAAA[G/T]GCAGGTGGCCTCTAG | 5336 |
| rs548028697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876401 | AGTACCACTGAGTGC[A/G]TAAGACCAGCTTCGG | 5336 |
| rs548037721 | snp | A/C | 1.66018e-05 | 0.00288108 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81957974 | AAGAGAGAAGAGAGT[A/C]AGCAACAGCAAGTTT | 5336 |
| rs548041294 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784759 | CTGTTACCTTCTTTT[A/T]TGGGACTGGAAATGA | 5336 |
| rs548049635 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872217 | CCCGTAATCCCAGCT[A/T]CTTGGGAGGGTAAGG | 5336 |
| rs548063894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908281 | TTTCCCATACCCCTT[C/T]GGGTGGGGACCAGCT | 5336 |
| rs548067413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928927 | ATCTGTGTTTCCCAT[G/T]CGTTGCGAAGGAAAG | 5336 |
| rs548070433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819796 | TCACCATGTTGGCCA[G/T]GCTGGTCTCGAACTC | 5336 |
| rs548089839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853729 | TATTGGTTAAAACAG[G/T]TCACAGAGACAACCT | 5336 |
| rs548115309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831254 | TCGAGGCCAGGAATT[C/T]GGTCTGTTTTATTCA | 5336 |
| rs548119187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932686 | ACTCACTCAACTCTT[A/C]TGCAGGGAAGTGTCC | 5336 |
| rs548125277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805298 | AGGTCAGGAGATCGA[A/G]ACCATCCTGACTAAC | 5336 |
| rs548140787 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848772 | GAAGAAGGGTGTACA[A/G]TCCCTGCGTGTATGG | 5336 |
| rs548141086 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859666 | CAGCCTCCCAAGTAC[C/G]TAGGACTACAGGCAC | 5336 |
| rs548154541 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958556 | CTGCTGCAGTCCACA[A/T]GAAAATGGCTGAGTG | 5336 |
| rs548172281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901317 | TGATTATATCTGTGC[C/G]TAGGGATGCCATGGT | 5336 |
| rs548175376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935624 | CCTTCAGGGACTCAG[C/T]AGGCTCAGCATGTTG | 5336 |
| rs548177403 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849752 | CTCCAGCCTGGGCAA[C/T]AAGAGCAAAACTCTG | 5336 |
| rs548178480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831561 | TCATCCAACCCCATA[C/G]TCCAGTTGGGACCCC | 5336 |
| rs548190440 | snp | G/T | 6.72608e-05 | 0.00579878 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958040 | TGTGTGTGTGCGCAT[G/T]TGTGTTTGCATGTAG | 5336 |
| rs548202534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850083 | TAAACAAGGAGACTC[C/T]GTAGGATTGAAGATG | 5336 |
| rs548227560 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961662 | TGTTCCAGGTAAGAC[G/T]GATCATAAAAAAATG | 5336 |
| rs548239266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831350 | TAATGGCTGAATGAA[C/T]GGACGTGACCATCAT | 5336 |
| rs548239677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896704 | ACCTGTTTCTACAGG[C/T]GGAATCCAAGCAGCC | 5336 |
| rs548258728 | in-del | -/TATTTATTTATTTATT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81841239 | ATTTATTTATTTATT[-/TATTTATTTATTTATT]GAGATAGAGTCTCAC | 5336 |
| rs548282976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904592 | ACCCTGCCCAGCCTG[A/T]TCCCTCTGGACTGCG | 5336 |
| rs548288687 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914901 | TCTCAAAGAGTTGGG[A/G]TGTGAGGACTGATCC | 5336 |
| rs548288697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853400 | CATCATTTATGCCAG[C/T]GTGCCAGTGCTCCTA | 5336 |
| rs548290865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954077 | GCCCAGGCTGGAGTA[A/C]AGTGGCATGATCGTG | 5336 |
| rs548308855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781992 | TTCTCCTGCCTCAGC[C/T]TCACGAGTAGCTGGG | 5336 |
| rs548320011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885646 | TTTTAAAATATAGCC[A/G]TAACACTCCTCTTAC | 5336 |
| rs548342810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809304 | GGGGTGTTAGTGCCT[C/T]CAGGGGTGGCATGGC | 5336 |
| rs548348360 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830705 | ATTTTATATATGTAT[A/G]TATATGAATGAAATG | 5336 |
| rs548356059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839187 | TTAACATACATCAGT[G/T]CAGGTGAAAACGGTG | 5336 |
| rs548357289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835517 | CTGGGAGGTGGAGGT[C/T]GCTGTGAGCTGAGAT | 5336 |
| rs548358617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861077 | CCAAAACCAAACCCT[A/G]CCATTTATTGAACAA | 5336 |
| rs548392758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898030 | AAGTGCCAACCTCCA[C/T]CAGGCAGATGGAAGG | 5336 |
| rs548394222 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812520 | CATATCCTTTGTCCA[C/T]TTTTTGATGGGGTTG | 5336 |
| rs548409904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789895 | GCCCACTGTAGGCGC[A/C]GCCCTAGGCGCTAGA | 5336 |
| rs548421029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839588 | CTATTTTTAAACTTA[A/G]TTTTATATAGAAAAG | 5336 |
| rs548436769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888902 | TGTGGCTGCTTTTGC[A/C]ACACAACAGCGGAGT | 5336 |
| rs548445024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868947 | GGACATACCTGAAGG[A/G]TGGAGACCAGCCCTC | 5336 |
| rs548453764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828210 | AACAACTTGTGAAGT[A/C]TGTTCCAGACTGTTG | 5336 |
| rs548455920 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777533 | CTTCAAGTGGTTGAT[G/T]TCATAATGAGTCCTT | 5336 |
| rs548481728 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932287 | GGCAAGTAACCACAC[C/T]TCTCTGGGCCTCAGT | 5336 |
| rs548487854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798835 | GCCTCCCCGGCCTCA[A/G]GACTTCAGGGATCCC | 5336 |
| rs548501921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897752 | GTTTCACTATGTTGG[C/T]CAGGTTGGTCTTGAA | 5336 |
| rs548532839 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874984 | TTTTTTTTTATTTGA[C/G]ACAGAGTCTTTCTCT | 5336 |
| rs548535409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851243 | TTTCTGTGAACCATT[A/C]ATTTAGCTGCTCCAG | 5336 |
| rs548549651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917069 | TCCCCCTGCCCCGGA[C/G]CCTGGTAACCACCAT | 5336 |
| rs548559740 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864621 | GTGAGGCTTCAGGAG[-/T]TAATATGTGAAGGGT | 5336 |
| rs548560632 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902629 | CCACTTATGAGAGCT[C/G]TACCCTCATTCCCAT | 5336 |
| rs548574018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833380 | GCTCCGGTCGGTACA[C/T]GGGTCCTGAGCCAGT | 5336 |
| rs548595872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876781 | CACCCCTGTCCCTTG[C/G]TTAGGTAGAATCTGA | 5336 |
| rs548600455 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888613 | CTGTGTGGTAGATAC[-/T]TCTTATTCCCACTTC | 5336 |
| rs548608495 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959661 | AGAAAGAACATTCCT[C/G]TTAGTGGCAGATGTT | 5336 |
| rs548611568 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962168 | ACAAGCTCTCAAGAT[G/T]GCTGATCTAGGGCCA | 5336 |
| rs548628467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883766 | AGCCTGCCAGGTCCC[C/T]TGGGAGATAAACTAG | 5336 |
| rs548631814 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857547 | TCTGGTGAGGGCTCT[A/C]TTCCTGACTTGCAGA | 5336 |
| rs548635485 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908656 | ATGAGGCAGGGTGGC[A/G/T]AGTGGTTCTAGCTCA | 5336 |
| rs548645618 | snp | A/C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862849 | TGAGCTCCAGCCTGG[A/C/G]CAACAGAGTGAGATC | 5336 |
| rs548647478 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777861 | TCTCTAGTAAAAATA[C/T]AAAAAATTAGCCAAG | 5336 |
| rs548652364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805333 | TGAAACTCTGTCTCT[A/G]CTAAAAATATAAAAA | 5336 |
| rs548660025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855639 | AGTCGACTTGGGGAG[A/G]CAGATGTGTGTACTG | 5336 |
| rs548663018 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890294 | TTAGCTTTACAAAGG[C/T]AGTTTATTTTGGGGG | 5336 |
| rs548672855 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946767 | TTCCTCCTTTACGCC[A/C]GAATTCTTTCCTTAG | 5336 |
| rs548674079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808856 | TCTGTTTCCCCCTAT[C/G]CAAAATGGGGCTTAT | 5336 |
| rs548679654 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962715 | CAGAACTTTTTTTAA[A/T]AACTGCTATTCACCT | 5336 |
| rs548690512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835160 | CTTGTCTGCTTTGAG[A/C]CTTAGAATTTTATGT | 5336 |
| rs548698002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836681 | AGGAGGCTGAGGTGC[A/G]GTGAGCTGAGATTGT | 5336 |
| rs548706827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905862 | ATGGGATTTAGTCGT[A/G]TTGCCCAGGGTGATT | 5336 |
| rs548716180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887269 | GGACTACAGGCACCC[A/G]CCACCACGCCCAGCT | 5336 |
| rs548716914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861562 | TGCCCTGCCTGCTCC[A/G]CCACGCTGGGCCACC | 5336 |
| rs548717017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857243 | GGGACCTAAGTATTG[A/G]GGTTTTGAAAAGCCT | 5336 |
| rs548723810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880354 | GCCAATGTGCCTACA[A/G]TGTGCTGTGTCTACG | 5336 |
| rs548723877 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816574 | GCCTTGACCTCCTGG[G/T]CTCAAATGATCCTCC | 5336 |
| rs548756463 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893965 | CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 5336 |
| rs548760185 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81783503 | CAGTTAATATCTGGC[C/T]AGATGCTGCCACAGG | 5336 |
| rs548764720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845238 | GAGCCATTGTTCCCT[A/G]TCCCGTGTTATTTCT | 5336 |
| rs548771470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910434 | AGGTTGTGTGGCCAC[A/G]TGTAATGTCCCCGCC | 5336 |
| rs548779666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935028 | GGGTGGGGACACAGC[A/C]AAACCATATCACCCA | 5336 |
| rs548782619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899632 | TGCCATGTTTTTCCT[A/G]TTTTTGAGCTTTTTC | 5336 |
| rs548790974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945985 | TATGGACCAGTCAGT[C/G]ATGGCTGCCGGCCTC | 5336 |
| rs548797496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915437 | TCTTGGGCAGTGAAG[A/C]TGAGACCTCAGGCTG | 5336 |
| rs548802546 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848697 | CTTTCCTCTTTCCAA[C/G]AACTACTTATTGGGC | 5336 |
| rs548806205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810494 | GTCATTCTTGGTGAT[A/G]CAGACTGGTGAAAAA | 5336 |
| rs548809159 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873543 | TCAAGATAAGTAGTT[G/T]CAAATAACAGTTTTT | 5336 |
| rs548812101 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933668 | CTGTCAGGGTGTGGA[A/T]TGACTTAGGTAATAT | 5336 |
| rs548824078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798626 | ATACAAGTTGTGCTG[G/T]AGGCCAGGGGTAGGC | 5336 |
| rs548837372 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951835 | CCATAAATGTAAACA[A/G]CCAAATGAAATAATC | 5336 |
| rs548845490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829558 | ATACCTTTGCCAAAA[G/T]TGAGAAATTAACATT | 5336 |
| rs548851651 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779190 | GCGCTCCGAGAGGCG[C/G]ACCCGGCTGGGCGCG | 5336 |
| rs548852240 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802376 | CTCGGCCTCCCAAAG[A/T]GCTGGGATTACAGGC | 5336 |
| rs548865192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851036 | GCTTGTAGTAGAAGT[A/C]CTCAGTGGGGTGTGA | 5336 |
| rs548894080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796426 | CAGTATCCTTTGGCA[C/T]GGCCAGCCTTTCCTG | 5336 |
| rs548895300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899384 | ATACATACACGTTCA[C/G]ATGATATAGAAGGAT | 5336 |
| rs548896640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925818 | CTTGAACCTGGGAGG[C/T]GAAGGTTGCAGTGAG | 5336 |
| rs548900367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843456 | CATCATATTACACAG[A/G]GACAAGCGCTGATGC | 5336 |
| rs548902136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895754 | CCGGGGGCTGACCTC[A/G]GGGCTGTCAGTGAAC | 5336 |
| rs548902786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929256 | CCATGTGAAGGGACT[C/G]TGTAGCGGGCCTCCT | 5336 |
| rs548906672 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952141 | TTATATAAGAAAAAA[A/T]CATAAAATCTTATTA | 5336 |
| rs548908826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925542 | TCTGCTTATTCAGAC[A/C]AAAAAATTGTTAAGT | 5336 |
| rs548909875 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828528 | CAGGCGTGAGCCACC[A/G]CACCCGGCCGAGAAG | 5336 |
| rs548916197 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833095 | TTACAGCCAAGGTGA[-/G]GGTGCTTTCCTGCTG | 5336 |
| rs548919932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859844 | CCCGGCCACCAGGTG[A/G]TTCTAAGGGCTGGTA | 5336 |
| rs548923143 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802208 | AGCTCCGCCTCCCGG[G/T]TTCACACCATTCTCT | 5336 |
| rs548943015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923641 | AGGTGGGCTTGACTT[C/G]TCCCTTCTTGGTGAT | 5336 |
| rs548944312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911227 | GGCCGTATTACTTAT[A/G]GCAACTTTTTTTTTC | 5336 |
| rs548962325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930782 | ATTTAAATTATTTAT[G/T]CTTTATATGTAAAAG | 5336 |
| rs548969271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829170 | CTGGAGTGCAGTGGC[A/C]CGATCTCGGCTCACT | 5336 |
| rs548976675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803274 | CAGGTGCCCACCACC[A/G]CGCCTGTCTAATTTT | 5336 |
| rs548977302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783743 | TGGACCATGGGGGCA[C/T]CTTGTTCATCCCTTT | 5336 |
| rs548978200 | snp | C/G | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778680 | GAAACTGAGGCTGTC[C/G]GTTTTTAAGTGGTCT | 5336 |
| rs548980737 | in-del | -/GAG | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915803 | CCCCCTGCCTGCCCT[-/GAG]GAGCTCTTATAAAAA | 5336 |
| rs549005725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915458 | CCTCAGGCTGTGGCC[A/G]TGGCATCCACGCTCC | 5336 |
| rs549009467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864142 | CCCTGGAGGATTTGT[A/G]AAAGTGGAGGCTGCT | 5336 |
| rs549011963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910967 | TTGTCTTCATAGCCC[C/T]GAGACTTTGGGCTTT | 5336 |
| rs549011990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810803 | TTCTGATAGAAGGAG[A/G]CAGGGTCTTTAATTT | 5336 |
| rs549020371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880207 | GGTCGTGCCACTGCA[C/G]TCCAGCCTGGGTAAC | 5336 |
| rs549026033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915141 | TTTTGTGATGAGTGC[C/T]ACAAAGGGATTGGTC | 5336 |
| rs549037623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806894 | GGGGCAGAGTTATGG[A/G]GAGGAAGCAGGGGTC | 5336 |
| rs549043887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859391 | CCTCAGAGATGATCT[C/T]TGCCATGGGGCATTT | 5336 |
| rs549056147 | in-del | -/C | 0.00119784 | 0.0244435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883558 | TCTGGATGAGAAGAG[-/C]CTCATGTCGGGCCTC | 5336 |
| rs549057356 | snp | A/G | 0.000266476 | 0.0115398 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940087 | TTAATTAAGATGTTC[A/G]ATTTGGGCTGGCGTT | 5336 |
| rs549071357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811131 | GTCATATGGCACCAC[G/T]TATGACAGCAGTGTT | 5336 |
| rs549098168 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837688 | TACCAACATGTGTTT[G/T]TTTTTTTTTTTTTTC | 5336 |
| rs549106713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841127 | TCAGCGCAGTGGCAA[C/T]AACTCTGTTGTTTAT | 5336 |
| rs549124155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856888 | GTCATTCCCAGAGAA[A/G]GAGATGTGAGGATGG | 5336 |
| rs549130490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927849 | AGTGGGAGGTACAGT[C/G]TAAGCAAAGGTGTGG | 5336 |
| rs549132110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931929 | TTGATGATGTCTTTG[C/T]GGCCCTACATATCTT | 5336 |
| rs549142361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804562 | TCTGCTTTTTTTGTG[A/G]CACAAAAGGACCATT | 5336 |
| rs549143152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867142 | TGGGGACACAGGATG[G/T]CCAGAGTCACACTGG | 5336 |
| rs549149796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800532 | CATCTATGTCCCTGC[A/G]AAGGACACGATCTCG | 5336 |
| rs549168117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871175 | CCTTCCTGGTGGAAA[A/T]GCGAATGGCCATAAG | 5336 |
| rs549168483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871463 | TGTGCCTTAGCCTCC[A/C]CAGTAGCTGGGATTG | 5336 |
| rs549187197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947853 | GGGAGTTGAAAAGAG[C/T]CCCCCAGATAGCCTG | 5336 |
| rs549192635 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833373 | GACTGTGGCTCCGGT[A/C]GGTACACGGGTCCTG | 5336 |
| rs549194501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895485 | GAATTGCTTCAACCC[A/G]GGAGGCGGAGATTGC | 5336 |
| rs549203684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807908 | AACTCACTGAATATT[C/G]CAAGGACAGCACCAA | 5336 |
| rs549212092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856515 | GTATTAGCAAGCTCT[A/G]CTTGCTGTCCCTCTG | 5336 |
| rs549213586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822420 | GATGGGAGAGTATTC[C/T]GGGTTACCCAGGTGG | 5336 |
| rs549226292 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794800 | GGCATTGTAGAAAGG[A/G]TGGGATAAATACTAC | 5336 |
| rs549232546 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783934 | AGTTCAGATGCCTGC[-/T]TTTTTTCCCCTGAAA | 5336 |
| rs549242688 | snp | A/G | 0.000596086 | 0.0172536 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931573 | GGGCGATCCTCCGGT[A/G]GAGTTTGCCACAGAC | 5336 |
| rs549248921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860151 | TTATTTACTATTATT[A/G]TTATTATTATTATTA | 5336 |
| rs549255818 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877971 | TCCCTCTTTTTTTTT[A/T]AATTTTTTTTTTTTT | 5336 |
| rs549263468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780973 | TGGAGGTTGCAGTGA[A/G]CCCAGATCATGCCAC | 5336 |
| rs549288069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808367 | AATGTCCAGGGCACC[C/T]TTTTAGAGAGAGAGG | 5336 |
| rs549305871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788946 | AATACAGATGGGCCA[C/T]GTTGAGACTGGACTG | 5336 |
| rs549329828 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843392 | AGCTGAATCCAGTAC[A/G]TTCCTGAAAACACAC | 5336 |
| rs549355899 | snp | A/G/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877328 | GGGCATAGTGGCGGG[A/G/T]GCCTGTAGTCCCAGC | 5336 |
| rs549365076 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795581 | GGTGTTGGAGGCTAC[C/T]GCAGGATCCTTTGTG | 5336 |
| rs549368078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881240 | ATGAGATGTGACAGG[C/T]TAATAGTTTTTTTTT | 5336 |
| rs549375111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956398 | CATGTAGACCAAAGG[A/G]AAACCGGGTTAGATT | 5336 |
| rs549376414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939667 | ATGGGAGGTGGTCTC[C/T]TTCCTCTGCTCACCA | 5336 |
| rs549379885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884154 | CCAGGAGTTCGAGAC[C/G]TACCTGGCCAACATG | 5336 |
| rs549385543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888222 | TCAGAGTACTTTCTT[C/T]TTTTTTGAGACAGAG | 5336 |
| rs549409354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919965 | TGGGGAAGGGGTTGA[A/C]GTTTTCAGAGGGTGG | 5336 |
| rs549426049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880846 | TTAACAACAAAAATC[C/T]TTCCGTTTTTGCATT | 5336 |
| rs549429850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891833 | CTAGTAAAAACAAAA[C/G]TAACTTAGTTTATGT | 5336 |
| rs549430252 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829361 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 5336 |
| rs549445966 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959978 | AAAGAACCTGACATA[C/T]GGCGGCATAGGAAGC | 5336 |
| rs549453195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784447 | AGAGCAGCTTGGCAG[A/G]AGGCTGAGCCCGGCT | 5336 |
| rs549492465 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871785 | AAACATCGGGGCCTG[A/T]GAATATATTATCGGA | 5336 |
| rs549493641 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847360 | GAGCCTAATTACAAA[G/T]GCATGATTGATTAAA | 5336 |
| rs549500014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852590 | CTATCCTTGCCTGGT[A/T]GGTTTTGACCAGGAG | 5336 |
| rs549520462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902955 | AACAGCACGTGAAAG[G/T]CCCGCCCCCATGATT | 5336 |
| rs549530623 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848567 | GGTCTCTCTGTCCCT[C/G]TCTGTCTCCCTTGGT | 5336 |
| rs549534889 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878022 | AGTCTCGCTCTGTCA[C/T]CCAGGCTGGAGTGTA | 5336 |
| rs549556868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891965 | TAGGGAGTGTGTACC[C/G]TGTGCCTGCTGGGAG | 5336 |
| rs549558557 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907476 | CCAAAAAGAAGCTCA[A/C]ATACCAAAAGAAGCT | 5336 |
| rs549602721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834577 | CACGTGGTTGATAGA[C/T]CCTGGATCTGCAGAG | 5336 |
| rs549618922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807322 | GATTGGGGCAGTGTG[C/T]ATCTCTGCGAGGAGG | 5336 |
| rs549627949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936483 | GGTGTCCAAGAATGA[C/G]TGATTTGTCCGAGGG | 5336 |
| rs549629884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784858 | GCCTGGGGAGCGCCT[C/T]CACTCTAAGTCCTAT | 5336 |
| rs549630389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845680 | GTTGAGCGCAGTGGG[C/T]CTGACCGCTCTCTGT | 5336 |
| rs549635509 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960747 | TATGCTTTGTGACCT[A/T]GTTAAAATCTAAACT | 5336 |
| rs549640939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826820 | CGTGATTTTCTAGTA[C/T]GACTCTCAAGGCTGC | 5336 |
| rs549653453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935516 | GGGTGTTTTGAGCTG[C/G]TTCCATATCTTTCAT | 5336 |
| rs549659422 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833448 | GGAGGCACCTGGAAG[C/T]CCCTGGCCTCTCCTG | 5336 |
| rs549679223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837997 | TATATCTGCCATCAT[A/G]GTCAAGAGACTAAAG | 5336 |
| rs549703599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857067 | TCTCTAACAGTCTGA[A/G]AATAAATCTATATTA | 5336 |
| rs549704840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792824 | TGAGGATTATGGGAA[C/T]GACAATTTAAGATGA | 5336 |
| rs549718043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931411 | GGTGGTTGGTCCATG[A/C]GAGAAACAGCTCAGG | 5336 |
| rs549725520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833968 | CTTTAGCCAGAAGCT[A/G]GCAGGTTCACCCCAA | 5336 |
| rs549727841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779760 | TCCTCTTTTCGAGCG[C/G]CTCTGCGTGGGGTGG | 5336 |
| rs549747527 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884484 | GAAATCATCTTACCA[G/T]CTGCACAGCCACCGA | 5336 |
| rs549764301 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960246 | AGGAAAGGCACACAT[A/G]GTATGATGGCTCTTC | 5336 |
| rs549766071 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801158 | TGGGAATTCAGTAGC[A/G]TAGCGATTGAGAATA | 5336 |
| rs549768509 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911354 | TCCTGCTGTGATCTC[C/T]GTCTTCGATTTTCTG | 5336 |
| rs549774307 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838437 | TGCAGACATAAAAAA[G/T]AATGAGTTCATGTCC | 5336 |
| rs549785067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822756 | ACAAGAGCGAGACTC[C/T]ATCTCAAAAAAAAAA | 5336 |
| rs549798459 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81882683 | TTTTTCCTCGAGGCC[A/G]CTGCTTCTCTGGTTT | 5336 |
| rs549808670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911664 | CTCCCAGGCTGGAGT[A/G]CAATGGCACGATCTC | 5336 |
| rs549811753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833803 | TCCTCCTGCCTTGGC[C/T]TCCCAAAGTGGTGGG | 5336 |
| rs549823431 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911340 | AAACCTTGTGAAACT[C/G]CTGCTGTGATCTCCG | 5336 |
| rs549831552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789092 | TGTAACAAACCTGCA[C/T]GCTCTTCACATGTAT | 5336 |
| rs549831745 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896341 | AAGAGCCTGGGCAAC[A/G]TGGTGAAACCCCTTC | 5336 |
| rs549832924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856044 | AAGCCAGGATGTGAA[C/G]TTTGATATATATCCC | 5336 |
| rs549844000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874932 | GGTGGACTATTTGCT[A/G]GGCACTATCCTATGT | 5336 |
| rs549848370 | in-del | -/CCTTTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823946 | CCTTCCTCCCTTCCT[-/CCTTTC]CCTTTCCCTTTCCTT | 5336 |
| rs549850735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811067 | TACCAGAGGGACATG[A/T]GTGTGCACTTCCTGG | 5336 |
| rs549851135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803828 | CTGGGATTACAGGCG[C/T]GTACCACCACACCTG | 5336 |
| rs549860145 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884182 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 5336 |
| rs549872224 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81872343 | AAAACAAACACAAAA[A/G]CAGAGAATGCAATAA | 5336 |
| rs549873647 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941112 | CAATGAAGAGCTGAA[C/T]TGGATCTTTTTTGTT | 5336 |
| rs549882043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784234 | CCCCATTCCCCTCAT[G/T]TGCATCCTAGTCCCC | 5336 |
| rs549896487 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850370 | ACAAACAAACAAAAA[-/AG]TTTCAGTGCACGAAA | 5336 |
| rs549919646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834388 | TAGCCCAGGAGCCGG[C/T]GCGGGTGGTGTTGGA | 5336 |
| rs549926302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846069 | TGCCCCACTCAGCTC[A/C]CATTACCAGGCTTGT | 5336 |
| rs549947183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783861 | TACTCTGTTCTGCCT[C/G]CTAGCCTTTGCTTAA | 5336 |
| rs549950014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868414 | GGGTCCCCACTTACT[C/T]TGCATCCCTCTTGTC | 5336 |
| rs549965802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868265 | CCCAGGGCAGCCTGG[C/T]ACACAGTAGGTGCTC | 5336 |
| rs549969553 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81787297 | CATGATCATGGCTCA[C/G]TGCAGCCTCAGCCCC | 5336 |
| rs549980829 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838076 | TCTGTCTTTGAAAGA[C/T]ACTAATTTTCTTTTT | 5336 |
| rs549983020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864613 | GGGCAGATGTGAGGC[C/T]TCAGGAGTTAATATG | 5336 |
| rs549992846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853473 | TCCACAGATGGTGGG[A/G]GCAGTGGGGGGATTG | 5336 |
| rs550012282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871795 | GCCTGAGAATATATT[A/G]TCGGATTGTTTATTG | 5336 |
| rs550028025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915587 | TATGTTTTCCAAACC[A/G]TTCACTTACTGAGTC | 5336 |
| rs550035411 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908033 | CCTTAGATGGAGGCC[A/G]GTGCTCTGGCTTGGT | 5336 |
| rs550038578 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850681 | GCTAAAGTAGGCAGG[C/G]AGTGATATTTAAGCA | 5336 |
| rs550050360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777343 | ATAAATTATACATAT[A/G]TATGACTGAACTAAT | 5336 |
| rs550058930 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81859884 | TGGGTGATGTGATAA[C/T]GTATATTCAGTTTAC | 5336 |
| rs550061997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880245 | CCCCATCTCTAAAGA[A/G]ACCTGGCAGTGAGGA | 5336 |
| rs550063097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800912 | AGGGTCAGAGTCAGA[A/G]TGAGACTGGAAGATG | 5336 |
| rs550087451 | snp | A/C | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959123 | AGTGCTGGGTTGGGA[A/C]GGGAGGTGGTTGGTA | 5336 |
| rs550089491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805282 | AGGTGGATGGATCAC[A/C]AGGTCAGGAGATCGA | 5336 |
| rs550093636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924172 | GTTACCACTTCGCTT[G/T]TTAACCTTAGAAGAA | 5336 |
| rs550097777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871488 | GGATTGCAGACGTGC[A/G]CCACCACGCCCAGCT | 5336 |
| rs550099203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860565 | TTGTTCATCTGCAAC[C/T]GAGGCAACCAAGTGT | 5336 |
| rs550101495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852985 | TCTGACTTCTTACAC[A/G]GAGGCTGGCTTCCCC | 5336 |
| rs550122328 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800557 | ATCTCGTTCCGTTTT[A/G/T]TGGCTGCATAGTATT | 5336 |
| rs550131756 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937179 | GATCGTGGGCGGGGA[-/T]TGCAAATAGGTGGAG | 5336 |
| rs550164316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811958 | ACGCTGTCTTCCACA[A/G]TGGTTGAACTGATTT | 5336 |
| rs550165234 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811776 | GTCTATCATCGATGG[A/G]CATTTGGATTGGTTC | 5336 |
| rs550170960 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936567 | GGGATGAGAGGACCG[A/T]AGGCTGCTTGGCTTA | 5336 |
| rs550189118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864994 | GGAAACATGATCTGA[C/G]ACGCAGGTTTGTGTG | 5336 |
| rs550202114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928187 | GACATGGGGAGCCAC[A/G]GAAGGTTCTTGAGCC | 5336 |
| rs550212818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932029 | CCTCCTGACAGAAAA[C/T]GTTCACTGAGCTCAC | 5336 |
| rs550223317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913199 | ACGCCAGATTCTCCC[A/G]CTTCCACTAATGACA | 5336 |
| rs550226554 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815768 | TGCGCTATAATTGAG[C/T]AGTCTTAAATGACCA | 5336 |
| rs550293565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840373 | GGGCCAGATTGGCCT[G/T]GGGGGATAGTGTGAG | 5336 |
| rs550298174 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944618 | TACAGGTGTGCATCA[C/T]TGTGCCCAGCTAAAT | 5336 |
| rs550303834 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828948 | CAGGAGATCACAGAA[G/T]GAATTTCCTGTGTGG | 5336 |
| rs550322421 | snp | C/T | 8.45687e-05 | 0.00650209 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937941 | GCCAGGGGAGCCAGC[C/T]GCCCTCCCTGGGGGC | 5336 |
| rs550323438 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81940209 | GAGAGCAGGTGTACA[A/G]CCTGTCGTGTAGCAC | 5336 |
| rs550344305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940099 | TTCGATTTGGGCTGG[C/T]GTTGTACTTTGGTTT | 5336 |
| rs550347441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900921 | AAATCTGCTCTCCTT[A/C]CTAACACTGTGACCT | 5336 |
| rs550348129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802816 | CCTCAGGTGATCCAC[C/T]CACCTCAGCCTCCCA | 5336 |
| rs550351176 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915105 | GAGGAGGTTTGAGCA[C/T]ATAAGGAAATCAGTG | 5336 |
| rs550369570 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842228 | TTCCCAGGTGAGCTC[C/T]AGTCTGCAGAACTCA | 5336 |
| rs550380421 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928504 | TTTGGAAACGGGTTT[G/T]CTTTTTATTATTCCC | 5336 |
| rs550386012 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778569 | ATATTAGCTTCTTCC[C/T]ATGAGATCAGGAAAA | 5336 |
| rs550390828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854981 | TTGGGAGCCTGAGGC[A/G]GGCAGATCACTTGAG | 5336 |
| rs550393419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953400 | TGTGAGAACATTGTA[C/T]TATTACTGTACCTTT | 5336 |
| rs550396462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805015 | TTACTCCTAAGTACA[A/G]TGAGCTTCAGTGATT | 5336 |
| rs550419867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827161 | GGTAAGGTGCATGGT[A/T]AATCTCATACATTAT | 5336 |
| rs550441843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929582 | TGTATTTTTAGTAGA[C/G]CTAGGGTTTCGCCAT | 5336 |
| rs550443617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932314 | CAGTTTCCTTGTCTG[C/T]AAAATGAGGAGCCAA | 5336 |
| rs550450496 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882160 | GTGCTCAGGGAAACA[C/T]ACCCATTACCCTGGG | 5336 |
| rs550478842 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851119 | CCCCACAAGGTTTAG[A/C]GATACCACCCCCCTA | 5336 |
| rs550483481 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960244 | TCAGGAAAGGCACAC[A/G]TGGTATGATGGCTCT | 5336 |
| rs550496291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902300 | TTCCTGCAGCTATCA[C/G]AAAATACCCTAAGCT | 5336 |
| rs550499426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834661 | ATGTTCCTGAGAGGA[A/G]GATTCTGGTAGGACC | 5336 |
| rs550503525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938195 | GGTCAGCCTCTGGCC[A/G]GAAAGAGAAAGAAAA | 5336 |
| rs550505704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786915 | TAAACCATCCTACTG[A/C]GGCAAGCTCATTACC | 5336 |
| rs550510703 | snp | C/G | 0.00413411 | 0.045302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905547 | CCACTGCGGCCACGC[C/G]CCTTGCAGCTGCTTC | 5336 |
| rs550516313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817797 | CGGTTGTGATTCTTT[A/C]ACTTAACACATTTAT | 5336 |
| rs550524985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880130 | CCTGTAGTCCTAGTT[A/G]CGCAGGAAGCTAATA | 5336 |
| rs550535393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881732 | TCACTGCAACCTCCA[C/T]CTTCCAGGTTCAAGC | 5336 |
| rs550553312 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962599 | TAGAGAATTAAGTGA[A/G]TGAGTCACACAGATG | 5336 |
| rs550559884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813509 | GTTGTGATTTTTGCA[A/C]ATTGATTTTGTATCC | 5336 |
| rs550562083 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838997 | CTCTTAAAGGCTTCT[C/G]ATTTCCCTTTATGAC | 5336 |
| rs550571469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870748 | TTCAGCATGCCAATA[A/G]AATAGCATGCCATTT | 5336 |
| rs550578621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886400 | GCAGCACTTTGTGTG[C/T]AAATTAGTATGCCTT | 5336 |
| rs550579980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934369 | GAGGAAAAATGCAGG[G/T]CGAGCTGGGAAGATG | 5336 |
| rs550586909 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816325 | ACAGTGAGTCCAAAT[C/T]GTGCCACTACACTCC | 5336 |
| rs550593119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862086 | AAAGAAACTTTGACC[A/G]AGATGCCAATGAAAG | 5336 |
| rs550609525 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81916773 | CTCCTGAGTAGCTGG[G/T]ATTACAGGCATGCAC | 5336 |
| rs550610868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810149 | GGCACTCACCACCAC[C/G]CCCAGCTAATTTTGT | 5336 |
| rs550627011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836265 | ATGACTCTCCCAAGG[A/T]CACACAGTAAGGTAG | 5336 |
| rs550629419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866320 | ATGGGCTCCACTGGG[A/G]CACCAGCATGAGAGG | 5336 |
| rs550657161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926956 | TCACAGATAGTGACA[C/G]TGGTCACTTGGCCAC | 5336 |
| rs550666674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886168 | TGGTAGGGAGACTGG[A/G]GCGTGTAGATTTACC | 5336 |
| rs550674533 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81901045 | GATGTGAGGGAAGGC[A/G]TGCAGAATGCGTGCA | 5336 |
| rs550674575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917537 | GGGGTCCCCTTTTCT[C/T]CACATCCCCACCAGC | 5336 |
| rs550677687 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81946865 | GGGCTTTAGCAGAAG[A/C]CTTAAACCAGTGAGC | 5336 |
| rs550684519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803226 | TGGGTTCATGCCATT[C/T]TCCTGCCTCAGCCTC | 5336 |
| rs550685271 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816998 | TACCCATTTATTGCC[C/G]AGAAGGTGACGGGCA | 5336 |
| rs550695885 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795882 | CTCCCACCTTCTATT[C/G]AACAGAATTTGGCAT | 5336 |
| rs550716001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821803 | TTCCTACCCAAAAGA[A/G]AAGGTTTTACTGCAA | 5336 |
| rs550716488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939568 | CCAGGCTCTCCTCCC[C/T]TTTTGTCTTTTCCAA | 5336 |
| rs550719237 | in-del | -/CAGT | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885981 | TAATTTTATTGGGCA[-/CAGT]CAGTCACGTTAGGTC | 5336 |
| rs550722007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951513 | TTCATTTAAATAACG[C/T]AATTCCAATTTCACT | 5336 |
| rs550723670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942224 | TAACCCCTCCCAGTG[C/T]CTTGCAGAGATGTCA | 5336 |
| rs550724752 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828739 | CAGCCTCAGCCTTCC[A/G]AAGCTGCTGTGATGA | 5336 |
| rs550731344 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813815 | CAGCATGGTGGTCTC[A/T]TAGTAGCTAGTCTTC | 5336 |
| rs550739233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806732 | GGACATGGAAGGCCT[C/T]ACTGAGAAGCTGGCA | 5336 |
| rs550740934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883798 | ACAGCTTTCCTTAAA[C/T]AGGTGATGCCTGGGA | 5336 |
| rs550763467 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829327 | TTGGTCAGGCTGGCC[C/T]TGAACTCCTGACTTC | 5336 |
| rs550765886 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801590 | AGCAAACACGTCTTC[A/G]CTATTGTTTGAAATT | 5336 |
| rs550774055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877229 | GGAGGCCAAGGCGGG[C/T]GGATCGCGAGGTCAG | 5336 |
| rs550777865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943631 | CAGGCCTCACCCCAG[A/C]CTTCCCAAGTCAGAA | 5336 |
| rs550795117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955490 | ATTGAAACCCAAACT[A/C]CCTACCCTGAGTGGC | 5336 |
| rs550797254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828725 | GAAGCCAGCCGTCAC[A/G]GCCTCAGCCTTCCGA | 5336 |
| rs550797357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832909 | GCGTGTGAGGCCCAG[A/G]CAGCCAGTGGTCAGC | 5336 |
| rs550805290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955018 | TGTTTCCTGACTTTT[C/T]AATATGCTTTATTCT | 5336 |
| rs550821543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905113 | GCTGGTCTAGAACTC[C/T]TGAGCTCAAGTGATC | 5336 |
| rs550822638 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875299 | CATTTAATTCCCCCC[-/T]AGAGGCCTGTGCAAG | 5336 |
| rs550824530 | in-del | -/GGTCG | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833369 | CTGGACTGTGGCTCC[-/GGTCG]GGTCGGTACACGGGT | 5336 |
| rs550829303 | in-del | -/ACTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886699 | CTCATGACTGGGACC[-/ACTT]ACTTAATGACTAGAA | 5336 |
| rs550846972 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939156 | CGGAATCGTAGGTGA[C/G]GCCCTGACACTAGGT | 5336 |
| rs550853368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813992 | AGAGATGGAGACCAT[G/T]GTATTCAGGGGCATC | 5336 |
| rs550854944 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81906517 | ACAGACTCCACCTCC[C/T]GGTTGAAGTGATTCT | 5336 |
| rs550855367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818077 | CTCTGTCGGCTCGTG[A/T]CCCCTGATCTGTGAA | 5336 |
| rs550861052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810840 | CCTTATTGTTTAGTG[A/G]GAGAGGCAAGCACAA | 5336 |
| rs550868002 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959002 | CCCTTGGGGCAGATC[C/T]ACCTAGTTCATGACA | 5336 |
| rs550895320 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782481 | CTCAAGGTCTTGGAG[A/C]CCTCCCTGCCATAGT | 5336 |
| rs550903162 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875756 | AAATAGAAAGCACTT[A/G]CAAAAAATCAAAAAG | 5336 |
| rs550908726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943272 | TGGCTCACAGTTCTG[C/T]AGGCTGTACAGGCTT | 5336 |
| rs550915943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867188 | GCGGCTGGGCAGTGA[C/T]GCGCTACTTCCTTCC | 5336 |
| rs550925086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877548 | CAGGGCCACACCCCT[C/T]GGAAGGCTCCAGGGA | 5336 |
| rs550925820 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864772 | ACGGGGCTGCCATCC[A/T]TAATGGTTTGGTGAT | 5336 |
| rs550949112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914587 | TTTTTATTTTTTAGA[A/T]GTTAATAGATGTTTG | 5336 |
| rs550955628 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963051 | TTTCTTGCCAACAAT[C/T]CCTGGTCCACAGGAA | 5336 |
| rs550959258 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887320 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 5336 |
| rs550968582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844619 | GAGCCACTGTGCCTG[G/T]CCCACACCTTCACTG | 5336 |
| rs550969450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867570 | AACAGGTGAATGTGC[A/G]TATAAGGCACCACCT | 5336 |
| rs550976832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946989 | CCCGGGGAAAGGGAA[A/C]CAGTGCTGCTTCTCT | 5336 |
| rs550985103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918678 | TTTTGAAGTAAGATA[A/G]TGTGCTATCTGCAGC | 5336 |
| rs550988612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895284 | GAAGCATTGAGGTTG[C/G]GCGTGGTGGCTCACG | 5336 |
| rs550992405 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962675 | AAAAATAAAAGTTTC[A/G]TCTGAATGAATATAG | 5336 |
| rs551015090 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899287 | ATATATATATATATA[C/T]ATACACACACACACA | 5336 |
| rs551024662 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791810 | CCTCTCGTGATCTGC[C/G]CACCCTGGCCTCCCA | 5336 |
| rs551027211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909618 | GCTGGAGTCTCACTA[C/T]GTTGCCCAGGCTGGT | 5336 |
| rs551037237 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867022 | GTCTGTCTGTGAAAG[C/T]CGTGGGTGCTGTCCC | 5336 |
| rs551048207 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933879 | TTAGATTTGATGGTG[C/G]GTCTTCTGAAGGGAG | 5336 |
| rs551050517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922963 | AATGTCAGGGTCCTG[C/T]AGGAGTGTAGATAGG | 5336 |
| rs551063750 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890640 | AGAATGGTTGCCTTT[C/G]ACCTTGCATAGGGAA | 5336 |
| rs551077315 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844003 | TTTTTTTGAGAAGGC[A/G]TCTTGCTCTGTGGCC | 5336 |
| rs551089356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951073 | GCTCACTGCAGCCTT[C/G]ACCTCCTGGGCTCAA | 5336 |
| rs551095744 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825176 | TTGTGTTGTTGTAAG[A/C]CACTAGGTTTGTGGG | 5336 |
| rs551111481 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935183 | GCCAGCAGGGCTGTG[A/C]TCCCTCCGGAGGGGA | 5336 |
| rs551124234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935136 | CTGGAGGCCAGAGTC[G/T]GAAATCAGTATCATG | 5336 |
| rs551124901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891352 | CTGAGGTCTGGAGAC[C/T]GCCTGTTGATTTCCC | 5336 |
| rs551127753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898966 | GAGGCGGGTGGATCA[A/G]CTGAATTCAGGAGTT | 5336 |
| rs551137048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910019 | ATGGGGTGGGGTGGG[G/T]TGGGGGAAGTAGGTA | 5336 |
| rs551138927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862960 | AAATGCAGAAATCTT[C/G]CCTTCCCCACCCTGA | 5336 |
| rs551140612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905903 | GGGCTCAAACAGTCC[A/T]CCCACCTTGGCCTCT | 5336 |
| rs551145542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799810 | GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 5336 |
| rs551146208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859465 | TACAGCAGTAACCAC[A/G]CTCCTGATGGCACCA | 5336 |
| rs551151875 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852222 | TGGGAGCAGCCGTGG[A/C]GGGGAGGTTTTACCA | 5336 |
| rs551151960 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818642 | ACAGAGCCAACTAGC[C/T]GGGCATACCTTTTCT | 5336 |
| rs551177431 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910873 | GAGGTGGCCAGTTTC[C/G]AAATTCCTGGCACCA | 5336 |
| rs551191112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851827 | CTTGTTTTCACATGG[C/G]TTTTGCCCACTGAGC | 5336 |
| rs551191301 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962028 | CCCTTCCTACCTCAC[C/T]GCTCCATGTGCGTCC | 5336 |
| rs551217821 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923428 | ACCTGGGAACGCAGC[C/T]GCCTCCCTCCCCTCC | 5336 |
| rs551223012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791468 | GTAGCCTGGACTGAG[A/G]TCATTTGGTGTCACC | 5336 |
| rs551227320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792234 | CACCTGTAATCCCAG[C/G]ACTTTGGGAGGCCAA | 5336 |
| rs551235841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905841 | ATTTTTTGTATTTTT[A/G]CAGAGATGGGATTTA | 5336 |
| rs551258241 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890411 | TAAAGGCAAGATAGA[G/T]GTTGGTTAGATCAGA | 5336 |
| rs551264866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831555 | TGAACCTCATCCAAC[C/T]CCATACTCCAGTTGG | 5336 |
| rs551277164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855325 | CACATGCACTTTCCT[C/T]ACTTTACTCAGGGGC | 5336 |
| rs551288377 | in-del | -/T/TT | 0.0879776 | 0.190697 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783833 | AACTCTCAGCAGGGT[-/T/TT]TTTTTTTTAGCATAC | 5336 |
| rs551315033 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927003 | TCAGAATTGAGCCAG[A/C]AGCCGGGTGCAGATG | 5336 |
| rs551334338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863525 | TGGGTGTACAAATCT[G/T]TTTGAGTCTCTGCTT | 5336 |
| rs551334648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845066 | CTTGAGTAGCTGAGA[C/G]TACCAGTGTGCACCA | 5336 |
| rs551334662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840778 | TTCATGGCCTGGGGA[C/T]TGGGGACCCCTGTCT | 5336 |
| rs551337859 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804683 | GGTTTAACGCCTCAG[C/G]CCAGGGAGTGTATAT | 5336 |
| rs551341580 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939331 | GCAGGAGGGACAAGA[G/T]GAATGCTTGCTCTTC | 5336 |
| rs551355778 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959626 | GGGAGCTGCTATTTT[A/G]TTTGGCAGTCAGCAA | 5336 |
| rs551364508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832562 | GCCCAGCTAATTTGT[A/G]TGTGTGTGTGTATGT | 5336 |
| rs551368294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787438 | ATCTCACTATGTCCA[C/G]GCTTGTCTCCAATTC | 5336 |
| rs551373819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829120 | TTTATTTTATTTTAT[C/T]TTTTTTGAGACGGAG | 5336 |
| rs551405026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858541 | TTTTTCAAATAAGAG[C/G]ATTTCCCTGTGCTAG | 5336 |
| rs551411097 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846038 | GAACGATGAGTTAAT[A/G]CAGAGGATGCTGTTG | 5336 |
| rs551419582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883170 | GCCAGACTAAGTGGG[A/G]CGTTCTGGGTGGCAG | 5336 |
| rs551420176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796329 | GGTTTTGCAACCTCC[C/G]AAGGATGGACCCCTG | 5336 |
| rs551432574 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839255 | GCAGTAGGCAGATAC[A/G]ACAAACCTTATAAGG | 5336 |
| rs551435288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832944 | ACTTGAAGGCCTCCT[C/G]TGTGCCCAGCTTGCT | 5336 |
| rs551439029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810203 | ACCATCTTGGCCAGG[A/G]TGGTTTCTATCTCTT | 5336 |
| rs551447612 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943658 | AGAATCTGCATTTTA[A/T]CAAGATTCACAGGTG | 5336 |
| rs551464971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915097 | GAAGCACTGAGGAGG[C/T]TTGAGCACATAAGGA | 5336 |
| rs551475710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923240 | CCTAACTCCTAACCC[C/G]TAACCCTTAACCCCA | 5336 |
| rs551487760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867134 | GCTGGAGGTGGGGAC[A/T]CAGGATGGCCAGAGT | 5336 |
| rs551532903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931220 | TATTGAGATCCTTAA[A/C]CTAAGTACATCTGCA | 5336 |
| rs551539187 | snp | A/C | 3.31214e-05 | 0.00406935 | missense | PLCG2 | GRCh38.p7 | 16:81880913 | TTTCCATTTCAGATT[A/C]TCGATGAATTCAAAA | 5336 |
| rs551550646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938339 | AATTTTTGAAAAGTA[C/G]AGAAATGAATTGCAT | 5336 |
| rs551553353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845100 | CACTTGGCTAACTGC[A/G]TTTATTTTTTGTATT | 5336 |
| rs551558751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821897 | TTTCCAGAGCAGCAC[A/T]AAGAGAGAGCCAGAC | 5336 |
| rs551564357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899004 | AGCAGCCTGGCCAAC[A/G]TGGTGAAACCCTATC | 5336 |
| rs551564528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826087 | TGTCACCAAAACAAC[A/G]GAGATCTCTGCCTTT | 5336 |
| rs551587469 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894433 | GACTCTGTGTCTAAA[C/G]TGAAAAGAAAAGAAG | 5336 |
| rs551604846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811103 | CCCTGAGGTGTTCAG[C/T]GTGCTGGGGAAGGTC | 5336 |
| rs551616235 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877632 | AAGCATTCCTCGGAG[G/T]GTGGACACCGCCTGG | 5336 |
| rs551626209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902333 | GTGGGTTATAAACAA[C/T]AGGAACTGATTTCTC | 5336 |
| rs551626671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825574 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGCGCC | 5336 |
| rs551653161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877406 | CTTACAGTGAGCCGA[C/G]ATTGCGCCACTGCAC | 5336 |
| rs551663713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930174 | AGAGCTCAAAATTAA[A/T]AAAATAAAATAAAAT | 5336 |
| rs551665484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810860 | GGCAAGCACAACATT[C/G]ATCAAATAATTTTGT | 5336 |
| rs551676729 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960261 | GGTATGATGGCTCTT[C/T]CCAGAGTCTATGTGA | 5336 |
| rs551692676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833841 | GCATGAGCCACGGCG[C/T]CCGGCCTCCTGTGTG | 5336 |
| rs551718964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869362 | AGCCTCTCTCATGAA[A/G]CCGTGGCTTGCCTTT | 5336 |
| rs551734468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859783 | CCTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 5336 |
| rs551737126 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880176 | AGCTCAGGAGAGTGA[C/G]GCTGTGGTGAACTAT | 5336 |
| rs551741568 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907054 | AAAAAAAAAAAAAAA[-/AA]CAGTGCAGCACACCA | 5336 |
| rs551750677 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798979 | GGAAAAGCCCCTACA[-/C]CAGGTAGTAGCATGA | 5336 |
| rs551750913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910900 | ACCATGACCTGTGTC[C/T]TTTTCTCTTTTCTTT | 5336 |
| rs551765353 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832280 | CTCTCTCCTGGGCTC[C/T]GCTCCACATGGCAGC | 5336 |
| rs551771729 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962063 | CGAAGCTGCGCGCTC[A/C/T]GTCGAAGAGGACGAC | 5336 |
| rs551778837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895634 | ACTTGCATTATGTAA[A/G]CGCACAGGGAACCCT | 5336 |
| rs551788374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921467 | ATGTTAATAGAATTC[C/T]ATCCAAATGCAACAG | 5336 |
| rs551790141 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851783 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGGGC | 5336 |
| rs551795065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914680 | AGCCCAGTCCTTGCT[C/T]TCTCAGGCTAATGGT | 5336 |
| rs551802158 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821560 | GTGGGTCCTGGGGGC[C/T]CCTGGCTGCTCAGTG | 5336 |
| rs551824696 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891305 | CTGCAGCCCATTGCA[C/G]CCTGAGCCTTCGGTA | 5336 |
| rs551840306 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893120 | CGCCTCAGCCTGCCA[A/G]AGTGCTGGGATTACA | 5336 |
| rs551842486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820331 | ACCCTCCCCAGCATG[C/T]ACACTCCCTGCCCCA | 5336 |
| rs551849776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925475 | CGTGAAAAGGGCTTA[A/C]AACCCGCAGTCCTGT | 5336 |
| rs551864616 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956459 | TTATTTCAATGTTTT[G/T]CAATAAATCAACAGT | 5336 |
| rs551864669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846980 | ATTCTGATACTATCT[A/G]CTTGGAGCTAGAATC | 5336 |
| rs551872653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925074 | ACTACTCCAAATCAC[G/T]GTTTTCCATTCTGTG | 5336 |
| rs551872942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797760 | CGTGGTTCCACTCGT[A/G]GTCCTGGCACTTAGT | 5336 |
| rs551874122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801766 | GCTCACTGCAACCTC[C/T]GCCTCCAGGGTTCAA | 5336 |
| rs551897355 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848703 | TCTTTCCAAGAACTA[C/G]TTATTGGGCCCCGCT | 5336 |
| rs551900743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822306 | AAGCATGATTGATGG[C/T]CCCCAGAGATGTCCA | 5336 |
| rs551909121 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865391 | AGTGAGGGAGGGGCT[C/T]GCCTAGGGAGAAAGC | 5336 |
| rs551911962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860061 | CTGCAGCCGTAAAGT[A/C]CTGGGCTCAAACGAT | 5336 |
| rs551919741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916698 | TCTGGAGTGCAGGGG[C/T]GTGATCTTGGCTCAC | 5336 |
| rs551928289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884404 | AAAAAAAAGTCAAAG[A/T]AGTATTCAGCACCAA | 5336 |
| rs551935824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952048 | GGTGTGGGAGGAAGG[C/G]ACAAATGGGACATCC | 5336 |
| rs551983623 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960037 | TGTGTAAAATCCATG[A/C]GTGGCCAAAGAGAAG | 5336 |
| rs551984202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812579 | TTGTAGATTCTGGAT[A/G]TTAGCCATTTGTCAG | 5336 |
| rs552007027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906679 | TCTGCCCGCCTTGGC[C/T]TCCCGAAGTGCTAGG | 5336 |
| rs552013434 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784305 | TTCCCCAATGGCTGA[C/G/T]TAATGCTAACTGAGA | 5336 |
| rs552016464 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955569 | AACTGAAAAGTTTAG[C/G]GGTAGGTCTTGTTTC | 5336 |
| rs552022155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949218 | TAAACAGACGGTGGA[A/G]AGCTATTAATGAAAT | 5336 |
| rs552029347 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865758 | CACTGGGGCAGCAGC[C/G]TGAGAGGACGCTGGC | 5336 |
| rs552035241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937405 | GTATCTACTGCAGTA[C/G]GTATTTATAGCATAG | 5336 |
| rs552036893 | snp | A/G | 3.31214e-05 | 0.00406935 | missense | PLCG2 | GRCh38.p7 | 16:81940001 | TTATGAAGAAGATAT[A/G]TTCAGCGATCCCAAC | 5336 |
| rs552057511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814970 | AGCTGCTGGAGATGG[A/T]GGCGATAAGAAGTTA | 5336 |
| rs552067062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886026 | AGTGAGGTAGAGAGA[A/G]ATTCATGCACTTTTT | 5336 |
| rs552074427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837639 | TCTCAGTTCCCTTTC[C/T]GTCTTCCTGATTATG | 5336 |
| rs552076757 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783950 | TTTTTTCCCCTGAAA[G/T]CTTTTTCTGAGCCCT | 5336 |
| rs552078931 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81869868 | GCAGGTGAGGCAAGG[A/G]TGGAGACAATGGGCA | 5336 |
| rs552086506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792745 | ACTCACTATCACGAG[A/G]ACAGCATGGAGGTAA | 5336 |
| rs552103264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887791 | GAATTTACATGTCAT[A/G]TTTCATCCCCTTTTC | 5336 |
| rs552113048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945594 | GGTGGGGGAGATTCG[A/G]CTCCAACTTGCCCCC | 5336 |
| rs552117868 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961710 | TTTAAAAAGATCATA[G/T]TATCTATCAAATAAC | 5336 |
| rs552125360 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847543 | AAAAAGATACTTATC[A/T]CTGCAGATTCCAAGG | 5336 |
| rs552127039 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941407 | CAGGGTGGGGCCAAG[C/G]AATCTGCATCTTTAG | 5336 |
| rs552135876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837181 | ACGAGAATACATATA[C/T]ATGCAGTGCTGCTTC | 5336 |
| rs552147196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950256 | TAGGAATGGATGGAA[A/G]AGTTACTGGGAAAAT | 5336 |
| rs552149398 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954837 | TAGAATGATTTATAT[A/T]CCTTTGGGTACATAC | 5336 |
| rs552157130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790375 | TTGCAATGATGGTGT[C/T]GGTAAAGTGACAGGG | 5336 |
| rs552174232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949668 | GAGGGAAACCAGTGA[A/G]TAATTAATTTTGCAG | 5336 |
| rs552176939 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858996 | CCCTTGTTAGAAAGT[A/G/T]GGAAGACTCCTCCTT | 5336 |
| rs552177817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828301 | CCCAGGCTGGAATGC[A/G]GTGGTGTGATCTCGG | 5336 |
| rs552180760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842813 | TAAAGCGGGGAGTGA[A/G]AGGAAGCTATGAGAC | 5336 |
| rs552189514 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884299 | GAGGTTGCAGTGAGC[C/G/T]GAGATTGCGCCACTG | 5336 |
| rs552193116 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893453 | AAAAGAACACGTCCT[C/G/T]TCCACGCTTGCATTG | 5336 |
| rs552204353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879565 | ACCCTGATAGTCCCC[A/G]TGACGTCCTGGGCTG | 5336 |
| rs552223779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897612 | GTGCAATGGCAGGAT[C/T]TCGGCTCACTGCAAC | 5336 |
| rs552239163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827959 | GCCAGGCATGGTGGC[A/G]GATGCCTGTAATCCC | 5336 |
| rs552267530 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799114 | TCCCTCTGGCCTTGC[A/G]TATTTCTCCTAATTA | 5336 |
| rs552276291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876076 | TGTCACCGAGGCTGG[A/G]GTGCAGTGGTACAAT | 5336 |
| rs552285788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901946 | CTGTAGCTTTCCCCA[G/T]ATTTTGAAGGAGCTC | 5336 |
| rs552286962 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81954883 | CTGGGTCAAATGGTA[C/T]TGCTGGTTCTAGATC | 5336 |
| rs552292359 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861560 | AATGCCCTGCCTGCT[C/G]CGCCACGCTGGGCCA | 5336 |
| rs552301152 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935687 | AGAGAAGATGAGGCC[A/T]GTCCCCTTCCCTCTC | 5336 |
| rs552301401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857638 | GGAGCTCTAGTCTCT[C/G]TTTCTCTTCTCTAAA | 5336 |
| rs552303168 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786757 | TAAAGTTTCTAAGAC[G/T]GTTTTTAACAAATAG | 5336 |
| rs552306255 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785178 | CCAAGGTTTTGGGCC[C/T]AAGCACCTCTCTGAC | 5336 |
| rs552322272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929494 | TCTGCCTCCTGGATT[C/T]AAGTGATTCTCCTGC | 5336 |
| rs552332903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805865 | GAAGTGAATCAAACT[C/T]CTGGGCTCAAGTGAT | 5336 |
| rs552343202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890253 | CAGAATCCAGGCTCC[C/T]CTCATCCTCCTAACC | 5336 |
| rs552358807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835557 | GCTCTCTAGCCTGGG[C/T]GACAGAGCAAGACTC | 5336 |
| rs552370932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811469 | CAGGATGATGTTTCC[A/G]TTTTCTTTTTTCTTT | 5336 |
| rs552379196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896607 | CAAAAAAACAAAAAC[C/T]AAAAAAAAAGTGAGG | 5336 |
| rs552387459 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891008 | TCTCTACTAAAAATA[-/C]AAAAATTAGCCTGGT | 5336 |
| rs552404944 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915502 | ATGCAACTCGTATTC[C/T]AGACCTGTTCCCATC | 5336 |
| rs552406133 | snp | A/C | 0.121022 | 0.21416 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858091 | CCATCTCAGACAAAA[A/C]GCAGGTCCTAGGGCC | 5336 |
| rs552407627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912793 | AGACAAGGGGGAACT[G/T]CAGGTGGAGGCTCAC | 5336 |
| rs552409251 | snp | C/G/T | 0.000118993 | 0.00771256 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81785958 | CTTCCTGATTTCTCC[C/G/T]GATTCCTTCCTTCTC | 5336 |
| rs552438794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835950 | GTCTTGGGTTAGGAC[A/C]CACCCTAATCCAGCA | 5336 |
| rs552448947 | snp | A/G | 0.000336844 | 0.0129734 | missense | PLCG2 | GRCh38.p7 | 16:81889203 | ATCTGAACAAAGTCC[A/G]TGAGCGGATGACAAA | 5336 |
| rs552451915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946770 | CTCCTTTACGCCAGA[A/G]TTCTTTCCTTAGGAT | 5336 |
| rs552464280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817428 | TTGAGAAGGAGTTTC[A/G]CTTTTGTTGCGCACG | 5336 |
| rs552468151 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81851241 | AGTTTCTGTGAACCA[G/T]TCATTTAGCTGCTCC | 5336 |
| rs552470279 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944823 | TCCAAGGATTTTGGT[A/G]TCTGGGGAGGTCCTG | 5336 |
| rs552471588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785789 | GTCCTGCCTTAGCTC[C/T]CTGAGTGGCCAGCGA | 5336 |
| rs552473532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839678 | ATACTACAGTTAAGA[C/G]ATAACAAAGGGTGGG | 5336 |
| rs552477311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789912 | CCCTAGGCGCTAGAG[A/G]TACAGCAGTTATTAA | 5336 |
| rs552483090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950602 | CTCAAACTTCATAAA[C/T]TTGATTGCATTCGTT | 5336 |
| rs552506743 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839382 | CTCTATATAGTCTTT[A/G]TATAATGAGAGTTTT | 5336 |
| rs552535809 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930569 | CCCTGGGCAACATGG[C/T]GAAACCCCTCTCTAC | 5336 |
| rs552539905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898074 | AGACACTGTGCAGTG[A/G]CAGCTTACACTCTGC | 5336 |
| rs552557497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800033 | ATTTGTGGCCATGGA[C/G]AAGTTACTTAACTTT | 5336 |
| rs552562310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847630 | CCTCTGTATTTGTGG[A/G]TTCTGCGTCTGCGGA | 5336 |
| rs552574366 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778107 | CTATAACAGACCAGT[A/G]GCACATGCCTGTGAT | 5336 |
| rs552597943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851305 | AACCTGGACATGGTC[A/G]CTGGTGCAGTGCTAT | 5336 |
| rs552610533 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958632 | TGTTTTGTGACTAGA[A/G]TTACTGGGATGGAGG | 5336 |
| rs552622829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877187 | GTGTCGGGCACGGTG[C/G]CTCACGCCTGTAATC | 5336 |
| rs552630908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898453 | TGGATCAGGATCGGG[G/T]AGTGAGCTGGGTCCA | 5336 |
| rs552644856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865551 | CTGGGTTTTCTCCAC[C/T]TGTTCTTGAGCAGCT | 5336 |
| rs552646904 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860857 | GCTCCTGTAGTCCCA[C/G]CTACTCAGCCTCAGG | 5336 |
| rs552676467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904644 | CTAGAGAAGGCTGGG[C/T]ACAGGTGGTGTTGTT | 5336 |
| rs552683578 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865205 | GGTCAGAGCTGGCTG[C/T]CTTGGAAGGGGCTTT | 5336 |
| rs552689189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831579 | CAGTTGGGACCCCTG[G/T]CTGGGTCTCTGACCA | 5336 |
| rs552716110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913584 | AATCTCCAGCCAGAG[A/G]CCTGTGGGCGTCTTT | 5336 |
| rs552721448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854203 | AGAAACAGGGTGAGC[A/G]GAAACCCCAAACTCT | 5336 |
| rs552724820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949935 | GGAGATTTAATGCTA[C/T]ATCTGATGTTAAAGG | 5336 |
| rs552750818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824211 | TGATCTCAGCTCACC[A/G]CAACCTCCACCTCCC | 5336 |
| rs552752784 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909737 | GAATACTAATAACAC[A/G]CAAATAATCCTGGAC | 5336 |
| rs552755115 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777906 | CCTATAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 5336 |
| rs552757212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946481 | GAATGCTGTGTGATT[C/T]TGTGTAGGCAGTGTA | 5336 |
| rs552777972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917963 | CCTGACCTCAAGTGA[G/T]CTGCCTGCCTTGGCC | 5336 |
| rs552786165 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81932017 | AGCAGTCTGGATCCT[C/T]CTGACAGAAAACGTT | 5336 |
| rs552792681 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816128 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 5336 |
| rs552800963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842832 | AAGCTATGAGACGTA[C/T]GGAGGGGCCAAAAGT | 5336 |
| rs552805676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876238 | ATGTTACCCAGGCTA[A/G]GCTTGAACTCCTGGG | 5336 |
| rs552808744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912043 | ACCTCATGATCCACC[C/T]GCCTCAACCTCCCAA | 5336 |
| rs552824329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929015 | CCAGCTCTGCCTCTC[C/T]GTCGCTGTGAGACTA | 5336 |
| rs552831054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820873 | TGATCCGCCCACCTC[A/G]GCCTCCTGAGTAGGT | 5336 |
| rs552838934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847414 | CAGTCTTTAGCCCCT[C/G]TCTCCTTCCTGGACG | 5336 |
| rs552848835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805391 | ATAGTCCCAGCTACT[C/G]AGGAGGCTGAGGCAG | 5336 |
| rs552859664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873601 | ATTTCAAGATGCTGT[A/G]TTGTCAGACAGATGT | 5336 |
| rs552859846 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890885 | TGTATATATGAGGCC[G/T]GGTGCAGTGGCTCAC | 5336 |
| rs552868138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802263 | GATTACAGGCGCCCG[C/T]CACCGCGCCCAGCTA | 5336 |
| rs552870134 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954567 | TTCAACTCCCACTTA[C/T]GAGTGAGAACATATG | 5336 |
| rs552888143 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928721 | TGGCTGACACAGGGT[A/C]CTGTCTTGAATGCCA | 5336 |
| rs552894189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879064 | ACCTCTGCCATTGTC[C/T]GAGCTCCCTGAGTGG | 5336 |
| rs552896760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828002 | GGCTGAGGAAGGAGA[A/T]TTGCTTGCACCTGGG | 5336 |
| rs552922133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922015 | GTAGTGAAGGATGTT[C/T]TGGCGATGAGAACAG | 5336 |
| rs552937859 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885830 | GTAGGCTGATAAATG[C/G]TGAATGAGGATGTTG | 5336 |
| rs552945318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890005 | GCCAGGGAAAGGGTG[A/C]TGCTGATTGGTTGGA | 5336 |
| rs552949634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946076 | ACTGACTTCTCTACC[C/T]TTTGAACTAGGCCTA | 5336 |
| rs552965106 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886058 | CCCTTCATTATTTTC[C/G]TTCCACTAAATTATT | 5336 |
| rs552983127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904268 | CACGTCCCGATTTTA[C/T]GAGACAGATTACTGA | 5336 |
| rs553007993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810752 | ATTCAGTGACTATCT[A/G]TGGATCATTTGCTCA | 5336 |
| rs553011528 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921592 | CCTGTGGTGTTTATA[A/T]ATTCCATTTGGTTCA | 5336 |
| rs553022751 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929456 | GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC | 5336 |
| rs553027328 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820624 | GGGGAAACATTACCC[A/G]ATTTTTTTTTTTTTG | 5336 |
| rs553027971 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777663 | CTTGTGAAGTCACAA[A/T]CGAGTCCTATGGCTT | 5336 |
| rs553030399 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943560 | CACAGAGCCAAACCA[-/T]AACATAGATTTCTTC | 5336 |
| rs553036174 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789200 | AGCTCATTGTGATGG[A/G]CATGAGACAGGATTT | 5336 |
| rs553070284 | in-del | -/TTTTTT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816676 | TTTTTTTTTTTTTTT[-/TTTTTT]AGTAGAGGTGGGATC | 5336 |
| rs553082271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873328 | ACAACCACAACAAAA[A/G]CCATGATTCATAAAA | 5336 |
| rs553088140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900293 | TCATCTTTTCTGTAG[A/G]TTTGAACTTGAAAAA | 5336 |
| rs553108012 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862257 | AGCCCGGGCAATGGA[C/G]AAGTCTTAGGTGTTT | 5336 |
| rs553108452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798419 | GTTAAGTGCTCTTGG[A/G]CCTGAGCCTGGATAT | 5336 |
| rs553113996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888966 | GAGCCCAAAATATTT[A/C]CCTCTGGCTCTCTGC | 5336 |
| rs553120194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838856 | TGGTGCATGTAAGGC[C/T]CAAGGCTTTAAGCAT | 5336 |
| rs553124586 | snp | C/T | 0.000189735 | 0.00973815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897848 | CCGTGCCCAACCCGA[C/T]TGGTTATTTTTATTG | 5336 |
| rs553131341 | in-del | -/TT | 0.131038 | 0.219882 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821871 | GACAGATCCAAGATG[-/TT]TTTTTTTTTTTTTCC | 5336 |
| rs553141701 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836365 | TTCCCACTGGTGGAG[C/G]CAAGAGGTTTTTGCT | 5336 |
| rs553143587 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832114 | AAATGGAGGGGGGGA[A/G]TAGTGATATTGTGGC | 5336 |
| rs553150396 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887809 | TCATCCCCTTTTCCT[A/T]TGAATATTTGGGATT | 5336 |
| rs553155091 | in-del | -/GCGGG | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957587 | GGCATGTAATGGGGT[-/GCGGG]GCGGCCGGGGTTGCC | 5336 |
| rs553166922 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851130 | TTAGAGATACCACCC[C/G]CCTAATAATAGGGCC | 5336 |
| rs553169902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802018 | TCCAAAAAATCTGTG[C/G]CTGTGCAGAGGTGCC | 5336 |
| rs553171080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863327 | GTATCTGGCTTATTT[A/C]ACTTAGTGTAATGTC | 5336 |
| rs553173600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954165 | ATAGCTGGGAGTACA[C/G]GGTATGCCACCATGC | 5336 |
| rs553184218 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958257 | TTTTGGCCTCTCATG[G/T]TCCAAACCTCATTGA | 5336 |
| rs553200360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827799 | CTCATTTAAAAAAAA[C/G]CGTTGACGCCGCCAG | 5336 |
| rs553203069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836109 | ACTTTCTTTCCAGGG[C/T]CACCAAGGACAAGAC | 5336 |
| rs553206284 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932745 | GTCCATGGGTGCCCT[C/T]GCTGGTGGGGCATCG | 5336 |
| rs553207908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901474 | GTGACTCAGGGACCC[A/G]GGGCCCCCGCATTCT | 5336 |
| rs553211815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820651 | TTTGAGACAGAGTCT[C/T]ACTCTATTACCCAGG | 5336 |
| rs553219731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898222 | TGGAATCATCTAACA[C/G]CTATAGGGCTAGAAC | 5336 |
| rs553237933 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962066 | AGCTGCGCGCTCCGT[C/T]GAAGAGGACGACCAA | 5336 |
| rs553253157 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850866 | ATCTCCTGCACATGC[A/G]GGCAATAGGGTTAAC | 5336 |
| rs553258339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886232 | TCCCCAAACGGGGCC[C/T]TTTGCTGGGCTGCCC | 5336 |
| rs553265882 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81840811 | GAGGCAGCTCCCTTC[C/T]GAGTGGCAAGGAACA | 5336 |
| rs553270575 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854126 | AATAGTCTGTGCTTA[A/T]TTCCTGAAATCTCAG | 5336 |
| rs553270784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905304 | CAAGAACAGGCAGTG[C/T]AAAGGCCCTGCCTGG | 5336 |
| rs553282280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812960 | TGCTTGTTTTTGTCA[A/C]GTTTGTCAAAGATCA | 5336 |
| rs553292130 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805875 | AAACTCCTGGGCTCA[A/G]GTGATCCTCCCAGCT | 5336 |
| rs553293443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782575 | AGGGATCTTTTGGCC[A/G]TGAAGATCTGTTTCC | 5336 |
| rs553302398 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827864 | GGGAGGCCAAGGTGG[A/G]TGGATCACCTGAGGT | 5336 |
| rs553303850 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938378 | AGGTTAAGGGCGGGC[C/G]GGTGGTAGGGGGAAG | 5336 |
| rs553314444 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961766 | ATTTAAAAAGTAATA[A/C]AACAGTTTTATTTAA | 5336 |
| rs553342998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781788 | TCCTGTACTGGCTTA[C/G]CATGCACAGAGCACT | 5336 |
| rs553345557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816725 | TAGGCTGGTCTTAAA[C/T]TCCTGGGCTAAAGCA | 5336 |
| rs553346755 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81790997 | TGTTTGCTTTGCTCA[C/T]AGCAATAAAATGTCA | 5336 |
| rs553356083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947964 | TACAGGTGCCCTTTT[C/T]TACTTCACAGACGAC | 5336 |
| rs553366136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843501 | GAAACACCCCAGCCA[A/G]TTTCCTTAGTATCAC | 5336 |
| rs553378189 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950630 | GTTAGAAAACTTTAA[C/T]ACATTTTTTAAAAAT | 5336 |
| rs553379486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813247 | ATAGCATTGAATCTA[C/T]AAATTACTTTGGGCA | 5336 |
| rs553386753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891392 | CTGTTCTTCCCCCCT[A/G]GTGGGCGCAGACCAG | 5336 |
| rs553387600 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917765 | CTTGCTCTGTTGCCC[A/C]GGCTGGAGTGCAGTG | 5336 |
| rs553392230 | in-del | -/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81926314 | GTGGTGTGGTCAGAG[-/GT]GCATTTTGGAGAGTC | 5336 |
| rs553409812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865924 | AGCTCCACTGGGGCA[A/C]CAGCATGAGAGGACG | 5336 |
| rs553416414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942606 | GCCTTTATTGTGTTA[C/G]GTACCTTAAACTCTT | 5336 |
| rs553427167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869605 | ACTGCAGCCCATTTT[C/T]TCCCTAGTGAAATGA | 5336 |
| rs553436115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822528 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 5336 |
| rs553438673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917725 | TTGTCCATTTTTTAA[A/C]ATTTTTTATTTTTTG | 5336 |
| rs553443762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921703 | TTTACTTTCAGCCCT[C/T]GGCTCCTCCTTGCCA | 5336 |
| rs553449657 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889607 | ATTACTCAAATCATC[C/T]TCCCTTTCAGAGGCT | 5336 |
| rs553457034 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81903422 | AAGAGCATCAGTGCA[C/T]GGGGAGTGTTTGGCC | 5336 |
| rs553468668 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871215 | AATTTGATCTGAGTC[C/T]GTTAAAAAAGTGCAA | 5336 |
| rs553494835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810246 | ATGCCTCAGCCTTCC[A/G]AAGTGCTGGGATTAC | 5336 |
| rs553501978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917335 | TCTACACCTTGGCTA[C/T]GGTGAATGGTGCTAT | 5336 |
| rs553529198 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838009 | CATAGTCAAGAGACT[-/A]AAGCAATGTAATGAT | 5336 |
| rs553544224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834122 | CTTTGGCATCAAAAC[C/T]CAGCCAGGTGGCCTT | 5336 |
| rs553544358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838105 | TTTTTTTGAGGCGGA[C/G]TCTGGCTCTGTTGCC | 5336 |
| rs553556864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934076 | GAAGAACTAGAATTT[A/G]AGACACTCTAACAGT | 5336 |
| rs553559401 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81938316 | AGAAAGTGTTGTTGC[C/T]TTGTAAGAATTTTTG | 5336 |
| rs553593547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906888 | ATTAAAACTACAAAA[A/C]TAAGTTGGGCATGGT | 5336 |
| rs553605532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837855 | CCTGTAGTGCAGTAT[C/G]ACAGCCAGGATATTA | 5336 |
| rs553608675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895545 | AGCCTGGGCAACAGA[C/G]CGAGACTCTGTCTTA | 5336 |
| rs553609504 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892223 | AGGGGAGGAAGGCAG[A/G]TCCTGCTGGAGCAGG | 5336 |
| rs553655567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937972 | TGGGCCGATGCTGTC[C/T]TGAGAGCAGGGAACC | 5336 |
| rs553656164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913738 | TGGCAGCTACTGTGG[A/G]GTGTGTGGTTTGCCC | 5336 |
| rs553656501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856259 | ATAAAGTACCTGGTG[C/T]TTAAGGAGAGGCTTC | 5336 |
| rs553657822 | snp | C/T | 0.000252979 | 0.0112439 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786172 | GACCGCTGACAAGAT[C/T]GAGGGCTTCTGTGAG | 5336 |
| rs553668956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881074 | CCAAAGGGGCAGGGG[A/G]CCCCTGCTGGGGAAT | 5336 |
| rs553690490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818633 | ATAGCCAGGACAGAG[C/T]CAACTAGCCGGGCAT | 5336 |
| rs553723083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845754 | GATGCCCCTGCCTGA[C/T]GTAAGATCAAGGGGT | 5336 |
| rs553725536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913325 | CTGCTATATGTTGAG[C/T]TCCTAACCGTGTTCT | 5336 |
| rs553732074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791212 | CATAGCAGGAGTTTT[C/T]ACTGGATGTGGTGTG | 5336 |
| rs553739114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900513 | CCCCGAGCAGCGCCC[A/G]GTTTCTGTCGTCCCA | 5336 |
| rs553751246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903735 | CTGGTTGCATGTGCT[C/G]TTCCCTGTTCCCAGC | 5336 |
| rs553783117 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829635 | TTCTCCTCGTATGTT[-/CTC]CTTCTGTTCCAGGAT | 5336 |
| rs553785727 | in-del | -/TG | 0.499583 | 0.0144353 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884603 | AATTGTATGGATCTG[-/TG]TGTGTGTGTGTGTGT | 5336 |
| rs553793914 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81894956 | GTTACCAAAACGACT[A/C]ATCATGGAAGCAACG | 5336 |
| rs553795046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796909 | GGCAGGCCTAACACA[C/T]AAATACACTCTCATG | 5336 |
| rs553800109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853223 | GTAATCCCAGCTACT[C/T]CTGAGGCTCAGGCAG | 5336 |
| rs553816673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903398 | GGGGATGTTGGTGCC[C/T]CCATGGGTAAGAGCA | 5336 |
| rs553820741 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960895 | CATCTTCCTGTTATA[C/T]TCTTCTCTAAGATTC | 5336 |
| rs553824802 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780765 | GGCACGGTGGCTCAC[A/C]CCTGTAATCCCAGCA | 5336 |
| rs553840611 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896534 | AGTGAGGTCACATTG[C/T]GCCACTGCACTGCAG | 5336 |
| rs553849920 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800216 | TATTGTTTAAATTTA[C/G]TTTTATTGTAAGTTC | 5336 |
| rs553858025 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899733 | AGGCTGTGATGTGCC[C/G]GATGGAGAAAACACC | 5336 |
| rs553882011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954142 | ATCTTACCCTCTCAG[C/T]CTCCTGAATAGCTGG | 5336 |
| rs553882455 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799238 | AGCCCCCGCCACCCC[A/C]CTACCCAGAGAGATG | 5336 |
| rs553882860 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900021 | TAAGAAAAATCAACT[A/G]CAGATACACACAAAT | 5336 |
| rs553886384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780323 | CCAGGGCTGTGTCGA[C/G]AATTGGGGCTTATTG | 5336 |
| rs553894956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919330 | CATCATTGTTTTCTT[A/C]TTGTCTTGTATTCCA | 5336 |
| rs553916666 | in-del | -/T | 0.00118387 | 0.0243008 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880882 | ACTTGTCTAAGGTTC[-/T]TTTTTTTGTGTGTGC | 5336 |
| rs553923895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848818 | AAAGGAGGGCTGTGG[A/T]TCCACAGATTCCATC | 5336 |
| rs553928771 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957013 | CCGGGCATGGTGGCT[C/T]ACAGGCCAGGCATGG | 5336 |
| rs553932622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784532 | TCCTGGGAGGGTCTC[C/T]CTAGTGCTACTCTGT | 5336 |
| rs553943389 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955679 | GCAACGTGGCCATGA[C/G]AGGACCACACTTACT | 5336 |
| rs553948753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940135 | CTGGCTTCAAAAAGA[A/G]TGAAAAATGATTTTT | 5336 |
| rs553950127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927980 | TACCTGGTGCAGGGG[C/G]TGGGGTTTGGGGTGG | 5336 |
| rs553968457 | snp | C/G | 1.65877e-05 | 0.00287986 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869180 | GCTGTTGAAAACCCT[C/G]AAGGTGACAGAACTG | 5336 |
| rs553972025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916487 | TGACAAATAAAAGTT[A/G]TTTATATGTATCATG | 5336 |
| rs553973165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807854 | AAGAGAGAGAGGGAG[A/G]GAGGTGCCACATACT | 5336 |
| rs553979280 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81818023 | TGTCATCTACTCTCT[C/G]TTCCTTCCTTTCATG | 5336 |
| rs554017986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864707 | GTTGCTACAAAAGAG[C/T]CGGGGGCAGTGGAGG | 5336 |
| rs554024140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935773 | TTGGCAGGTGATTCT[A/C]AGTTTGTTCATCTTG | 5336 |
| rs554032702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920661 | AAGGTGACATGAGGA[A/G]CAGAAAGAAGAGTTA | 5336 |
| rs554041631 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841628 | AGATGAGAAAATAGA[A/C]AGTAAGCCAGAATAG | 5336 |
| rs554044639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811203 | CTGTCTGTGTGACTC[C/T]CTCCTTGGGTCTCAG | 5336 |
| rs554058543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915656 | GAATAAGCTAATAGA[C/T]GATGATCCTAATGCT | 5336 |
| rs554063847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944209 | TGTATACATAAATAA[A/G]ATGGATTGATGGGTA | 5336 |
| rs554070989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893224 | GTGCATTAAAGAGTC[A/G]TTCTTACGGCAGTTT | 5336 |
| rs554083358 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941646 | GAGTATTCATTTGTA[A/G]GAGGCCTGATATTTG | 5336 |
| rs554105217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864334 | GTGGCCATTTCAACA[A/G]AACAAAACAAAATGA | 5336 |
| rs554110947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928301 | AGCATTATGAAACCT[A/G]TTCTAGAATTCACAA | 5336 |
| rs554112632 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934279 | AACGAGAGGGGCAGG[-/T]GTTGTCTTCAGGAAA | 5336 |
| rs554112913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801167 | AGTAGCGTAGCGATT[C/G]AGAATAAATAACCCC | 5336 |
| rs554120705 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813029 | GTTCTGTTGCAATGG[A/T]CTGTATATCTATTTT | 5336 |
| rs554139771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826978 | GACTGAAGATAGGAC[A/G]CTTGATCCTGGACTT | 5336 |
| rs554153487 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810796 | TATTGAGTTCTGATA[G/T]AAGGAGACAGGGTCT | 5336 |
| rs554157647 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815193 | TGCAGAGGGTGGTTA[G/T]GCGAAGGGAGGAGGT | 5336 |
| rs554178543 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957329 | AACAAACAAAAAATC[A/C]TTTGGCACCCTTGAC | 5336 |
| rs554199954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872022 | GGAGTCAGGTCTGCT[A/G]TTTTGTTAAAAATCA | 5336 |
| rs554214414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827254 | TGCAGTGGTGCCACT[A/G]TCGCTCACTGCAGCC | 5336 |
| rs554220536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811278 | GTGTGGGTGTAAAGA[C/G]TAGAGATCGGGTATG | 5336 |
| rs554220681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818644 | AGAGCCAACTAGCCG[G/T]GCATACCTTTTCTCT | 5336 |
| rs554237118 | snp | C/T | 9.93822e-05 | 0.00704849 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81919589 | GCTCGTCAGTTACTA[C/T]GAGAAGCATTCACTC | 5336 |
| rs554238785 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823233 | GTCTGGCTTCCCCGG[A/G]GCTTTACCTCGAGAC | 5336 |
| rs554318321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872608 | CACCTAGCACAGTAC[C/T]TGGTAGGTGGCACAC | 5336 |
| rs554320587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797329 | CTAGTCTGTCTTAGA[C/T]ATAAATGCGGGTTTT | 5336 |
| rs554329291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957443 | GAAGGACACTTCAAT[A/T]TAATAGCGAAAATAA | 5336 |
| rs554346390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931715 | GGCTTTGGTGCTCAG[C/T]TGGGACTGTGGGTGG | 5336 |
| rs554359233 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868001 | ACCACCGTGCCTGGC[C/G]CTCGCTTCCCGCTTC | 5336 |
| rs554363067 | snp | A/G | 4.968e-05 | 0.00498373 | missense | PLCG2 | GRCh38.p7 | 16:81858346 | GCGTCCACGCCCACC[A/G]TTATCGAGAGGTAGT | 5336 |
| rs554367908 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799269 | GTGTTAACACCTGGT[A/G]TACCACCTTCCAAAT | 5336 |
| rs554369937 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960961 | AAAGAAAATATGGCT[A/G]TCTCCACCTCTAGTC | 5336 |
| rs554389785 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81883012 | CTGGGGTGCACCAGA[C/G]CTATTTTGGAGCAGC | 5336 |
| rs554394342 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834443 | GGCAGGACTCAGACC[C/G/T]CAGCTTGCCCAACCT | 5336 |
| rs554399590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945186 | TTGTTTGAAGGTGAT[A/G]AAGCAACTGAGAGTA | 5336 |
| rs554401344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872539 | CATGTTACCTTTGCA[A/G]TAAAAAGTTCCATAG | 5336 |
| rs554403762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830569 | GGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 5336 |
| rs554405906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888770 | AACAAACGTAAAGAG[C/G]TATCATAGGGCAGGA | 5336 |
| rs554414948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885167 | AAGTAGCTGGGATTG[C/T]AGGCGTCTGCCACAA | 5336 |
| rs554430239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819623 | CAAGCTTCGCTCTTT[C/T]GCCCAGGCTGTAGTG | 5336 |
| rs554448088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924839 | CCCTTGGAGGCTCCC[A/G]GACCCAGTTGGGCAA | 5336 |
| rs554460161 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860321 | CTGCTCCCAATCCTT[C/T]ATCATTACTGTGATT | 5336 |
| rs554472252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940493 | GAGGGTCCAACTCCC[C/T]AAACCCTTCAGAATT | 5336 |
| rs554473327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948900 | ATAGATGGCTGGCAG[C/T]TGAAACTGAGCCAGT | 5336 |
| rs554473705 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785324 | GAGGCACAGAGAGGT[C/T]AAGCAGTCTACCCAG | 5336 |
| rs554491482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823724 | CTGTAGAGACAGGGT[C/T]TCTCTATGTTGCCCA | 5336 |
| rs554491621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819314 | CAGGTGTGGAGTGAC[A/T]ACACTGCCTCATATC | 5336 |
| rs554514527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903508 | TGTCTTAGTCTTGCA[G/T]ATGAGAAGTGTGAGG | 5336 |
| rs554518833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838722 | ATGGCACAGGTATGC[C/T]TATGTAACAAACCTG | 5336 |
| rs554531352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846642 | CTTAAAAAGATCATG[A/T]GTAGATAGTCCATGT | 5336 |
| rs554545661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827671 | GGGAACCGTGGTTAA[C/T]GGGGAGTCAGTGCAT | 5336 |
| rs554547154 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865062 | GGGGAAGGAAGGCAG[C/G]TGGAACAGGCAGCTG | 5336 |
| rs554593546 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912088 | AGGCGTGAGCCACCA[C/T]GCCTGGCCCAATTTT | 5336 |
| rs554596146 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788751 | TTTTGGAGCCCAGTG[G/T]GTCTCTTGTGGCACA | 5336 |
| rs554613246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900555 | TGGCCCCTCTGTGGG[G/T]CAGATGCAGAGGTGT | 5336 |
| rs554623028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892904 | CCAGGCTGGAGTGCA[G/T]TGGTGCGATCTCAGC | 5336 |
| rs554638651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920710 | GTGGGGGTGGATCTT[A/G]TCAGTGGTGTGCTAG | 5336 |
| rs554641423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915698 | GGGTTGTGGATCCCC[A/G]ATGCTGTGGATCGGG | 5336 |
| rs554646625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920075 | TGAGGTAGAAGCCTG[C/G]CTGGAGGCACCAAGA | 5336 |
| rs554661858 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896906 | TTCATTTCAAGGGTT[G/T]CTGACCTCAGGTGTA | 5336 |
| rs554664974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796948 | GCCTGAGGGCAACGG[A/G]GTGAGTACAGGGATT | 5336 |
| rs554668565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830939 | GAGGGTTTCAGAGAG[C/T]ATACGCAGTGTGTCC | 5336 |
| rs554672809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839553 | ATTTTATATCTAATA[C/T]TTATTTTAATATTGA | 5336 |
| rs554673408 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81929536 | GAGTAGCCGGGACTA[C/T]AGGCATGGGCCACCG | 5336 |
| rs554675797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948939 | CAGATGATGAGAACT[C/G]TAACACATAACTCAT | 5336 |
| rs554688035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876197 | TGCAGGCTAATTTTT[C/G]TATTTTTTGTAGAGA | 5336 |
| rs554692221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853781 | TATAAGGCATAAATA[C/G]TGGAGGCTGTGGCCC | 5336 |
| rs554703658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932144 | GGGAGTGACCTTTTC[A/G]GGGCTGTCCTACCTG | 5336 |
| rs554707162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861380 | GTTACTTGTTAGCTT[C/G]AGGGTTTGGGTGAGC | 5336 |
| rs554725113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896381 | ACACACACACACACA[C/G]ACACACACACACACA | 5336 |
| rs554728719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878993 | AGTTGCAAGACCTGG[C/T]AGAGGAGGGGAAGCC | 5336 |
| rs554738147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790062 | CTCTGAACTTTAATT[A/C]CCTTATCTGTGGACT | 5336 |
| rs554740964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953254 | CAGGAAAAGGAGACT[A/G]GTGGAAAACCCAGTG | 5336 |
| rs554753075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902727 | TTACCCATTCTCACA[C/T]TGCTCATAAAGACAT | 5336 |
| rs554759606 | in-del | -/CTC | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958234 | ATTCCCCAAAATGTG[-/CTC]CTCATTTTTGGCCTC | 5336 |
| rs554771601 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805514 | GAAAAAAAAAAAAAA[-/C]AAAACAAAACGCAAG | 5336 |
| rs554793625 | snp | C/T | 3.31763e-05 | 0.00407272 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81907705 | GACTCGGCACTACTG[C/T]GCCATTGCCGATGCC | 5336 |
| rs554794389 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825496 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 5336 |
| rs554803464 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886213 | TTGACTTTATTACGT[A/G]CTTTCCCCAAACGGG | 5336 |
| rs554805335 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842917 | GCTGGAGTGGGGTGC[C/T]GGCCTTTGAGGCTGA | 5336 |
| rs554818064 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785023 | CTTCTGGCTCTGCAT[A/C/T]TGAGAATTGACCCTA | 5336 |
| rs554837780 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884458 | AAACTCTGTGAGAGT[C/G]AGATCAACTTGAAAT | 5336 |
| rs554838585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811594 | CTCATTGTTCAACTC[A/G]CACTTAAGAGTAAGA | 5336 |
| rs554847882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860769 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 5336 |
| rs554866020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911907 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 5336 |
| rs554884692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860348 | GATTAATGCTGCTGT[A/G]GAAACCTTTGGGTCT | 5336 |
| rs554896521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917127 | CCTTTTTAGGTTTCA[C/T]GTATGAGATCCTGTG | 5336 |
| rs554902941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847917 | AACCGATCCCCAACA[C/G]TCACTGAGGGATGAC | 5336 |
| rs554923149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794197 | CCTGGAAAAGGGCTG[C/T]TGGGGACAAGGGTGC | 5336 |
| rs554933911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797843 | TTTTCTTGTCTTTTT[C/T]TTTTTTGAGATGGAG | 5336 |
| rs554936152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899045 | ATACAAAAAATTAAC[A/T]GGGCATGCTGGCAGA | 5336 |
| rs554936328 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961921 | AAATGTTAAGATTGC[G/T]GATCGGATGTGAGGG | 5336 |
| rs554954017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823771 | CTGGCCTCAAGCAAT[C/G]CCCTGACCTCGGTGT | 5336 |
| rs554960283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953653 | CCAGGAAATAAGTAT[C/T]ACAAAATGCTTTCTC | 5336 |
| rs554974884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925224 | GGCTGTGGTCAATTC[C/T]TCTCTCTGATGGCAG | 5336 |
| rs554976452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850291 | TTTTGAGATAAATTA[A/T]GTATTTTGGGGTGCA | 5336 |
| rs554985855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798195 | CCATCAGATCACTGG[A/G]AGGATTCAGTTTGTA | 5336 |
| rs554988675 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890739 | CAGATCGCTAAAGCA[A/T]TTTTTTTTAAGGGGC | 5336 |
| rs555011601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902181 | GTGGAATCTGAAGTC[C/T]CTAGCGGGGCAGCCT | 5336 |
| rs555011871 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945146 | CCTCTTCATAAGCAG[C/T]GGAAAGTGAGAGATT | 5336 |
| rs555017050 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930783 | TTTAAATTATTTATT[C/G]TTTATATGTAAAAGA | 5336 |
| rs555036869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926639 | GAAGCACTCACGTTT[A/T]TGCATTTTTCAGATG | 5336 |
| rs555040817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799571 | CTGGGATTACAGGTG[C/G]AAGCCACTGAGCCTG | 5336 |
| rs555057145 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959082 | TACATACCAATAATG[C/T]AATATGGCTTTTTAA | 5336 |
| rs555060754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875779 | TCAAAAAGAAAATTG[A/G]GAAGGCTGCTAACGT | 5336 |
| rs555071780 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832663 | CCTGCCTCAGCCTCC[C/G]TTAGTGCTGGGATTA | 5336 |
| rs555074154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825243 | GTTTTTTTCCTATTA[C/T]TGCTCTAATCTTTTA | 5336 |
| rs555075643 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81947394 | TCACCTGGTTCTGTG[A/C]CACTCACAGGTGCAG | 5336 |
| rs555099128 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812375 | GACTTTTTAATGATC[A/G]TCATTCTAACTGGCA | 5336 |
| rs555107012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955640 | CCTCTTTTTCTGGCA[C/T]ATTCCAAACTTCTTG | 5336 |
| rs555111650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826911 | GGTCTTGGTTTATCC[A/C]TGCTGGAGATCCGCA | 5336 |
| rs555114066 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856882 | GGGAAGGTCATTCCC[A/G]GAGAAAGAGATGTGA | 5336 |
| rs555132203 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844586 | CTAGGCCTCCCAAAT[C/T]GCTGGGATTACCGGC | 5336 |
| rs555134803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791986 | TCACTTGCACCAACT[C/T]AGATCAGCAAGCCCA | 5336 |
| rs555137127 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81948611 | TTTAGAATCCTGGAG[A/G]TCCAGGACTGGGAGC | 5336 |
| rs555146356 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865581 | TGCTCTGGCACCCCA[C/G]GCCCCTCAGTCTCTC | 5336 |
| rs555153836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855068 | TACAAAAACTAGCTG[A/G]GTGTGGTGGTGCGCA | 5336 |
| rs555155047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816543 | AGTGCCATGGTGCAA[C/T]CACAGCTCAACTACT | 5336 |
| rs555193690 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885574 | GCAAACCCCAGACTT[A/T]GCGTCATTTTGTTTG | 5336 |
| rs555215253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879993 | GCCTGTAATCCCAGC[A/T]ACTGAGGGGGCTCAG | 5336 |
| rs555238482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916848 | TCACCATGTTGGCCA[C/G]GCTGGTATCGAACTG | 5336 |
| rs555259463 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795698 | TGTTTCCTCCCACCT[C/G]CTTTTTTTTTTTCTC | 5336 |
| rs555262707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893277 | AGCCGATTGCACCAA[A/C]AGTTGTTGAATATCT | 5336 |
| rs555263865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848373 | GGCTGGCTTCCAAAG[G/T]GTGCTTGTTTGGGCC | 5336 |
| rs555264841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793883 | GCAGAGCTACAATTT[C/G]AACTTGTTCTTCCCA | 5336 |
| rs555267708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844382 | GTGCAGTGGTGTGAT[A/C]TTGGCTCACTGCAAC | 5336 |
| rs555273190 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951175 | GTGTGGAGACAGGGC[A/C]CTGCTTTGCTGCCTA | 5336 |
| rs555281691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820084 | TTCATCTTTAAGGAT[G/T]ATGATCTTTTAGGTA | 5336 |
| rs555287006 | snp | A/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962558 | TTAATTTATTTTTTA[A/T]ATAAATAGTATGTGC | 5336 |
| rs555315238 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916290 | TGGAAATCCTTTTTT[-/A]AAAAAAGAAAAAAAA | 5336 |
| rs555315724 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922745 | GGAAGCTGCTCATTT[A/C/T]AACAGGTTTGACAAC | 5336 |
| rs555336722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872923 | GAGCTGTGGGCTGGC[C/T]ACACAGTGAGGCCAC | 5336 |
| rs555342788 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800832 | ATCTTGAGATGGGGA[G/T]ATGATCCTGGATTAT | 5336 |
| rs555345075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819660 | CGCTATCTCGGCTCA[C/T]TGCAACCTCCGCCTT | 5336 |
| rs555360837 | snp | C/G | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963165 | TAGCCTATGACAAAC[C/G]TCTGCATTAGAAGAT | 5336 |
| rs555375075 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875274 | CAACCTGCTCTATGT[A/G]TTTTGTATACATTTA | 5336 |
| rs555381328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950914 | ACAAAGGAATAAAAG[A/G]GATAGAAACCAACTG | 5336 |
| rs555399772 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823844 | AATTCTTTTCTTTTC[-/T]TTTTTTTTCCTTCCT | 5336 |
| rs555407542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788131 | AGTTTCATCATTTTA[C/G]GAACTGTCAGACTGT | 5336 |
| rs555420818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877433 | GCACTCCAGCCTGGG[C/T]GACACAGCGAGACTC | 5336 |
| rs555424549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874127 | TAATGGTTTAAATAT[A/G]TTAAAAATTAATTGC | 5336 |
| rs555426318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926429 | CTTAGAGGTGCTCAC[C/T]GTCTGGTGGGGTCCA | 5336 |
| rs555429252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855858 | GATGTAGGAAATGAG[C/G]AGCGAATGTCTGACT | 5336 |
| rs555441335 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803037 | CCCCATCCCTGGCAA[C/T]GACAAATCTACTTTT | 5336 |
| rs555442516 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802615 | TTCACTCTTGTCGCC[C/G]GGCTGGAGTGCAGTG | 5336 |
| rs555464015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880594 | AAATTGTGAGATGTA[C/T]GTAAATGTTATAATA | 5336 |
| rs555465029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914788 | GGGATGTAGTTGGTG[G/T]TTGGTGAATGCTGGC | 5336 |
| rs555479598 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805076 | CAACATCAGACACTT[A/T]TCCCCAATCACCATG | 5336 |
| rs555482383 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817455 | CACGCTGGAGTGCAT[C/T]GTCTTGAGGGGTGCT | 5336 |
| rs555494581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935215 | AGCCATTCCCTTCTT[C/T]CAGTTTCTGGGGGCT | 5336 |
| rs555502652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806549 | GCTCAGCTTGTGGCC[A/G]GGGAGCTTCATGACC | 5336 |
| rs555516982 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853006 | TGGCTTCCCCCAGAG[A/C]ACAAAATGGAAGGTA | 5336 |
| rs555518176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948001 | TGATTTTCAAAGCCA[C/T]TGATGCCTGTTTCAT | 5336 |
| rs555518235 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81791681 | GCTATTCTCCCACCT[C/T]AGCCCCCCGAGTAGC | 5336 |
| rs555523542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906252 | CGTGCATTTAGGTTG[C/T]CCTGACTCCTTCGTG | 5336 |
| rs555537579 | snp | C/G | 1.66785e-05 | 0.00288773 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910706 | GCCCAACCCCAACCC[C/G]CACGAGTCCAAGCCG | 5336 |
| rs555561680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875048 | GATTCACTGCAACCT[A/C]TTCCTTCCGGGTTCA | 5336 |
| rs555588521 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804268 | GTGAAGTGTTATGTC[A/T]TTGTGGTTCTGATTT | 5336 |
| rs555591310 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795968 | AGGGCCTAAGTTGGG[G/T]GGCATCCTTCCAGGC | 5336 |
| rs555594880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836918 | GCTGTGCACACGGGC[A/G]TGTACTCAGTGTTTC | 5336 |
| rs555595799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887121 | CCAGGCAAAGTTGTT[G/T]TTTTTTTTTTTCTTT | 5336 |
| rs555602210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947442 | CACTGGGATGAAGAG[G/T]CGCTCTTGGAAGCCG | 5336 |
| rs555605832 | in-del | -/TTGT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919431 | GGGTTTGTGTAAAAA[-/TTGT]TTGGCCACCAGGATC | 5336 |
| rs555606073 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943090 | AGCCTGGAACCATGC[A/T]ATTGGAGTGTAGGGG | 5336 |
| rs555612476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817883 | CCCTGTGCTTATGAA[C/T]ATGTTCTCACGTTCC | 5336 |
| rs555624026 | snp | C/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944549 | AGCTCATGGCAGCCT[C/G/T]AGACTCCTGGGCTCA | 5336 |
| rs555641853 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846922 | CGCATCAAGCAAACA[A/G]TTCTCCATTGGACAC | 5336 |
| rs555648688 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799829 | CGATCTCCTGACCTC[A/C/G]TGATCCTCCCACCTT | 5336 |
| rs555651826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803907 | AGCTAGTCTTGAACT[C/G]CTGGCCTCAAGTGAT | 5336 |
| rs555651833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807720 | AAGACTGGGTAATAT[A/C]AAAAGGAAAGAGGTT | 5336 |
| rs555665409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947121 | CAAGGCTGTTGTAAA[C/G]AACCGGAAACATTAT | 5336 |
| rs555667043 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870581 | TGTGAGTATGTTTTC[C/G]CAGACAGGGGGATTA | 5336 |
| rs555688393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822597 | CCCCGTCTCCACTAA[A/G]AGTGCAAAAATTAAC | 5336 |
| rs555691486 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842036 | ATTTCATGTTATTTC[A/T]TTTGGTTTGCATGAC | 5336 |
| rs555693167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895509 | AGATTGCAATGGGCC[A/G]AGATTGTGCCACTGC | 5336 |
| rs555731607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800352 | GCTATTTATTCTGAT[G/T]CTCTCCTCCATCCTT | 5336 |
| rs555731857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844794 | TATGTACATGTACAC[A/G]TGGCCATGTATGTGT | 5336 |
| rs555747668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826298 | AAGGCTCCAGGATCC[C/T]AGGCTCAGAGATGGG | 5336 |
| rs555748446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899418 | GGTGATCCTTATTGG[C/T]GGATTCTACTTGCTA | 5336 |
| rs555757587 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810888 | TGTACATGACTATAT[G/T]TATAACGAAAATGAA | 5336 |
| rs555763825 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780242 | TTCCATCAGTGGGAC[A/C]CTGGGCAAGTTGAAG | 5336 |
| rs555783855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837221 | TCAGAAAAGTGTGTG[A/T]TCAAATGAAAGGCTG | 5336 |
| rs555785628 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960114 | AAACTGTCTCCTTCT[C/T]CTGGTGCTACAACCG | 5336 |
| rs555811782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899130 | GGAGGCGGAGGTTGC[A/G]ATGAGCTGAGGTCAC | 5336 |
| rs555813507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956071 | CCACTCACTCCATCC[C/G]CCAGACCCCGGTGAC | 5336 |
| rs555818662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814599 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 5336 |
| rs555824211 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959825 | AACCCCTCTCAGCTC[C/T]GTTAGGACTTCCACA | 5336 |
| rs555841491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841293 | CTAGGCTGGAGTGCA[G/T]TGGCATGATCTTGGC | 5336 |
| rs555844846 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889888 | GTCGACTTCCTGACC[C/T]TTGTGATCAGCCCGC | 5336 |
| rs555850920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833228 | ATCACCCTTTAAAGA[A/T]GGAGTGCTTTACCTT | 5336 |
| rs555856392 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847662 | TTAAGCTATGGTCGA[C/T]TGAAAATATTTGAGA | 5336 |
| rs555859202 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890782 | CTTGAAATTTCCTGC[C/T]CTTTCAACATTCTGA | 5336 |
| rs555886166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947472 | GAGCTGAATTGCATT[C/T]GGTAGACCTGGGCTT | 5336 |
| rs555898228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951642 | CTAACCTCATTCAGC[C/T]GTAGACCAATGTCAT | 5336 |
| rs555904146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887455 | CACAATTTGGGTTTC[A/G]TGTTCTAGTATTCAA | 5336 |
| rs555917741 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841584 | TTCAGATATATCTCT[A/G]TAGGGTGTATGTTCT | 5336 |
| rs555918609 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878004 | TTTTTTTTTTTGAGA[C/G]GGAGTCTCGCTCTGT | 5336 |
| rs555937357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874491 | CTCACTGCTGTTGTG[C/T]AGGTAAATGCCCATC | 5336 |
| rs555955985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852671 | TTGTTTCTGTTATCT[A/C]TTGCTATACAACAAA | 5336 |
| rs555957389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849296 | GGCTTGGATTGTGGT[A/G]TTGGCCATGGAAATG | 5336 |
| rs555962370 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81867455 | GGTTGGAGTTTGAGG[C/T]TAGCACAGATAAGGT | 5336 |
| rs555975146 | snp | C/T | 0.000101295 | 0.00711598 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910752 | GGAGCAGGAGGCAGG[C/T]GGTGGTCGGGTTAGC | 5336 |
| rs555981764 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799756 | CGCCACCACACTTGG[C/G]TAATTTTTTTGTATT | 5336 |
| rs555989210 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893490 | TGGTCAGCAGTCACT[G/T]CCTGCGATTGTGGCC | 5336 |
| rs556002209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899778 | TTGGTTCAGGCACGA[A/G]TTACAGTGATGCTGG | 5336 |
| rs556002304 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951233 | CCTCCCCAAGTGCTG[A/G]AATTACACGTGTCAG | 5336 |
| rs556004523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852025 | TCACCTCTGGACTTC[G/T]TTCTGTCCTCTTCCT | 5336 |
| rs556005703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841357 | TTCTTCTCAGCCTCC[A/T]GAGTAGCTGGGATTA | 5336 |
| rs556024432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848920 | GGTTTTCTGAGTTTG[G/T]TTTGATTGAGCTGAG | 5336 |
| rs556046080 | snp | C/T | 0.0205226 | 0.0991974 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854631 | TTCCCTGTGCCTTAG[C/T]GTCTTCCTGAAGAAG | 5336 |
| rs556063591 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952622 | TTTGCATAGCAAAAT[A/G]ATGATAATATCAGAT | 5336 |
| rs556069808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956555 | TTTGGTTAAAATAGG[C/G]CCTGGCTCTTCTGGG | 5336 |
| rs556075076 | snp | A/G | 9.93789e-05 | 0.00704837 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880993 | CGGGGCGGCTGTGCC[A/G]GACCTCGGTGCCTGG | 5336 |
| rs556091955 | snp | A/C | 0 | 0 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81779373 | GCGCGCGCGGGACCC[A/C]GGAGCCCAAACCCGG | 5336 |
| rs556112311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848763 | CTCAGTGGTGAAGAA[G/T]GGTGTACAATCCCTG | 5336 |
| rs556122598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829435 | GTTGACCAGGCTAGT[C/G]TCGAACTCCTAAGCT | 5336 |
| rs556147046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874727 | TCCATCGTGAGCTTG[C/G]TAGTTCCTCTTTGTG | 5336 |
| rs556174475 | snp | G/T | 1.66125e-05 | 0.00288201 | missense | PLCG2 | GRCh38.p7 | 16:81786002 | ACAATGTCCACCACG[G/T]TCAATGTAGATTCCC | 5336 |
| rs556175772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938662 | TGCAGAAGGTTGCTC[C/T]GGCTTTTCCAGTGAA | 5336 |
| rs556177179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856214 | GTGGGAAGATGAGAG[C/T]AGCAGTCTCTGCCAT | 5336 |
| rs556180632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914802 | GGTTGGTGAATGCTG[G/T]CTCAGTGAATCAATC | 5336 |
| rs556182070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800129 | AGGGGAGTTAATTAT[A/G]TATCATACTTTGGGT | 5336 |
| rs556187412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907175 | ACGTTATTAAAAAAA[A/G]GAGTTTCTGCATACC | 5336 |
| rs556207724 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941838 | ACCACATCTGGCTAA[G/T]TTTTGTATTTTTAGT | 5336 |
| rs556208603 | snp | C/T | 1.85713e-05 | 0.00304718 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870949 | CGGTAAGATGATTCT[C/T]GAGCAAGTGATCAAG | 5336 |
| rs556209006 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792089 | GATGGTGGCCACCAG[A/C]AGCCAAGCTCCCACA | 5336 |
| rs556211550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784479 | GAAGCACAGACAGCC[C/G]TGGCTGAACACCAGC | 5336 |
| rs556238725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799841 | CTCGTGATCCTCCCA[C/T]CTTGGCCTCCTAAAG | 5336 |
| rs556260023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878140 | GGCGCCCACCACCAC[A/G]CCTGGCTAATTTTTT | 5336 |
| rs556273068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784050 | CAGTGCATGCTTCTG[C/T]TGCTGCACTTGTAAC | 5336 |
| rs556280078 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81779283 | TGGCGCGGCGCCGCG[A/G]CCGAAGCAGAAGTAG | 5336 |
| rs556285894 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923095 | GTGATGACAGTCTTG[A/G]CTTAATCTAAAAGGC | 5336 |
| rs556286833 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955866 | TCTGCAAGATGTAAT[C/T]TATGATACCTTGGCT | 5336 |
| rs556317024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887896 | GGGTTTCTAGAATGT[C/G]TAGGACTGTGCAGCA | 5336 |
| rs556319497 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870160 | CAGAAGAGGAGAGAG[A/G]TGGGAGAAGCATTTA | 5336 |
| rs556344083 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809676 | GCTGTTTTCTCTGTT[-/C]CCTGCGGTGTGTGAG | 5336 |
| rs556350259 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960144 | GGAATCCACCATGAG[A/G]GAGTACTTTCTTCGG | 5336 |
| rs556350996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815022 | CTTGTTCCAGTGGCT[C/G]TTCCAGCCTGACAAA | 5336 |
| rs556351749 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891662 | GGCAGGGGTCCGATA[A/C/G/T]GCCGCTCCGGTGAGC | 5336 |
| rs556352641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871928 | AGCTGATTAAGAAGC[A/G]TGTGTCAGTTCTCTT | 5336 |
| rs556355878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915167 | TGGTCAGGCAGGGTG[A/G]TGGAGGGTGAGTAGC | 5336 |
| rs556366326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931308 | ACCCTACTGAATCTA[C/T]TGCATCCCTTGAGTA | 5336 |
| rs556366909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856807 | ATTGAGGATCTTGAG[A/G]TGGGAAATATCCTGG | 5336 |
| rs556380331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792430 | AGGCTGCAGTGAGCC[A/G]AGATCACTCCACTGC | 5336 |
| rs556385736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796990 | TCAGCCACTGATACT[A/G]TGGATGGGTTGTGGT | 5336 |
| rs556417666 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833628 | TCCACCTCCTAGGAT[C/G]AAGAAATGCTCCTAC | 5336 |
| rs556428054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935723 | GTTCTCCCTTCCCTG[C/T]ACAGGCACCCACATT | 5336 |
| rs556456481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853190 | ACAAAAACTAGCCGG[C/G]CATGGTGGCACATGC | 5336 |
| rs556475743 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944451 | GCATAGGTTATATGC[A/C]AATACTACGCCACTG | 5336 |
| rs556485640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867697 | CCCTTGCTTCCCTCC[C/G]TTTTCTTTTTTATTT | 5336 |
| rs556490695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804357 | AAACATTGGCTTTCT[G/T]TAGACAGTGTCCTAT | 5336 |
| rs556490740 | snp | A/C | 1.65756e-05 | 0.00287881 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81931625 | TGGTTTCAGAGCATC[A/C]GAGAGATCACCTGGA | 5336 |
| rs556495312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929082 | CTGGTTGCTCGGCTG[G/T]GGCCCAGGAAACCCA | 5336 |
| rs556505232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903370 | GGAGCTTTGGCCAAG[C/T]ACAACCAGAGGAGGG | 5336 |
| rs556508609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779888 | CGATACCGCGGGAGG[C/T]GCAGTCCTTCCCGGA | 5336 |
| rs556510686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920119 | GCCGGAATCAAGCCA[C/G]CCCAGGTGGGGGTAG | 5336 |
| rs556511748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805619 | TGAACAGATGCCTCA[A/C]ACCCCCTTCCCCCAC | 5336 |
| rs556535054 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799491 | GTGCAGTGGTGTGAC[C/T]ATAGGTCACTGTAGC | 5336 |
| rs556544578 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81798497 | GAAGGAGCGTCGACA[G/T]GGTGAAGGTGAAGTT | 5336 |
| rs556552120 | in-del | -/CC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803636 | TTTCTTTTCTTCTTC[-/CC]TCCCTCCCTCCCTCC | 5336 |
| rs556553865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807814 | TGAAGGCGGGGCTGG[C/T]ATGTGACATGGAGAA | 5336 |
| rs556561752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823004 | GAGACTGGTTTTGAC[C/T]TAGGAGCTGAAAGCT | 5336 |
| rs556581446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956974 | TGGAAAGCCCTCTGA[A/G]TTGCTTTCTTCAGAA | 5336 |
| rs556588287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804658 | TAGCACAGACTTTTC[A/G]TCATTTCAAGGTTTA | 5336 |
| rs556592992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834027 | GCTGCTGGAACGTGG[A/G]AATGGGGACAGGAGG | 5336 |
| rs556594494 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849363 | TAGAATTGTTAAAAT[C/G]TGGCTATTGCTGGAA | 5336 |
| rs556598849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859878 | ATGTGTTGGGTGATG[C/T]GATAACGTATATTCA | 5336 |
| rs556609711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829931 | GGGGGCTTATTCTAC[C/G]TCTCGGTGGCATCCC | 5336 |
| rs556614511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857362 | GGAGTCAGTGTGCTG[C/G]CAGGGTAAGATAATG | 5336 |
| rs556640277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956616 | GCTCCCTTTGGGCAT[C/G]CTTGTGAGATGCCAG | 5336 |
| rs556651262 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811695 | CCCTGCAAAGGACAT[C/G]AGCTCATCCTTTTTT | 5336 |
| rs556660980 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832092 | GGCCTCAGTCTTCTC[C/G]TTTGATAAATGGAGG | 5336 |
| rs556662120 | snp | A/G | 1.6669e-05 | 0.00288691 | missense | PLCG2 | GRCh38.p7 | 16:81908428 | CAGGATATACCCCCT[A/G]CAGAACTACATTTTG | 5336 |
| rs556670256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785849 | CTCATCCTGATTGAC[A/G]TGAGACAGGATTTTG | 5336 |
| rs556671924 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790540 | CAAGAAGAACTCCCA[C/G]CTCTGGCAATTTCCT | 5336 |
| rs556687540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811156 | AGTGTTGGGGTTGAA[C/G]AAGCCTGGGCTTGCC | 5336 |
| rs556707902 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81847940 | GGGATGACTGTATAT[C/G]TTATTAAAAGTCACA | 5336 |
| rs556710455 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962029 | CCTTCCTACCTCACC[A/G]CTCCATGTGCGTCCC | 5336 |
| rs556711694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948881 | ACTAAGGTACACACC[A/T]GGAATAGATGGCTGG | 5336 |
| rs556716686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809542 | GCCCCCAAATAAACT[C/T]CTTGTATGTACATCC | 5336 |
| rs556746860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896795 | TTTGTACAGGTGATC[A/G]TATTGATTCTTTGCC | 5336 |
| rs556746951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892198 | CAGAATCCAGGAGAG[C/T]GGTGTCAGGAGGGGA | 5336 |
| rs556746962 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835208 | TAATGACTCCTCTGT[C/T]GTAGGGTGGCTGGCA | 5336 |
| rs556746974 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849061 | AGGGGCCTGTGTGGG[A/T]GGTGCAAGGGCTGGG | 5336 |
| rs556748046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849725 | GCACTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 5336 |
| rs556761379 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861675 | GATGCCTCTTCTGAC[A/T]TTTCTTTCTCTGTGG | 5336 |
| rs556786567 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922567 | TTCCCATTTCACAGA[C/T]GGGGGAACTGAGGAT | 5336 |
| rs556786703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802522 | AACTGCTACCTTGAC[C/T]TACCACCTTCTCTTG | 5336 |
| rs556789143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900222 | GCACACGTGGAACAG[C/T]GTCCCTGTTGGTGAC | 5336 |
| rs556823855 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927872 | AGGTGTGGCAGTGGG[A/G]ATGTGGTTGTGTTCC | 5336 |
| rs556832038 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913725 | GGTGCTGGCTGCATG[A/G]CAGCTACTGTGGGGT | 5336 |
| rs556841233 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81860530 | TCCTGATGATTTATT[G/T]TGCCATTAGACTTTG | 5336 |
| rs556847975 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802270 | GGCGCCCGCCACCGC[A/G]CCCAGCTAATTTTTT | 5336 |
| rs556878786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929334 | CCCTAGGACTCAGGT[G/T]ACAGCAGCCCCAGGA | 5336 |
| rs556880786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925626 | GGTGCAGTGACTTGC[A/G]CCTGTAATCCCAGCA | 5336 |
| rs556881985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824737 | GTCCTTCCCCATGAT[G/T]TCACCTTTCATTGGA | 5336 |
| rs556883735 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836086 | AACCCCCAACATTAC[C/T]CGTTTATACTTTCTT | 5336 |
| rs556899688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901499 | CATTCTGCTCTAGCA[C/T]CTCTCAGGGCAGCAG | 5336 |
| rs556913246 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81820999 | TGACGTCAAATGATC[C/T]GCCCACCTCAGCCTC | 5336 |
| rs556937089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877034 | TGTTTCTGAAATGGG[C/G]CTTATTTTACTACCT | 5336 |
| rs556944757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830281 | GCTGTGATCATGCCA[C/T]TCACTCCAGCAGTGT | 5336 |
| rs556951657 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850636 | TCTTCCTGGCTCCCC[A/G]AAGACAGTCAGGAGA | 5336 |
| rs556979372 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882819 | ACTCTCTGGAGCTCA[A/G]GTAGGTGCCTTTTCC | 5336 |
| rs556981298 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958702 | AGAGAGACCAGAGCC[A/G]TGCTGCAGGGGCAGG | 5336 |
| rs556985296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831700 | GTTAGGGGGAACTTA[A/G]GCCAGAAGTGCCTGG | 5336 |
| rs556998705 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802828 | CACCCACCTCAGCCT[C/T]CCAAAGTGCAAAAGA | 5336 |
| rs557014725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809111 | CTGGTCTCTCTGAGC[A/C]TGGTGACTTGGACTT | 5336 |
| rs557021353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879600 | GAGTTCAGCAAGAGG[A/G]CCCTGGGTCATCTGG | 5336 |
| rs557023566 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840728 | CACCTCCTGCTGTGC[A/G/T]GCTCGATTCCTAACG | 5336 |
| rs557049203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937587 | GTTCCCCAGTCTGGG[A/T]GTTTGCTGTCTAGAA | 5336 |
| rs557054461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835345 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 5336 |
| rs557065100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882576 | GGCACACTCACATCC[C/G]TGTGTTCCCCACACC | 5336 |
| rs557067373 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835123 | TCTGTTATTGATTCA[C/G]TGTGTGACCTTGGAC | 5336 |
| rs557068848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870099 | CTTTGACCTGCCCCC[A/G]ATATTCCACATTAAT | 5336 |
| rs557069651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886550 | AATAGGAATGAAAAC[C/T]TGGAAGTAATCTAAA | 5336 |
| rs557070514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874050 | AAGATTCTGCCGATA[A/C]CAAAGGTTGACCCCT | 5336 |
| rs557080002 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866831 | TGCCGCTCTGGTAGC[A/G]CCTGTTCCCACTGCT | 5336 |
| rs557080530 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792200 | TAAAGACATACTCCA[A/G]CCTGGGCACAGTGGC | 5336 |
| rs557083326 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812804 | GGGTTTTTTATGGTT[G/T]TAGGTCTTATGTTTA | 5336 |
| rs557088528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922126 | CGCAAGTAGAGGCTG[C/T]TCTGTTTGCAGGTGG | 5336 |
| rs557108321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890438 | CAGATCTGTTTCACT[A/G]TCATAATTTTCTTGT | 5336 |
| rs557111457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880221 | ACTCCAGCCTGGGTA[A/T]CAGTGAGACCCCATC | 5336 |
| rs557115730 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955717 | CTGATCCCAAGAAAA[A/G]AAACTCTACCAAGAG | 5336 |
| rs557117869 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865046 | CAGGGTCATCACCCT[-/G]GGGGAAGGAAGGCAG | 5336 |
| rs557123113 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961414 | ATGTTTAATAATTTA[C/G]TGAAATTTGGGCTAT | 5336 |
| rs557142363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828875 | TGAATGCCGAGGTGG[A/G]TGGATCATGAGTTCA | 5336 |
| rs557170239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798753 | AAAATTAGGCAAGGC[A/G]TGGTGAGAGCATGTG | 5336 |
| rs557186736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824541 | GCTGGCACTTTTCGT[C/T]GGGATCATGTTTGGA | 5336 |
| rs557186864 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945467 | TCCTTTTAGGACAGA[C/G]AGGAGGATTGGGTGG | 5336 |
| rs557194331 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795218 | CAATCATGTTGGATC[A/G]TGATAGACGCTAGGA | 5336 |
| rs557197272 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880065 | GGCAACATAGTAAGA[C/T]CTGCATCTCTACAAA | 5336 |
| rs557201866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898280 | GTTTTGGCAGCAAAA[A/G]CCATCCTTATTGGTA | 5336 |
| rs557208908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946576 | TGCCTTCCTAGATAG[A/T]CTCATCCTTTCTGGA | 5336 |
| rs557214891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821122 | GTCTAGAACTCCTGA[C/T]GTCAAATGATCTGCC | 5336 |
| rs557234001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864030 | GGCATGGCCTCTGGC[A/G]TTGCAAATTTTTTAA | 5336 |
| rs557257157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828399 | CCTGCCACCACGCCC[G/T]GCTAATTTTTTTGTA | 5336 |
| rs557257829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902374 | AGGCTGGAAGTTCAA[A/G]GTCAGGGTGCTGGTA | 5336 |
| rs557265386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954676 | ACATTACTTCATTCA[C/T]TTTTGTGGCTGCATA | 5336 |
| rs557270597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876679 | GCACAGTGGTTAACA[A/G]TACAGCTGTTTCTCC | 5336 |
| rs557277094 | snp | C/G/T | 0.00254784 | 0.0356014 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938763 | GCTGCCTGTTCAGGA[C/G/T]CCCAGGGGGGTTCCA | 5336 |
| rs557304976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806611 | TCATAGGATAGCCTG[C/T]AGACATGTGATTCGT | 5336 |
| rs557319787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905684 | TATGTTGTGGGACAG[G/T]GTCTCACTCTGTCGC | 5336 |
| rs557320430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832070 | GCAGTGGGCTTTGTC[A/G]TCCTCCGGCCTCAGT | 5336 |
| rs557337692 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962760 | TAAAACACACACACA[C/T]ATACAATAATTTAGT | 5336 |
| rs557341790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782954 | AACCTGTGAGCAGCT[A/G]TTACAAAGCAATTGG | 5336 |
| rs557346020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832738 | ACACTTCTGTGAGTG[A/G]TATGATATCCAGTTG | 5336 |
| rs557349800 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822651 | AATCCCAGCTACTCA[A/G]AAGGCTGAGGCAGGA | 5336 |
| rs557384378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795550 | CACAATGGGACTCTG[G/T]GCTATCATCTCCAAA | 5336 |
| rs557388179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786640 | CTCCAAGCAGGGAGA[A/G]TGAGTTGTTGAACGT | 5336 |
| rs557396309 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904839 | GAGGAATAAAGCAGG[A/C]TTGGGGCTAGAGAGT | 5336 |
| rs557407543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821414 | AATGAATGAAATAAT[A/G]CAAATGTACATGTGT | 5336 |
| rs557411137 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803285 | ACCACGCCTGTCTAA[-/T]TTTTTTTTGTATTTT | 5336 |
| rs557415786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866556 | CACTGGGGCACCAGC[A/T]TGAGAGGACGTGGCC | 5336 |
| rs557424154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913857 | CCTCCTTGCCTGCAC[C/T]ACTATGCCTGAGCCA | 5336 |
| rs557437902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917791 | CAGTGGTGTGATCTC[A/C]GCTCACTGCAAGCTC | 5336 |
| rs557444282 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890060 | ATAGTGTGCTTCTGG[G/T]TGGGGCCACAGGACC | 5336 |
| rs557454832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844271 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCGCGC | 5336 |
| rs557457950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902113 | GTCAGCTGTCCCGTC[C/T]TTTTCTCTACTGTTC | 5336 |
| rs557461917 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853251 | CAGGATAATTGTTTG[A/T]ACCTGGGAGGCAGAC | 5336 |
| rs557467519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782119 | CTGACCTCATGATCC[A/G]CCCACCTCGGCCTCC | 5336 |
| rs557475507 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925850 | TGAGATCGTGCCATG[C/T]ACTCCAGCCTGGGGG | 5336 |
| rs557487486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913344 | TAACCGTGTTCTAGA[A/C]ACTGGACTGCCTTCA | 5336 |
| rs557493783 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843947 | TCCTTTTCCTTTTTC[C/T]TTTTCGTTTTTCTTT | 5336 |
| rs557501251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806941 | TGGAGGCCTCCATAG[C/T]ACTCAAGCTTTTCCT | 5336 |
| rs557508137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894393 | GTGATTGTGCCACTG[C/T]ACTCTAGCCTGGGCA | 5336 |
| rs557511272 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959056 | TACACCTCTGCATCT[G/T]AAGTTGTTAATACAT | 5336 |
| rs557511329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806036 | TTAACTCAGTATATC[C/G]AAAGCATTATTATTT | 5336 |
| rs557515685 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959693 | AAAGCAACTTTCAAG[A/G]AAGGCTAGGTGAGAA | 5336 |
| rs557520750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795638 | AGCAGAGGATGGCTC[A/C]GGAGGTTGGAGGTTT | 5336 |
| rs557533535 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950511 | ATCAGCAAAGACATA[A/C/T]TATCAAAATAATTTG | 5336 |
| rs557540771 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855461 | GAGGCAGCTGTCAAA[A/G]TTGAGCAATATAGGG | 5336 |
| rs557542012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833104 | AGGTGAGGGTGCTTT[C/T]CTGCTGGCACCCACC | 5336 |
| rs557559382 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803281 | CCACCACCACGCCTG[G/T]CTAATTTTTTTTGTA | 5336 |
| rs557560402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810530 | GTCACCCATTCACAC[A/G]TGCCCTGCTGAGGTC | 5336 |
| rs557561042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923057 | CCCTTGAGCTTCTGG[A/G]AGGCTTGCTGAGCAC | 5336 |
| rs557569433 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81921644 | TGCTATCTCATATTC[C/G]CACCCTGACTCTGTT | 5336 |
| rs557569752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882914 | CCCTCCCTTCCCACC[C/T]TCATCTCTTGCTACA | 5336 |
| rs557594864 | snp | C/T | 2.0405e-05 | 0.00319407 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905385 | TGGAGACAGCCTATG[C/T]ATATGTTTTCCCCTC | 5336 |
| rs557609464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863086 | TAACCGTTCTTAGAT[A/G]TGTACTTCTGTGGGA | 5336 |
| rs557629073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817498 | AGGGTGGTTTTAAAC[A/G]CCTTTTGTCAGCTGT | 5336 |
| rs557638060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887033 | TAGCTAAGTACCCAT[A/G]CCTTTTGATAAATGC | 5336 |
| rs557647194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798958 | TGCCACCAGCCTCCA[C/T]CAGTGGGAAAAGCCC | 5336 |
| rs557650479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910122 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 5336 |
| rs557663730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844289 | TGAGCCACCGCGCCC[A/G]GGCACCTTTTCATTT | 5336 |
| rs557705918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914242 | AGCGGTGAGACAGCT[C/G]TGACACAACCGGATC | 5336 |
| rs557710097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909729 | GAAAATTAGAATACT[A/G]ATAACACGCAAATAA | 5336 |
| rs557721323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874096 | ACATTGAGCCTGCCC[A/C]TGGTTGTACTTGATC | 5336 |
| rs557723804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898316 | AGGGATTTAAGAAAA[C/T]GATTGCAAGCAGCGT | 5336 |
| rs557724630 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836017 | TCCAAAGAAGGCCAC[A/G]TTCACACATACCAGG | 5336 |
| rs557767270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877085 | TGACTGAGACTGTCA[A/C]CGTCTTGCCCCAGCT | 5336 |
| rs557768885 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916077 | TCATTCTATTTTTAG[-/A]AAATACAAATGGGAA | 5336 |
| rs557793015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898645 | GTTTCATAGTAAATG[C/T]CATGCACAAGCCTCA | 5336 |
| rs557809388 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806360 | AGGTAGCTTTAATTT[C/T]CCACAGAGACTGAAA | 5336 |
| rs557819508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929340 | GACTCAGGTGACAGC[A/T]GCCCCAGGAACTTCC | 5336 |
| rs557833530 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854007 | GCTTTTGGGACTCAA[C/G]GGAAAAGGTCATCAA | 5336 |
| rs557837787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805642 | TCCCCCACCCCACTC[A/G]CAATGCTTTGCCATC | 5336 |
| rs557840317 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859234 | TTTAAACCTTCCAAG[C/G]GGGTGGGAGCATGAC | 5336 |
| rs557841897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962058 | CCTCCCGAAGCTGCG[C/T]GCTCCGTCGAAGAGG | 5336 |
| rs557854866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879664 | ATGTGATAGTGGATA[A/C]ATTTCCCTAAGTGCT | 5336 |
| rs557854938 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839844 | TCACTTGAGGCCAGG[C/G]ATTTGAGACCAGCCT | 5336 |
| rs557856755 | snp | C/G | 0.000798881 | 0.01997 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883557 | CTCTGGATGAGAAGA[C/G]CCTCATGTCGGGCCT | 5336 |
| rs557863834 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866923 | AAAGGTTCTTGCAAG[A/C]CCCTGGGGCAACTTC | 5336 |
| rs557870874 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806144 | TTTTATACCTATAAC[A/G]CATCTTGATTCAGAC | 5336 |
| rs557893443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887074 | TAGGGGGAAGGAAGG[A/G]GAATGCCTCCAGCCT | 5336 |
| rs557904954 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910166 | CGTGATCTCGGCTCA[C/G]TGCAACCTTCGTCTC | 5336 |
| rs557910633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877732 | GACACCATCACTCCT[C/T]GGCATGTAGGCGTCA | 5336 |
| rs557912674 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81779611 | TGGTGACGGCAGGGA[G/T]CCTGGCCCAGCCGCT | 5336 |
| rs557912712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951798 | ACAAATTAAATATGA[A/G]AAAAGCATAAACTAG | 5336 |
| rs557921608 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914272 | CGGGGCCTCACCTGA[G/T]GATGGTCAGGATGCC | 5336 |
| rs557932727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933646 | TGTTAAATGGAGATA[A/T]TTCTCCCTGTCAGGG | 5336 |
| rs557934845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894933 | CAACTACTGACTTAG[A/G]CTCCAGTGTTACCAA | 5336 |
| rs557935304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787201 | TTCGAAGTGACTATC[A/G]TTGTACTCTTTTTTT | 5336 |
| rs557936278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946635 | AATCCTATCAAAAAG[C/T]CTGATAGCCTCCAAT | 5336 |
| rs557948098 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780841 | AGACCAGCCTCACCA[A/G]CATGGTGAAACCCCA | 5336 |
| rs557958793 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778046 | ACAAAAAAAAAACAA[A/C]AAAAAAAACAAAAAA | 5336 |
| rs557992051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951205 | AGGCTGCTCTCAGAT[C/T]CTCCTGCCTTAGCCT | 5336 |
| rs557994158 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81829693 | AGTTTTTGTTTATTT[A/C]CATCGATATGTAGAG | 5336 |
| rs558004945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943021 | CTGGTCATGAGGGCA[C/G]AGCTCATGTCTCCGA | 5336 |
| rs558008177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821508 | CGGCTGACAGGCAGC[C/T]GTTGCCTCTTCTAAG | 5336 |
| rs558049273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802979 | AATGTTTCATAATTT[C/T]CCCCAAATCCTATAC | 5336 |
| rs558058883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899466 | CAAATCAAATCTCAA[A/G]GCACTCTGAGGTCAT | 5336 |
| rs558069266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953904 | TGAATTTTGAACTTG[C/T]GCCCGAATAACAAAT | 5336 |
| rs558077856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828800 | GGTGAAGTCGGGTAC[A/C]TAGAAGGTTTCAACA | 5336 |
| rs558087085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941135 | TTTTTGTTTTCAGAC[A/G]TTCCCTCAACTTCCA | 5336 |
| rs558109958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956088 | CAGACCCCGGTGACC[C/T]TTAACCTACTTTGTC | 5336 |
| rs558127286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877250 | GCGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 5336 |
| rs558133422 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824772 | GACTCCCTGCACATA[A/C/T]CCCCAAAGGTGTCCA | 5336 |
| rs558137154 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81791984 | CATCACTTGCACCAA[C/G]TCAGATCAGCAAGCC | 5336 |
| rs558138574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829249 | GAGTAGCTGGGATTA[C/G]ATGCACACACCAACG | 5336 |
| rs558138638 | snp | A/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959741 | CTGCAGGCACTCTGT[A/T]GCCAGGGCCCCATTA | 5336 |
| rs558162640 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811649 | CTTGTGTTAGTTTGC[A/T]GAGAATGATGGTTTC | 5336 |
| rs558162766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815863 | GTCAGGAGTTCGAGA[C/G]CAGCCCGGCCAACAT | 5336 |
| rs558178307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836842 | CTGCTTCAGCCTCCC[C/G]ACCTGTGGAAGGAAG | 5336 |
| rs558184545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783013 | ATGGCTGAGTTGATC[C/T]ACTGGGCTTCGAAGC | 5336 |
| rs558185097 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812931 | ATTTATTAAGTAGGG[A/G]ATCCTTTCCCCGTTG | 5336 |
| rs558192341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791899 | AAACATCTACCATGT[A/G]GTGGTCTCAGGCAGA | 5336 |
| rs558199866 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833148 | TCCTTCCCTGAGTCT[G/T]GTCTGTGAGAAGAGC | 5336 |
| rs558209120 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PLCG2 | GRCh38.p7 | 16:81779313 | GCGAGCGCCGGCGGC[A/G]GAGGGCGTGAGCGGC | 5336 |
| rs558211462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845795 | ACAAAAATGCCCACC[A/G]ACCCCCTCAGACTTT | 5336 |
| rs558224124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815689 | ATTTTTTCCAGTTCC[C/G]ATGCAGGTGGTGGCT | 5336 |
| rs558237279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844694 | TATGATCTGGATTGT[A/G]CATTTTGCATAAAAA | 5336 |
| rs558239731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836454 | GGTTAAGAGTGCAAG[C/G]TTTGGGCCGGGCAAG | 5336 |
| rs558245410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913908 | ACGGTCATTATCACT[A/T]TAGTTTACTGAGGAC | 5336 |
| rs558279155 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823104 | AGCAGGCGAGGCCTA[C/T]GTTGGCTGTGGTTTC | 5336 |
| rs558289158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840617 | TCCCTCACATGTGCA[C/G]TTCTCAATAAGGTTT | 5336 |
| rs558306033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879058 | GGTGGTACCTCTGCC[A/G]TTGTCCGAGCTCCCT | 5336 |
| rs558308988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803890 | TTTCACTATGTTGGC[A/C]AAGCTAGTCTTGAAC | 5336 |
| rs558312100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953751 | TGTTTCTATCTTTTA[C/T]GTTCTTTTCTGAATG | 5336 |
| rs558338285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827397 | TTTTGCCATGTTTCC[C/T]AGGCTGATCTCGAAC | 5336 |
| rs558373248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846487 | ACATTAGCACTCTGC[C/G]TAACACAGAGTAGGT | 5336 |
| rs558378785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855837 | GAGGAGGGAAATAGC[A/G]TGTCGGATGTAGGAA | 5336 |
| rs558385356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915907 | CAGTGAAGGCTAAAG[C/T]CCCCTGTGGTCCTTC | 5336 |
| rs558386617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902670 | TCTACCCTCATTCCC[A/G]TTCATGAGGACTCTA | 5336 |
| rs558399352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833492 | AGGTAAAAGGATACT[C/G]CTGCCTGTTTTTTTT | 5336 |
| rs558400073 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882262 | TTTTCTGGTGGCCTG[C/G]TGGCCAAGGCGGGAG | 5336 |
| rs558416087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859558 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTTTC | 5336 |
| rs558425620 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81845543 | TTCCAGAGTCTGTCC[A/G]CCTCATCAGTAGCGA | 5336 |
| rs558429808 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883848 | TTGCCTGTGGGCTCT[C/G]AGCCCAGCTATAGAC | 5336 |
| rs558436781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805356 | TATAAAAAATTAGCC[A/G]GGTGTGGTGTCGGGT | 5336 |
| rs558447420 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858498 | TCTTGTATGCAATGG[A/G]TGCCTAGTAGCGGTG | 5336 |
| rs558468258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937041 | AGGAATATGTCTATG[C/G]GACAGAATTCTCAGA | 5336 |
| rs558474868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893615 | TTTGGCGGCTCGGGC[A/G]GAGAAGTTCCCCCAC | 5336 |
| rs558476840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923677 | TCAGGTGCTGGCCAA[A/G]TCTGACCCCCTTTGT | 5336 |
| rs558478549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930502 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 5336 |
| rs558483701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831395 | GATAATAGCAGCAAA[C/T]ATTTAAACACAGGCT | 5336 |
| rs558504690 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835870 | CCTTGGCTGGTGGAT[A/G]TTGGCACTCCCATCT | 5336 |
| rs558512746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885226 | TCGGGGTTTCACAAT[G/T]TTGGTCAGCCTGGTC | 5336 |
| rs558520474 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916250 | CGAAATCGCTTAAAG[C/G]AATATATTTTTTTTT | 5336 |
| rs558526005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783475 | CTTTTGAGAGTGGCA[A/C]GTACTGGCAAATCAG | 5336 |
| rs558534733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865145 | CTGTGGAGCTGTCCT[A/G]AATTGAGACTAGAGG | 5336 |
| rs558537118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903836 | TGCAAAGTACTGAAG[G/T]CCCCTTTTAGAGCAC | 5336 |
| rs558545374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835260 | AAGCAGTTAATATAC[C/T]ACCTTACGTACAGCT | 5336 |
| rs558566218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893327 | GCCTTGATATCAAAA[G/T]AAGTGCCCATCTTTG | 5336 |
| rs558576966 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81793611 | GCTGCCCATGAGTGA[C/T]GGATTCTCAAACATA | 5336 |
| rs558577052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916358 | AAACAAAAAGTCTCT[C/G]TATAGTGCAAAAAAT | 5336 |
| rs558583815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785098 | AGTATGAGATCCTAG[G/T]AGGAGCCGGTGAAAG | 5336 |
| rs558591793 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81927905 | GTGCTTGGGCTGAGG[C/T]AGAGACTGGAAGCCC | 5336 |
| rs558595889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954131 | GGGCTCATGTGATCT[C/T]ACCCTCTCAGCCTCC | 5336 |
| rs558596283 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949442 | GACTTGTCCTCTTTG[A/G]TGCTGAAAACTAAAA | 5336 |
| rs558605468 | snp | A/C | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779109 | TCTTCTTTGGCACGC[A/C]GAGGCGGGGCTCCAG | 5336 |
| rs558606784 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913102 | GCAGCCCAGGCCTGT[A/G]ATGATATAGATCTGG | 5336 |
| rs558608411 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824195 | CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACC | 5336 |
| rs558610557 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915160 | AGGGATTGGTCAGGC[-/AG]AGGGTGGTGGAGGGT | 5336 |
| rs558613671 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898469 | AGTGAGCTGGGTCCA[C/T]GCTTCCCAGGAGTGA | 5336 |
| rs558635900 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820586 | GGAGATCTTGGGCAT[A/T]TCAGTTTTCCCCTCT | 5336 |
| rs558642976 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793908 | TTCCCAGTTTCAGTC[G/T]CAAGTCTTCTTCCTG | 5336 |
| rs558643054 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946654 | ATAGCCTCCAATCAA[C/G]TAGAATGACCATAAA | 5336 |
| rs558644528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838254 | ACCATGCCTGGCTAA[C/T]GTTTATATTTTTAGT | 5336 |
| rs558650948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842485 | TGCCTGGTTGACTGA[A/G]TAACTGAAAGTCGGA | 5336 |
| rs558690005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928681 | CCCCCATGGGCTGAC[C/G]TCAGCCCCGCCCTAC | 5336 |
| rs558696563 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873279 | AAAACTTTTAATACT[C/G]TTTAATCCCCTCTCC | 5336 |
| rs558699804 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892668 | AAAAAAAAAACTTTT[A/T]TTTTCAGTTCAGAGG | 5336 |
| rs558704244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901064 | AGAATGCGTGCAACT[A/G]CGCCTGTCATGTGGT | 5336 |
| rs558733258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876484 | TCCCTTTCTTAGTGC[C/G]CTGGCCCCTGCTTCT | 5336 |
| rs558738608 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853817 | TAACAGTCCATTACT[C/G]TGGACTGTTACCAGA | 5336 |
| rs558754428 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889862 | GGTTTCACTATGTTG[C/G]CCAGGCTGGTGTCGA | 5336 |
| rs558757805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901418 | ATTTCTTCCCCATGC[A/G]AGGGAGAATGTTCTG | 5336 |
| rs558759409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805219 | ACTCAACAATAAAAG[A/G]CCAGGCTCGGTAGCT | 5336 |
| rs558761498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957680 | ATAGTAGCCACCAAC[A/G]AGAAACTGTGCTGCC | 5336 |
| rs558764659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908897 | CCTACTCTTAGATGA[C/T]GTGGTCTCACTCACT | 5336 |
| rs558764942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801636 | CTTATTTTTTAAAAA[C/G]CTATCTCCCATTTTT | 5336 |
| rs558775662 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81797944 | CAAGCAATTATTCTG[C/T]CTCAGCCTCCTGAGT | 5336 |
| rs558794464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781745 | GCTCCATTTTAACAC[A/G]ATTGTCTTGTGGGAT | 5336 |
| rs558798120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932500 | TTCTAAGGTAGAACT[C/T]GACCCAAAGGGCTGA | 5336 |
| rs558836209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889390 | TGTATGATGTTGCCT[C/T]GACTGACTGGTTAGC | 5336 |
| rs558836633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853579 | GCATGCGTAGTTCAC[C/T]GTAGGGTTTGCGCCC | 5336 |
| rs558839100 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777619 | TATACACGCCAGTTG[C/G]GAGTGCTGAAAGAAA | 5336 |
| rs558840159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899865 | ACACACATAAAACAA[C/T]GTCAGATATTGATTC | 5336 |
| rs558848480 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782383 | AAGGGATTTCAAGGC[-/T]TTTTTTTTTTCTTTT | 5336 |
| rs558849285 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956106 | AACCTACTTTGTCTC[C/T]GTGATTTTGCTAGTT | 5336 |
| rs558858770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862150 | CTTTCCTGTCACCCA[C/T]GAGACGAATCGTGTT | 5336 |
| rs558883123 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958608 | AATTTCTAATTAATG[C/G]TGACAGCTTGTTTTG | 5336 |
| rs558896359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794265 | ATCCACTCTTGGACT[A/T]CTTTTCATGGAAAAA | 5336 |
| rs558906161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885012 | CCTGCCTCAGCCTCC[C/T]GAATAGCTGGGACTA | 5336 |
| rs558906641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945703 | GGAGGAAGATCAATA[C/T]TGCTATGAACTACTA | 5336 |
| rs558907513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875538 | GCGTAACAGACCCCC[A/G]TGTATCATCAGCTGA | 5336 |
| rs558927307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913276 | ATCTCCCCAGCCCCA[C/G]GGTTTCCCTGCATGT | 5336 |
| rs558938619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932202 | TTGGGAAGGTGTGAG[C/G]TTCTGGATAAGAATA | 5336 |
| rs558941216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846899 | AGATGTGTATGGTTT[C/T]CCCCCCACGCATCAA | 5336 |
| rs558945216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790598 | CTGGTTACTGTGGGG[A/T]CTGCAGGGGCAGGTG | 5336 |
| rs558950522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804930 | GCTCACATGTATCCA[C/T]GTGATCATGTGTATG | 5336 |
| rs558983262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816570 | TACTGCCTTGACCTC[C/T]TGGGCTCAAATGATC | 5336 |
| rs558991627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843445 | GCAATATATTACATC[A/G]TATTACACAGAGACA | 5336 |
| rs559003656 | in-del | -/TTTG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81884895 | TTTTGCAATTTTTTT[-/TTTG]TTTGAGATAAGGTCT | 5336 |
| rs559009971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794678 | GTAAATGACGTGATA[C/T]ATGTAAAATCCTTCA | 5336 |
| rs559012370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808285 | TGCCAAGGCCTGTTG[G/T]CTGTTTTGGAGGCAA | 5336 |
| rs559014966 | snp | G/T | 3.31835e-05 | 0.00407316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869165 | GCAGCTAAATCCTGT[G/T]CTGTTGAAAACCCTC | 5336 |
| rs559019550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946025 | CCATCAGGATAGGAC[C/G]TCTGGCTTCCACAAA | 5336 |
| rs559020998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851073 | ATGAGTCCTTTCTCT[A/G]CTTTCTCTCACCTTC | 5336 |
| rs559026869 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850832 | ATGCAGCCAAGGTGG[A/C]GGACTGGTCATTCTT | 5336 |
| rs559038807 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798310 | TGCATTTGTGTTTGC[G/T]TGGGGGACATGGGAC | 5336 |
| rs559054583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860470 | TGATAGCGAGAGGTA[A/G]CAATTTGTATAATAT | 5336 |
| rs559059031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853595 | GTAGGGTTTGCGCCC[C/T]TATGAGAATCTGATG | 5336 |
| rs559085282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925569 | AAGTTCTTCCCACCA[A/C]CACGGAGCACAGACT | 5336 |
| rs559100586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835855 | GTGACCCTGGGTGTC[C/G]CTTGGCTGGTGGATA | 5336 |
| rs559101525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801923 | TGACCACAAGTGATC[C/T]ACCCACCTCAGCCTC | 5336 |
| rs559101884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928143 | AGTCTTAAAAGCCAG[A/G]TCATAGAGCATGGGT | 5336 |
| rs559109359 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943412 | CACACTTTTATTAAA[C/T]AACCCCATCTCGTGA | 5336 |
| rs559153603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882104 | CATGTTTCATCTCTT[A/C]CACTATTTGAAATAG | 5336 |
| rs559156184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937956 | CGCCCTCCCTGGGGG[A/C]TGGGCCGATGCTGTC | 5336 |
| rs559160962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912888 | GAATGTGCGCTCCTG[C/G]GTGCCAGGCACAGTC | 5336 |
| rs559162111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809636 | CAGGAAACACATGGA[C/T]CAGACTTGGGCCACC | 5336 |
| rs559167585 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849451 | GGACAGATGCTCACC[A/G]TAGGCCAGTTCAAAG | 5336 |
| rs559171990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957106 | GAGTTCAAGACCAGC[A/G]TGCCCAACATGGAGA | 5336 |
| rs559206679 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866380 | AGCTCCACTGGGGCA[C/G]CAGCATGAGAGGACG | 5336 |
| rs559216947 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937623 | ATATTTTCTTTGAGT[G/T]AGATACCTATTTGAA | 5336 |
| rs559219743 | snp | G/T | | | missense | PLCG2 | GRCh38.p7 | 16:81928624 | AATACCTATAACGTC[G/T]GTACGTGCACACATC | 5336 |
| rs559229079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873579 | TTTAATAATAGTTTA[C/T]CTTGAAATTTCAAGA | 5336 |
| rs559242235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893370 | ACCCAGAGAGCGGCC[A/G]TGGGGCCTTGTTAAT | 5336 |
| rs559247201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823536 | TTTTCTTGTTTATTT[A/C]CTTTTAAGAGACAGG | 5336 |
| rs559254136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928453 | AAAATGCATTTTAAA[A/C]AGTTCCACAGGCAGT | 5336 |
| rs559284768 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81784471 | CCCGGCTGGAAGCAC[A/C]GACAGCCCTGGCTGA | 5336 |
| rs559292181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813593 | TAAAAACACAGGAGC[C/T]TAAAACAACAATTCT | 5336 |
| rs559292375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865876 | GGGGCACCAGCATGA[A/G]AGGACGCTGGCCTCT | 5336 |
| rs559299695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835460 | AATTCGCCGGGTGTG[G/T]TGACACTACTTGGGA | 5336 |
| rs559304575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872979 | ACTTTGGATGTATCT[A/G]AGTTAGAGAAATGGG | 5336 |
| rs559309631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853372 | AAAACCATTAGACCC[C/T]GAACTGGTACAGCAT | 5336 |
| rs559317910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885961 | AGTAAAATGAAGGTA[A/G]TAAGTTAATTTTATT | 5336 |
| rs559323869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797981 | GATTACAGGTACCCT[A/C]CACCTCACCTGGCTA | 5336 |
| rs559329422 | in-del | -/AA | 0.00347825 | 0.0415575 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858441 | GGCTACAGGGGGGAA[-/AA]AAAAAAAAAGGGACA | 5336 |
| rs559354109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885617 | TATGTTTCTCTCACA[C/G]ATAGAACTTTTTTTT | 5336 |
| rs559354443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777844 | AACATAGTGAAACCG[C/T]GTCTCTAGTAAAAAT | 5336 |
| rs559360057 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961622 | AAAGGAAAAGTGGGG[C/T]ATTCCTTGCTACTAA | 5336 |
| rs559365076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850048 | CTTTAAAAAGTCAAA[A/G]GCACAAGAGAAAACA | 5336 |
| rs559368257 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797056 | CCACGTGTCATGTTA[G/T]TTTCTAGCTGCGTTG | 5336 |
| rs559405939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881667 | TATGTATATTCGAGA[A/C]GGAGCCTCCCTTTGT | 5336 |
| rs559417434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827484 | ATGAGTCACTGTACC[C/T]GGCCTGCATTTATTT | 5336 |
| rs559434144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900434 | TTCTGAGTCCCAAGA[C/T]TTGTGCCTTCACACC | 5336 |
| rs559434357 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81944291 | AACCAACCAAGCTTG[G/T]GTTGAAAATATTTTT | 5336 |
| rs559446245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903631 | GGGATGCTTCCAGCA[C/T]GGTGAAGGCAGGATA | 5336 |
| rs559460286 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81800062 | TTTCATTGCACTCAT[C/T]TGTAAAATAGGATAA | 5336 |
| rs559472126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851227 | GGCAAAAATAGTACA[C/G]TTTCTGTGAACCATT | 5336 |
| rs559477047 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961057 | ATCAACAGGGCACAA[A/G]TCTTTTTGCAAATGG | 5336 |
| rs559483893 | in-del | -/CTGA | 0.001228 | 0.0247486 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959969 | ACCATATCAAAGAAC[-/CTGA]CTGACATATGGCGGC | 5336 |
| rs559500618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901876 | ATCTTAATCATGTTT[C/T]AATATAATTGAGTTT | 5336 |
| rs559507530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834534 | GCTTTGGGAGAGACC[A/G]CTGAGATGATGGACA | 5336 |
| rs559544781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893061 | AGACAGAATTTCACT[A/T]TGTTGGCCAGGCTGG | 5336 |
| rs559564889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853561 | ACACAACCTGGATCC[A/C]TCGCATGCGTAGTTC | 5336 |
| rs559564934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901552 | CCCCCGAAGAATCCA[C/T]GGTTAGAATCAGAGG | 5336 |
| rs559599919 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914830 | ATCAGCAAGGATGGC[C/T]GCTCCCCACCTCACC | 5336 |
| rs559602870 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781997 | CTGCCTCAGCCTCAC[A/G]AGTAGCTGGGATTAC | 5336 |
| rs559611479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953358 | TGTGCGAGATGTTAA[C/T]ACTGTGGAGTCTAGG | 5336 |
| rs559611907 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81875620 | ACTTTGCAGCAGACA[G/T]CAAGCAGCGTATCAG | 5336 |
| rs559614742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843089 | GTGGCTGGGTTATCT[C/T]ACTTTCTTCAAGCAG | 5336 |
| rs559617757 | in-del | -/GTCA | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941034 | AAGAGAAAGATGACT[-/GTCA]GTCATTTTAGTTACT | 5336 |
| rs559619566 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961895 | AATTCACTTAAGAGT[A/G]TCTGAGCATAAAATG | 5336 |
| rs559634317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835877 | TGGTGGATATTGGCA[C/T]TCCCATCTCTCCCTC | 5336 |
| rs559640767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904393 | ACCAGGTTACATGAC[C/G]CTCAACTTACAGACG | 5336 |
| rs559656318 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899406 | TAGAAGGATACAGGT[A/G]ATCCTTATTGGTGGA | 5336 |
| rs559663957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802367 | TCCACCCGCCTCGGC[A/C]TCCCAAAGTGCTGGG | 5336 |
| rs559665761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857453 | AATGCTGTAGACTGG[G/T]GGTTTAAACATCAGG | 5336 |
| rs559667709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883858 | GCTCTGAGCCCAGCT[A/G]TAGACTCAAGGGGGG | 5336 |
| rs559670168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850543 | AATTGACAAGAGGTC[C/T]AAAGAGTTTTCCCAG | 5336 |
| rs559670285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920968 | ACGCAGTGCCTGGCA[C/T]GCAGCAGGCCAGGAC | 5336 |
| rs559679366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828102 | TCTCAAAAAAAAAAA[A/G]AAAAAAAAAAGTTGA | 5336 |
| rs559680845 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963075 | ACAGGAAGCCATGTT[A/G]TATCTCATACCTCTG | 5336 |
| rs559702591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937256 | TTTTTGCCGTTTGCA[C/T]AACTGAGAGGTGAAA | 5336 |
| rs559703934 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780006 | GTTGTGTTTTGGAAT[C/G]CCAAAGAGGGCATTA | 5336 |
| rs559708349 | in-del | -/ATATA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801353 | TCATCCATGATTAAC[-/ATATA]ATATGTTTTGCAGGT | 5336 |
| rs559744917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809263 | GGCTTCTGCTAGCCT[A/G]TGGTGCAGGATAGGC | 5336 |
| rs559751905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779572 | ACCCTCGGGGACCCC[A/G]GCCCGCCGTGCCCGG | 5336 |
| rs559752221 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861841 | TGGATACCACCCTCT[G/T]GCTCAGGAGGCATTC | 5336 |
| rs559753160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785729 | CGGTTGGGTCCTTGA[A/G]GTCAGGGGCTCTTCT | 5336 |
| rs559760160 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848784 | ACAATCCCTGCGTGT[A/T]TGGAGCTTACAGTCT | 5336 |
| rs559767016 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941503 | TTACCATTGAGGAAA[C/T]GAATTCCTTAGCAAG | 5336 |
| rs559770025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879524 | CTCTCTGATGCTTCT[C/T]AGAGGCCTGCGATTC | 5336 |
| rs559774707 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932688 | TCACTCAACTCTTCT[C/G]CAGGGAAGTGTCCTC | 5336 |
| rs559775444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812205 | CAGGCACCTGCCACC[A/G]CGCCTGGCTAATTTT | 5336 |
| rs559781995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928972 | TGGCTGAAATGCAGC[A/G]TGGAGTTGGGAGTCT | 5336 |
| rs559802057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882655 | CCTCTTTCTTTCCTC[C/T]CCTCCCTTCTCTTTT | 5336 |
| rs559814609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779927 | GAGAGCTTGCAGGAC[A/C]CTCGCGATGCCCGCT | 5336 |
| rs559819025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912986 | ATGACCATGATCCGT[A/G]TTTCTCAGAGGAGGA | 5336 |
| rs559841784 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790177 | CATAGTGTGTGACAG[A/G]CACTCAGTTGTTGGG | 5336 |
| rs559871246 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913567 | CAGAGGCCTGGGGGC[C/T]AAATCTCCAGCCAGA | 5336 |
| rs559890227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852495 | GTTGAGCTTGTTGAG[C/T]TTGTGTCTCTGTGCC | 5336 |
| rs559891067 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81934889 | AAACCATCAGATCTC[A/G]CGAGACTTATTCAGT | 5336 |
| rs559893051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939077 | GAGGGGATACATACA[A/G]AGGGCCACTTTCTGA | 5336 |
| rs559901739 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789853 | ACCTTTGCCCCCCCT[C/G]CATTGCCTCCCCTCT | 5336 |
| rs559903657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794373 | AATGAATTATTTTCT[C/T]GCTGGCATCTCCTAA | 5336 |
| rs559905143 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920184 | TCATGCAGGGGCTCA[C/T]AGGCCATTGTAAGGC | 5336 |
| rs559915711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865343 | GGTTTTGGTCGGGCT[C/G]TGCAGCACGACACAC | 5336 |
| rs559921689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910402 | AGCCTCCTGTGTCTG[C/T]TCTAGGAGCAGAGGG | 5336 |
| rs559930951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802203 | CTGCAAGCTCCGCCT[C/T]CCGGGTTCACACCAT | 5336 |
| rs559932296 | snp | C/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962056 | TCCCTCCCGAAGCTG[C/T]GCGCTCCGTCGAAGA | 5336 |
| rs559944047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787459 | TCTCCAATTCCTGTG[C/G]TCAAGTGATCCTCCC | 5336 |
| rs559959916 | snp | A/C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890974 | TTGAGACCAGCCTGG[A/C/G]CGACATGGTAAAATT | 5336 |
| rs559961624 | in-del | -/AC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81830679 | TGTATATATATATAT[-/AC]ACACACATATATTTT | 5336 |
| rs559973672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854020 | AAGGGAAAAGGTCAT[A/C]AAGGTCAAGGTCAAC | 5336 |
| rs559978897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813938 | GAAATAGATTCTACC[C/T]GTTGATGGGAAGAAG | 5336 |
| rs559986554 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829201 | GCAACCTCTGTCTTC[C/G/T]GGGTTCAAGCGATTC | 5336 |
| rs559993229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944985 | GCCAGAAAAACATAA[C/G]CCTCCCTTTGTGGGA | 5336 |
| rs559996390 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842249 | GCAGAACTCAGCCAG[A/G]ATGCATGTGCTCAGA | 5336 |
| rs560004077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929240 | GGGTGTGGTGCAGCT[C/T]CCATGTGAAGGGACT | 5336 |
| rs560007160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879223 | TGGGTGTGGGGCTTT[C/G]GGCTTGGAAGTGTTC | 5336 |
| rs560024350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805765 | GAGTAGTGTTTTGTT[G/T]TGTTTTTTTTTTTTT | 5336 |
| rs560033924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837436 | GCTGCATGAACATCT[A/G]TTTCTAGCTGGGCGG | 5336 |
| rs560038909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817715 | GGTCTAAAACTCCCA[A/G]ACTCAAGCGACCCCC | 5336 |
| rs560042258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783711 | GCCCAATAAATGGCT[C/G]CTTAACAAGGATGAA | 5336 |
| rs560072753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951703 | TAGCAAATATCCAGC[A/T]GTTTACTAGAAGAGC | 5336 |
| rs560084119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787891 | CATCCACTTTGTTGC[A/G]TGGATCAGAAATTTT | 5336 |
| rs560088463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919943 | TGGATAAGAGGATAC[A/C]GAGTGATGGGGAAGG | 5336 |
| rs560089080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805509 | ATCTCAGAAAAAAAA[A/C]AAAAAAAAACAAAAC | 5336 |
| rs560114705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803721 | CAGTCTCACTGTGTC[A/G]GTCAGGCCGGAGGGC | 5336 |
| rs560118013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933228 | GTCCTGTTATTACAT[C/T]TGAGGGGTAAAAAAA | 5336 |
| rs560118435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814367 | GGAGTGGAGGATCTG[C/T]GAGGTGGGGTGTAGC | 5336 |
| rs560144689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829315 | GATTTCACCCTGTTG[A/G]TCAGGCTGGCCTTGA | 5336 |
| rs560147020 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878312 | TTTAAGAAGCCAGGC[A/C]CTGGATTCGGGTCCA | 5336 |
| rs560152707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796808 | GAACCAGCCTCGCCA[A/G]CACTTTGATTTTGGA | 5336 |
| rs560162320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849377 | TCTGGCTATTGCTGG[A/G]AGACAATGTTACCTT | 5336 |
| rs560178153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818014 | AGACCTGGTTGTCAT[C/G]TACTCTCTGTTCCTT | 5336 |
| rs560181132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935000 | ATGGGAGCTACAATT[C/G]AAGGTGAGATTTGGG | 5336 |
| rs560203964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833341 | ATCTGTCCACACCCC[C/T]AGGGTCCTTTTTCCT | 5336 |
| rs560221720 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859346 | CTCCTCCTGGAGGGA[A/G]CCTCTATTCCGCAGA | 5336 |
| rs560286327 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81815618 | GCTCAAAAGCCACTC[A/G]GAACACAAGTCCCTC | 5336 |
| rs560288980 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818533 | TACTCATCGGCTGCA[C/T]GGAAATGGAGCTCCG | 5336 |
| rs560301961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936431 | TGGCGGTTGCAGTCA[C/T]TCCAGGCCGAGTCAC | 5336 |
| rs560302412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855984 | GCTGAGCCCTGACCC[C/G]CTGTTCTTAATTTGG | 5336 |
| rs560323248 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816302 | CTTGAACCTGGGAGA[C/T]GGAAGTTACAGTGAG | 5336 |
| rs560341469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931347 | TGATGTGTACTTACC[C/T]CGATGGAAAGTAGAC | 5336 |
| rs560342701 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960182 | CTCCTGTCCTTGACA[C/G]AGTAACACGTTAATC | 5336 |
| rs560361910 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804109 | CTGTAACTGTTTAAT[C/G]ACTTAAGGAATTGCC | 5336 |
| rs560372435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877926 | ATCACATGGACCCCT[C/T]TTCTCTGTGTGCTTC | 5336 |
| rs560402637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915955 | TCCTGGTAGAAAGCA[C/T]AGTTTTCTAGCTGGT | 5336 |
| rs560402811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931012 | TCAACCAAAAAGATA[C/T]TCAGTGTTTCTTTTG | 5336 |
| rs560406235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884017 | GGATGTTCCTAAATA[C/T]CCTACATTGCACAGG | 5336 |
| rs560413726 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81939071 | CTTGAGGAGGGGATA[C/T]ATACAAAGGGCCACT | 5336 |
| rs560414777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920140 | GTGGGGGTAGAGCTA[A/C]ATAAGGATGAGGGTT | 5336 |
| rs560417020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807496 | ATCATTGTCATCACT[C/G]TCACTAACGCCACCA | 5336 |
| rs560428536 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935190 | GGGCTGTGCTCCCTC[C/T]GGAGGGGAAAGCCAT | 5336 |
| rs560444069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811721 | TTTTTATGGTTGCAT[A/G]GTATTCCATGGTGTA | 5336 |
| rs560462880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807231 | CGGTGTCCTCCTCCT[A/G]CATCAGGAGAGGGAG | 5336 |
| rs560471884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935411 | ATTAGGGCCTGGACA[G/T]CTTTGGGGGCCATTT | 5336 |
| rs560473714 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956404 | GACCAAAGGAAAACC[A/C/G]GGTTAGATTAAGAAA | 5336 |
| rs560480086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891821 | GGCCCTAAAAAGCTA[C/G]TAAAAACAAAAGTAA | 5336 |
| rs560510238 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948067 | AACGGAGAGTCAAGT[C/T]GTTGGCAGTTCTTTA | 5336 |
| rs560513343 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808751 | ACCTGCCTCTGCCTC[C/T]CAAAGTGCTGGGATT | 5336 |
| rs560553539 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795464 | AACAAGTTATTTCTT[C/T]CTGTAAGTTTATCTC | 5336 |
| rs560554103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871734 | TATGTTTTGATCTGA[C/G]AGTGGCATCCTGGGG | 5336 |
| rs560556709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842283 | GCCTTTCTTCCCCTT[C/G]CTGGGGAGGAGCCCC | 5336 |
| rs560578612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884040 | TGCACAGGGCAGCCC[C/T]CCCTACCCCCCAGCG | 5336 |
| rs560579807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896046 | AATGCGGGAAGGCCT[A/G]GGCCCCATCTTGGCC | 5336 |
| rs560584227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952077 | CCCATTTGTGATACT[A/G]ACAAAAACCATAACA | 5336 |
| rs560612866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874861 | TGAGGGGATATACCT[C/G]TAACTAGGCTGTAAT | 5336 |
| rs560615398 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821175 | GGGATTACAGGCGTG[C/T]GTGAGCCGCCGTGCC | 5336 |
| rs560618481 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874736 | AGCTTGCTAGTTCCT[C/G]TTTGTGTCTAACCAC | 5336 |
| rs560630107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814836 | CCTTAGTTTCTTTGT[C/G]TCTGCAGTGGGGATT | 5336 |
| rs560646080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834263 | TTCAGTAAGGGGGAC[A/C]TGGTTTGTTCTCTGT | 5336 |
| rs560648069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838351 | CTTGGCCTCCCAAAG[A/T]GCTGGGATTACAGGC | 5336 |
| rs560651211 | snp | C/T | 4.96882e-05 | 0.00498414 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81956799 | CCAGAACTTGCGCAA[C/T]GCCAACCGGGATGCC | 5336 |
| rs560676129 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81911946 | GGGACTACAGGCGCC[C/T]GCCACCATGCCTGGC | 5336 |
| rs560691816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818422 | TGTTCCATTCATTGT[A/T]CCTGTGTCATGCATG | 5336 |
| rs560698868 | in-del | -/A | 0.449435 | 0.15075 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916299 | TTTTTTAAAAAAAGA[-/A]AAAAAACAACGTTTT | 5336 |
| rs560703035 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888469 | TGAGCTCAGGCAGTC[C/T]ACCCGCCTCGGCCTA | 5336 |
| rs560711809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880754 | TTAAGTTTCTGTTAT[A/G]TTTGAATATTTACAA | 5336 |
| rs560715998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896111 | GGCACCCCCTGCAGG[C/T]CGAGAGTGCAAGTTG | 5336 |
| rs560737001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884942 | GCCCAGGCTGGAGAG[C/T]AGTGGCATGGTAACA | 5336 |
| rs560741599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892939 | AACCTCCGCTTTCCC[A/G]GTTCAACAGATTCTC | 5336 |
| rs560750830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811376 | TTGCACGTCGGGGTT[A/C]AGGACTCAAAAGGGA | 5336 |
| rs560771131 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811171 | CAAGCCTGGGCTTGC[C/T]TCCTGAGTCTCCCAT | 5336 |
| rs560789379 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858662 | TTCTTAAAGGATTTA[A/G]TAAGAGATTCAGTGG | 5336 |
| rs560790573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892279 | TCGGGGAGACCCTGA[C/T]GACTTTTAACCAGAA | 5336 |
| rs560793742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788889 | CTGGGGTGGCCACCC[G/T]CCCTTCCCCCACAAG | 5336 |
| rs560797209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957032 | GGCCAGGCATGGTGG[C/T]TCATGCCTGTAATCC | 5336 |
| rs560799994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810822 | GGTCTTTAATTTCAT[C/T]GACCTTATTGTTTAG | 5336 |
| rs560808244 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795226 | TTGGATCGTGATAGA[C/T]GCTAGGAAGGAAAGG | 5336 |
| rs560816154 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815280 | TGGTGGGCCCAGGCT[A/C]GAGCATGGGTCTCCC | 5336 |
| rs560824171 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931108 | CATTTTAATGTTTGT[G/T]TTTTTTTCCTGCATC | 5336 |
| rs560829049 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81848501 | CCTTTGTACATGTGC[A/G]TTTGCATTTCTCTCC | 5336 |
| rs560830207 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856012 | TGGTAAGGAGACCAG[A/G]AGAACCCGGGTCTTG | 5336 |
| rs560860307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814491 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 5336 |
| rs560863617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834195 | GGCTTTCTTCCCAAG[A/G]TTGGTGGGAGGATTA | 5336 |
| rs560868766 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859699 | GCCACCATGCCCGGC[G/T]AATTTTTTTTGTATT | 5336 |
| rs560869402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822311 | TGATTGATGGCCCCC[A/G]GAGATGTCCATGTCC | 5336 |
| rs560871407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868107 | ATCCAGGCTCTGCTG[C/T]CTGCCATCCAGCTCT | 5336 |
| rs560876796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924118 | GAATTGAAGACAATA[C/T]GTTTTTCGTGCAAAG | 5336 |
| rs560893170 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849277 | ATAGACAAGAGATAA[C/T]GGTGGCTTGGATTGT | 5336 |
| rs560899483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911144 | TCTTGCGAAGGGTCA[A/G]CAAATTCTGGGAATA | 5336 |
| rs560904571 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794714 | ATCTGGCACAGAGGA[C/T]GTGCTTAAGTATTTT | 5336 |
| rs560909908 | in-del | -/TG | 0.00159617 | 0.0282053 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81962880 | AGCAAAAACTCACTC[-/TG]TGTTGAAACTCAAGT | 5336 |
| rs560924029 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788366 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGATTCAT | 5336 |
| rs560965047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910857 | GCATCTCAAAATTGC[C/T]GAGGTGGCCAGTTTC | 5336 |
| rs560972964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914955 | CCCTGGTCTCTACCC[A/C]CTGCATGTCTGTCTG | 5336 |
| rs560973308 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836072 | GGGGATGCAGTTCAA[-/C]CCCCCAACATTACCC | 5336 |
| rs560974356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846253 | GACTGGCCTCCCTTC[A/C]TTCAGGAGGACCTAC | 5336 |
| rs560992846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780460 | TTGACTACAGTTCTG[C/T]GGGGAAGTTTTACAG | 5336 |
| rs561020330 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928028 | TGCCTGGTTCTGCCA[C/T]CTCTCCTAAGCCCAG | 5336 |
| rs561022449 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81956234 | GCTTGTTACCTTGCC[-/T]TTTAAGGCCCTTAAA | 5336 |
| rs561023174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807879 | CATACTTTTCAACAG[A/C]CAGATCTCTCAAGAA | 5336 |
| rs561026960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863892 | AAGGCAGGTGGGTGA[A/G]TCCATTTATCTCATT | 5336 |
| rs561027377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878012 | TTTGAGAGGGAGTCT[C/T]GCTCTGTCACCCAGG | 5336 |
| rs561039109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841483 | TGACCTCAAGTGATC[C/T]GCCCACTTCGGCCTC | 5336 |
| rs561044693 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81835480 | ACTACTTGGGAGGCT[G/T]AGGTATGAGAATCGC | 5336 |
| rs561050650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902942 | TCACTATCACAAGAA[C/T]AGCACGTGAAAGGCC | 5336 |
| rs561051161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875205 | CTGACCTCAGGTGAT[C/G]CTCCCGCCTTGGCCT | 5336 |
| rs561058548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784704 | GGCCTGAGATACATT[A/G]TCTTGTTTAAGCCTT | 5336 |
| rs561081991 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81823804 | CAAAGTGCTGGGATT[C/G]CAGGCATGAACCACT | 5336 |
| rs561086816 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942249 | ATGTCAGAGTTGATG[A/G]TAAAACCTCGTTACC | 5336 |
| rs561101112 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804471 | TATGTTAGCTTGCAG[C/T]ACATGGGCATGGACA | 5336 |
| rs561108149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793515 | GGATGCGTCCATCTC[A/C]ACTGTGTAGGCTTTT | 5336 |
| rs561110482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857108 | CTAAGTTTGTGGTCA[C/T]TTGTTATAGCAGCAG | 5336 |
| rs561124290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911076 | AAGGAAACAATGATT[A/G]TAAGAGTCTCCCGCT | 5336 |
| rs561147257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860904 | ATTGCTTGAACCCGG[G/T]AGGTGGAGGTTGCAG | 5336 |
| rs561162635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804147 | TTTGCCAAAGCAGTT[C/G]CACCATTTACTTTCC | 5336 |
| rs561163399 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877679 | GCAGTCCTACAAGTG[G/T]TCCTCGGTGTGTAGA | 5336 |
| rs561163863 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958890 | AGTTAGGTTGATGGC[A/G]AAATGTCTCTGGGTT | 5336 |
| rs561174653 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852911 | GGCATTGATTCTTCT[G/T]CCATGGCCTCTCCAT | 5336 |
| rs561175322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797517 | CAGACTAAGAGTGCT[A/G]GGAGGCCAGGGACCC | 5336 |
| rs561175665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868181 | TTCTGAGCCCTGGGG[A/G]TCAACCATGTGTACT | 5336 |
| rs561192103 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823436 | AGGTGAAGATTGAGT[C/G]GGGGTAGGGGCTGCA | 5336 |
| rs561196328 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81885212 | TATTTTTAATAGAGT[C/T]GGGGTTTCACAATGT | 5336 |
| rs561206010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891844 | AAAAGTAACTTAGTT[A/T]ATGTAACTTAGTAAC | 5336 |
| rs561206473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789794 | CCCCCTCCTCTCCCT[C/T]CTCTTCTCCCTCCCA | 5336 |
| rs561217644 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792386 | ACTTGGGAGGCTGAG[A/G]CACAGAATTGCTTGA | 5336 |
| rs561223204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860544 | TGTGCCATTAGACTT[G/T]GATCTTTGTTCATCT | 5336 |
| rs561238808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849898 | TCACTAGACTTTCAC[G/T]GGCAGTCAACTGGGT | 5336 |
| rs561245626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881119 | CTGTGGCGTGGATAG[A/T]GATGAGCAGTAGCAA | 5336 |
| rs561254268 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911632 | TTAATTAATTTTGAG[A/C]CCGGGTCTCGCTCTG | 5336 |
| rs561255877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906948 | GAGGCTGAGGCAGGA[A/G]AATTACTTGAACCCG | 5336 |
| rs561261053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940287 | GGGATGTTTACAAGC[A/G]AAACTGGATTGTTAG | 5336 |
| rs561271324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815333 | CCTCAGCAGGTTGGC[A/C]GCCACACAACACAGT | 5336 |
| rs561275979 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952283 | TATATATATTCACAC[A/G]TAGATGAATAAATGT | 5336 |
| rs561276623 | snp | A/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960130 | CTGGTGCTACAACCG[A/G]AATCCACCATGAGAG | 5336 |
| rs561292453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888491 | CTCGGCCTACCAAAG[G/T]GGGTCTGAGCACTTT | 5336 |
| rs561292507 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836532 | GATCACCTGAGGTGA[A/G]GAGTTTGAGACCAGC | 5336 |
| rs561321407 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917910 | GTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 5336 |
| rs561323669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834975 | TCTGGAGAACAGACC[C/T]TGTGGGCAGGGGAAA | 5336 |
| rs561328284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872059 | ACAGGCCAGGTGCAG[C/T]GGTTGACGCCTGTAA | 5336 |
| rs561331014 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81928086 | GGATGGTTCAAGGGT[A/G]CAATGGGAGGCAGAG | 5336 |
| rs561331411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791019 | AAAATGTCACTGGGT[A/G]AAATAGGGTTTTGCT | 5336 |
| rs561351469 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945574 | CTTAAACATTACTGA[A/G]TGGGGGTGGGGGAGA | 5336 |
| rs561384446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839012 | CATTTCCCTTTATGA[C/T]TCACAGAACCAAGCC | 5336 |
| rs561392447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795002 | GTCTTGTTTTCAAGA[A/G]TTGTCTTCTATCCTG | 5336 |
| rs561394319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847542 | CAAAAAGATACTTAT[C/T]ACTGCAGATTCCAAG | 5336 |
| rs561395041 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811945 | TCGAGGAATTGCAAC[A/G]CTGTCTTCCACAATG | 5336 |
| rs561413660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865259 | AGGGGATGGCAGGTT[C/G]CAGAGAGGGGTGAAG | 5336 |
| rs561417218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875484 | TTTTGAATCCTTTGT[A/G]TTAAAGAAAATGTAA | 5336 |
| rs561417273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871788 | CATCGGGGCCTGAGA[A/G]TATATTATCGGATTG | 5336 |
| rs561431240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851474 | ACAGGATGTAGATGA[C/T]GTGCTGTTTTTTTAC | 5336 |
| rs561454193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936528 | CAGAGTAATGGTTAG[C/T]ATGAGGTCCAGCAGC | 5336 |
| rs561459837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847347 | TGGGTTTTTATGAGA[A/G]CCTAATTACAAAGGC | 5336 |
| rs561460914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823147 | CCTCTTGGATGATGG[C/T]GCCTTATGGTCATTT | 5336 |
| rs561465541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830747 | TGCCAAGGGCTGCAG[A/C]TGACTCCAGAGGACC | 5336 |
| rs561478368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924563 | GATTTGAACCGCCAG[G/T]CCTTTTGACTCCAGA | 5336 |
| rs561479776 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81948960 | CATAACTCATAGGAT[C/G]TTTCAAAGACATCCA | 5336 |
| rs561507575 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961139 | GAGGAACAGCCTGTA[A/G]ATTTCTGAGTCTCTT | 5336 |
| rs561514279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858876 | GGGGATTAAATGACT[A/G]TCATCAGAAGGAATT | 5336 |
| rs561548737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862852 | GCTCCAGCCTGGGCA[A/G]CAGAGTGAGATCCCA | 5336 |
| rs561552993 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936839 | TGTTATTTAAGACCT[A/C]TTTCGAGGGATCTAT | 5336 |
| rs561562623 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862409 | TATGCTCTTGGCTGA[C/G]GGTTGAGCTAGGTGC | 5336 |
| rs561563960 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81826000 | TGAACTTGGAGCGAG[C/G]TCTGGAAATGTTGTC | 5336 |
| rs561565860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908006 | TTCCTGCTCTCTAAA[A/G]TGCCTGATTGGCCTT | 5336 |
| rs561580274 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950491 | GAAAGTCTTGTATAT[A/T]AGAAATCAGCAAAGA | 5336 |
| rs561601562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940811 | TCTCCTTAGCTTCTA[C/T]ATAGTTTCTCTAGTT | 5336 |
| rs561606785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811770 | TATCCAGTCTATCAT[C/T]GATGGGCATTTGGAT | 5336 |
| rs561611766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815748 | AAACCTTTGTAGGTC[C/T]TAAGTGCGCTATAAT | 5336 |
| rs561614262 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827111 | TGACCTTGCGCTGAA[A/G]TAAGACTCAGGGGAT | 5336 |
| rs561626341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850865 | GATCTCCTGCACATG[C/T]GGGCAATAGGGTTAA | 5336 |
| rs561640092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862332 | GCAAATGGTAGCAGC[A/G]GGCATTTGTTTACAG | 5336 |
| rs561649728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838377 | CAGGCATGAGCCGCC[A/G]TTGCCAGCCTGAAAG | 5336 |
| rs561651886 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864932 | TGCCGTCCTTCTCCA[A/G]AGGGATTCCCTTGTT | 5336 |
| rs561659928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913524 | GTCCGTCTCCAAAGC[C/T]TAAGCTCTTCACTCC | 5336 |
| rs561660650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824647 | TTCAGATTCAGCGGT[G/T]ATAATTAAAGGGCAA | 5336 |
| rs561668580 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821203 | GCCTGGCCACATTAC[A/C/T]CGCTTTATCAGATTG | 5336 |
| rs561670944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816910 | ACCTGGGGCCACATC[C/T]GGTTCTGCCTCTTTC | 5336 |
| rs561673631 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81801530 | TGATCTGTCCTGTCA[A/G]TGCTGGACATTTAGG | 5336 |
| rs561698032 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81814845 | CTTTGTCTCTGCAGT[A/G]GGGATTATGATGATC | 5336 |
| rs561704859 | in-del | -/A | 0.0549313 | 0.156359 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858442 | GCTACAGGGGGGAAA[-/A]AAAAAAAAAGGGACA | 5336 |
| rs561710609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787309 | TCACTGCAGCCTCAG[C/G]CCCCTGGGCTCAAGT | 5336 |
| rs561711244 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849373 | AAAATCTGGCTATTG[C/T]TGGAAGACAATGTTA | 5336 |
| rs561725223 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873927 | TATTAAGGCTAGTCT[C/G]TGTGTTTGTGTCTAT | 5336 |
| rs561726136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934331 | AAGATCCGAGTGTGC[A/C]AGAAAGCAAAGTGGG | 5336 |
| rs561733254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874256 | TCTCGCCATGGAACG[C/G]TCCACTTTCTCTGTA | 5336 |
| rs561736549 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958538 | TTAACTACCACCGGC[C/T]GCCTGCTGCAGTCCA | 5336 |
| rs561743843 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838910 | TCGGGTCCCGGTGAC[A/C]CAGTCCTCTCTTTAG | 5336 |
| rs561763294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799013 | AAGGAGGGCCCGTGT[C/G]CCTGGGGAGGCAAGA | 5336 |
| rs561766668 | in-del | -/G/GG | 0.246914 | 0.273176 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940458 | ACCTTTGGCATCTTG[-/G/GG]GGGGGGGAGTAACAA | 5336 |
| rs561767591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926509 | GATAGGGAACAATGT[G/T]TTAGCTGAATAATAA | 5336 |
| rs561781804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869818 | TGGTGGGTCTGGGCA[G/T]TAAAGCCACTCCATG | 5336 |
| rs561784027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803174 | CCCAGGCTGGAGTGC[A/G]GTGGCATGATCTCGG | 5336 |
| rs561789664 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81931307 | GACCCTACTGAATCT[A/C]CTGCATCCCTTGAGT | 5336 |
| rs561802176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893898 | AAGGTTTTAATGGAC[A/G]CATAATAACTGTGCA | 5336 |
| rs561843900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806707 | CATGAGGGTCCAGGT[A/G]TGGGGCTGGGGACAT | 5336 |
| rs561858387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840359 | GATAACTTTTCCATG[A/G]GCCAGATTGGCCTGG | 5336 |
| rs561861182 | snp | C/G | 0.00119737 | 0.0244387 | missense | PLCG2 | GRCh38.p7 | 16:81883311 | TGTTTACCTGCATGA[C/G]TTCCAGAGGTTTCTC | 5336 |
| rs561862406 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866647 | CCCTTGCTCCCAGGA[A/T]GAGCTCCACTGGGGC | 5336 |
| rs561876762 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827457 | GCTTCCCAAAGGGCT[A/G]GGATTACAGGCATGA | 5336 |
| rs561882615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810394 | ATGCTTGGCCTTCGT[C/T]ATTTGCAGCATCAGT | 5336 |
| rs561885093 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789866 | CTCCATTGCCTCCCC[A/T]CTGTCATTTGGATGC | 5336 |
| rs561898153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886750 | CCATTTATATAACAT[A/G]GAGAATAACCTGTAC | 5336 |
| rs561904038 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962487 | TTTCCACATTTCTTA[C/T]TTTTCATTAGGCCTT | 5336 |
| rs561921577 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875026 | TGGAGTGCAATGGCA[C/T]GATCTTGATTCACTG | 5336 |
| rs561923896 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825525 | GTCTCCAACTCCTGA[C/T]CTCAGGTGTTCCACC | 5336 |
| rs561937144 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886573 | AATCTAAATTTCTTT[A/C]GAGGATTGGTTAAGT | 5336 |
| rs561951684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818060 | GGGCTCGGTCACTTC[C/T]TCTCTGTCGGCTCGT | 5336 |
| rs561954859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840657 | TGAGAATCTAACGCC[A/G]CTGATGATCTGACAG | 5336 |
| rs561955676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947641 | CATAAAACCTTTGCT[C/G]AGATAGAGTTTACAG | 5336 |
| rs561982672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886383 | CATATGGAATAATCA[C/G]TGCAGCACTTTGTGT | 5336 |
| rs561984088 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81854266 | ATGCCCGGGTAGGGT[C/T]TTAGCCCTTTGTCCA | 5336 |
| rs561984743 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938125 | TCCTCAAACCCACTT[A/C]CCCTTGTCCTCTGTG | 5336 |
| rs562004574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871074 | ATGAGAATGATGAAA[A/G]CATACCATTTTCATC | 5336 |
| rs562007657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866987 | CAGCTGGCCCAACAG[G/T]GACTTTTTCTGCCCT | 5336 |
| rs562013071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848151 | GATTAGTAGAACAGG[A/G]TCAAGAGCGCAGAAA | 5336 |
| rs562018547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947243 | GAGGGAAGCTTAATG[A/C]CGGGGCTGCCACTGT | 5336 |
| rs562035067 | in-del | -/CTAA | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911597 | TGCCACTGTGCCCAG[-/CTAA]TTAATTAATTAATTA | 5336 |
| rs562048933 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888019 | CATTCCATATCAGTT[C/T]CGTTATTTGGAGCTG | 5336 |
| rs562073764 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821788 | AATGCTTTGCATAAC[G/T]TCCTACCCAAAAGAA | 5336 |
| rs562092198 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874572 | GGGCAGAGAAAAGTA[C/G/T]CTGTTTTGTGATTTG | 5336 |
| rs562096540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837908 | CCACTACCAGTCTTA[C/T]TCAGATTTTCCCCCA | 5336 |
| rs562107839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902528 | TCTGGGACATGGAGA[C/T]ATCTTTGGCCTCTTT | 5336 |
| rs562130690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841144 | ACTCTGTTGTTTATT[A/G]TCTTTTTAACAAAGA | 5336 |
| rs562170156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905798 | CTGAGTCTCTGGGAC[C/T]ACACGTGCGCACCAC | 5336 |
| rs562171968 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955470 | CATCCTCATCCTCCC[A/C]CTGCATTGAAACCCA | 5336 |
| rs562173883 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864664 | CTGGCTCATGGTAAA[C/T]ACTTGACGAATGTTT | 5336 |
| rs562176961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832867 | GCCATAAGAGAGCAG[G/T]CTAAGTGCCCAGATA | 5336 |
| rs562182062 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780450 | GCCCTCGTCCTTGAC[C/T]ACAGTTCTGCGGGGA | 5336 |
| rs562186212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880291 | GTGTACCCCAGTGGA[A/G]GTGCCTATCTCAACT | 5336 |
| rs562187245 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959188 | GATGGGAAAAGGAGT[C/G]TAACTGTGAAAAACG | 5336 |
| rs562193265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948036 | TATGGGTCCCTAATT[A/C]ACTTATGCTCCTACT | 5336 |
| rs562221496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894619 | GTCTCATGCCTGTAA[C/T]CCCAGCACTGTGAGA | 5336 |
| rs562238446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934934 | ACAGGGGAAACCACC[C/T]CCATGATTCAATTAT | 5336 |
| rs562240359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783076 | TCCAAGGCCCTCCCA[G/T]AGTGAGGGCTGGAAA | 5336 |
| rs562251722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795860 | ATGGGCCACTGTGCC[C/T]GGCCCCCTCCCACCT | 5336 |
| rs562257205 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81878610 | TACTGTCTCTTGAGT[C/G]TATTCCCGTCTTGTT | 5336 |
| rs562264835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891437 | CATCCTGCCCGTCAA[C/T]GTGATGATTCGGTCT | 5336 |
| rs562292421 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923198 | TAAGCCTAACCCTAA[C/T]CCCAGCGCTAAACCC | 5336 |
| rs562300419 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778908 | TCAGACGATCCTCCC[A/G]TCTAGGCTTCCCAAA | 5336 |
| rs562314256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855552 | TTTGAGCCTATACTC[A/T]GTGTTAGGTTGTGTA | 5336 |
| rs562324756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922262 | TGGCACTAACTCACA[C/T]TGATGGATCCAGTTC | 5336 |
| rs562352510 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796199 | ATGGTGATGTCTCTT[A/C]GACAGCCTCATCTGC | 5336 |
| rs562356261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836913 | CCCCTGCTGTGCACA[C/T]GGGCATGTACTCAGT | 5336 |
| rs562373050 | in-del | -/AG | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81920408 | CTGGAGAGGAGAGAC[-/AG]ATAATATACACAATT | 5336 |
| rs562379084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951888 | CGAGTGATCTCTATT[G/T]TATACAAATTTAAAC | 5336 |
| rs562382549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905806 | CTGGGACCACACGTG[C/T]GCACCACCATGCCTG | 5336 |
| rs562383322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848495 | TCTCTGCCTTTGTAC[A/C]TGTGCGTTTGCATTT | 5336 |
| rs562384120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890591 | ATTGCAAGCACAGAA[A/G]CAGAATGCGAAGGTG | 5336 |
| rs562392577 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81879085 | CCCTGAGTGGGGGAA[C/T]GCGGTGCGGGCTTTT | 5336 |
| rs562394196 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791438 | GAGCTCAGCTGGGCA[A/G]TTCTTCTACTCTTTG | 5336 |
| rs562394869 | snp | A/C | 0.000527741 | 0.0162355 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905548 | CACTGCGGCCACGCC[A/C]CTTGCAGCTGCTTCT | 5336 |
| rs562396703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910343 | TGATCCACCCGTCTC[A/G]GCCTCCCAAAGTGCT | 5336 |
| rs562403178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787757 | CCTACCAGACGTAAG[C/T]AACCGTTAAATTTAA | 5336 |
| rs562429212 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81864411 | TCAGCAGCCCCGTGT[G/T]GCTAGCAGCTACTAC | 5336 |
| rs562431929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825996 | GCTTTGAACTTGGAG[C/T]GAGCTCTGGAAATGT | 5336 |
| rs562441613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859005 | GAAAGTTGGAAGACT[C/T]CTCCTTTTGGTTCCA | 5336 |
| rs562445993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841008 | CTATTGAATAGTTCT[G/T]CATGAATATGAAGCA | 5336 |
| rs562456701 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891052 | CCTGTTATCCTAGCT[A/G]CTTGGGAGGTTGAGG | 5336 |
| rs562467348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938666 | GAAGGTTGCTCCGGC[C/T]TTTCCAGTGAATCTA | 5336 |
| rs562481353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904407 | CCCTCAACTTACAGA[C/T]GCTTGCCTGCGTGGG | 5336 |
| rs562487670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817666 | ATTTTTAAAATTTCA[A/G]GTAGAGATAGGGTCT | 5336 |
| rs562491606 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791686 | TCTCCCACCTCAGCC[A/C]CCCGAGTAGCTGGGA | 5336 |
| rs562491817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867042 | GGTGCTGTCCCTGTG[A/G]TACCAGTAAGTGGGT | 5336 |
| rs562519515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870647 | GAATTTGATTTTAGC[C/T]AATGTTGTAGAAAAG | 5336 |
| rs562545973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829729 | TCTTTCTTTTGAATT[A/G]CTGTAGAGCATTCCA | 5336 |
| rs562560135 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81952218 | CCAAAATTAATGTTG[C/G]ATTGGAATTGGAGGT | 5336 |
| rs562565798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866695 | CTGGCCTCTCCCTTG[C/T]TCCCAGGATGGGCTC | 5336 |
| rs562571635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806810 | GTGTTTTGAGGGCTT[C/T]AGGAATGGCCAGGAC | 5336 |
| rs562573513 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959596 | GGTGCTATCACTCCA[A/G]TTACTCCTCCAACTG | 5336 |
| rs562579054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799629 | TTTGAGACAGAGTCT[C/T]GCTCTATTGCCCAGG | 5336 |
| rs562584794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800009 | GATCTTGGCTATGCC[A/G]CTTATCCCATTTGTG | 5336 |
| rs562586553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821714 | ACAGATCAGTGGAGC[A/G]CAGAGCCCCAAAATA | 5336 |
| rs562599749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832921 | CAGGCAGCCAGTGGT[C/T]AGCCGATACTTGAAG | 5336 |
| rs562603704 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868718 | GGGCCTTTGGCATTT[C/T]TGTGGCATTTTGTAT | 5336 |
| rs562606871 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917946 | CAGGCTGGTATCGAA[C/G]TCCTGACCTCAAGTG | 5336 |
| rs562610746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925916 | AAAATCCAGAAGGAT[A/T]TCATATAGAGGGGAA | 5336 |
| rs562612046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870291 | CATAGTAGTGGTTCT[C/G]CCATTTTACAGGTAA | 5336 |
| rs562619378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855951 | TTCACACCTCTGTCT[C/G]CTTAGCCCCACCTGC | 5336 |
| rs562620850 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848065 | GCATTGTAGAACGAA[A/T]TCAGAGGACTGCAAG | 5336 |
| rs562621226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927313 | CTCTGGATCAGGGAA[A/G]ACACAGTGATGATAG | 5336 |
| rs562621278 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923216 | CAGCGCTAAACCCTA[G/T]CCCCAAACCCTAACT | 5336 |
| rs562621913 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963008 | TCTCAGCTGAGTGAT[A/G]GGCTCCCTAGAACTG | 5336 |
| rs562633861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810446 | CTCCAACTTATTTGC[A/C]ACCTGCAAACCAGTA | 5336 |
| rs562639486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934370 | AGGAAAAATGCAGGG[C/T]GAGCTGGGAAGATGG | 5336 |
| rs562640674 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81792654 | AGAAGCCTTCTTCAC[A/G]TGGTGGCAGCAAGGA | 5336 |
| rs562651312 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825311 | TTTTTTTTTTTGAGA[C/T]AGAGTCTCACTCTGT | 5336 |
| rs562660599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836597 | AATACAAAAGTTAGC[C/T]GGGCATGATGGCACA | 5336 |
| rs562666099 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906285 | CTCCAACTGGGGGTC[A/G]TTCCACCAGAAACCT | 5336 |
| rs562671657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807173 | TGAACGTGGTGATTC[A/G]TGTGGTGATTTCACA | 5336 |
| rs562672212 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953681 | CTCTTGACTAGAGTG[A/G]TGGTTCCTCAAGTCA | 5336 |
| rs562673447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794148 | AGAGGCGCCGGATTT[A/G]TGGGGAGATGCTAGG | 5336 |
| rs562698403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833309 | AAGCTTCTGGAGGAC[A/T]GGGGCCTTCTTTCGC | 5336 |
| rs562701616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815214 | GGGAGGAGGTTTTAT[A/T]GCATATGGGGCCTTA | 5336 |
| rs562711746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796222 | TCATCTGCCCTCTTG[C/G]GTTTCTCTCACAGAT | 5336 |
| rs562723959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947702 | CACCTTCTGAAGAAG[C/T]CATTTACATGTCACA | 5336 |
| rs562724353 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787233 | TTAAAACAAAATTAA[-/T]TTTTTTGAGACAAGG | 5336 |
| rs562746444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822169 | AGCTTTGTCAATTGT[A/G]GTGGGGTGTGGGGGA | 5336 |
| rs562752117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939618 | CAAACAAACACCTCC[C/T]CCGTTCCCTTGTCCC | 5336 |
| rs562761247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836933 | ATGTACTCAGTGTTT[C/T]TGTGCATGTGGTTTC | 5336 |
| rs562784323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848515 | CGTTTGCATTTCTCT[C/T]CCTCCTTGTCTGGGT | 5336 |
| rs562794471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871716 | TTAAAAATTAAGAGG[G/T]TGTATGTTTTGATCT | 5336 |
| rs562806141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874650 | GAGCTATTTATGGTG[A/G]CTTATAATCCCCAGA | 5336 |
| rs562807236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938985 | TGTGGGAGTGCTCTT[C/T]GTGGGGGATTTTGCA | 5336 |
| rs562807329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867401 | TTGTGTGAGCTACTC[A/G]CTTGGAGGCAGTCAG | 5336 |
| rs562820057 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962627 | ATGTTGGCTGTTGTT[A/G]ATGTGAAAATTAAAC | 5336 |
| rs562833874 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895604 | CATTGAAACTAGCTT[G/T]TCTTGGACAGCTGCA | 5336 |
| rs562854860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848973 | TAACCAGACTAAGAA[C/G]ATTTTCAGTGGTGCC | 5336 |
| rs562871103 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81795640 | CAGAGGATGGCTCAG[C/G]AGGTTGGAGGTTTCT | 5336 |
| rs562878558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874805 | AAGTTTGGCAGCAGC[A/G]GGAGGATAAGAAATG | 5336 |
| rs562883890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871400 | CTGGAGTGCAGTGGT[A/G]TGATCTTGGTTCACT | 5336 |
| rs562892829 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822473 | TTTTAAGAAAAAGGC[A/G]GGGCTGGGGGCAGTG | 5336 |
| rs562893466 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81954298 | AGTGCTGGGGATTAC[A/G]TGCCTGAGGCACTGC | 5336 |
| rs562915023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802090 | CCTTCAGGTGAGTAC[A/G]GTCTTTTTTTTTTTT | 5336 |
| rs562921193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872801 | CTGCTCCTAGCCTCA[G/T]TCTTCTCCTCTGTGC | 5336 |
| rs562923568 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837562 | TCGTGGGTGCCATGG[C/G]AAAGCGTTAACAACA | 5336 |
| rs562926774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956156 | GGCATCGTGTGATTT[A/G]TGATCTTTTAGAGTT | 5336 |
| rs562928635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951519 | TAAATAACGTAATTC[C/T]AATTTCACTCCACCA | 5336 |
| rs562938649 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857497 | ACAATTCTGGGGGCT[C/G]GGAATGCCAAGATCA | 5336 |
| rs562939099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826055 | TATTTCAAACTCAAC[G/T]TGTCCAAAATGGAAT | 5336 |
| rs562945336 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81846930 | GCAAACAATTCTCCA[C/T]TGGACACCAGTTTGG | 5336 |
| rs562947795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782768 | AACGATTCTGTTAAA[A/G]TGGGGCACAGGCAAA | 5336 |
| rs562950713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899598 | AAAGCTTCAACAAGT[A/G]TCCTCACCATCTGTT | 5336 |
| rs562962872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902812 | TATGGCTGGGGAGGC[C/T]TCACAATCATGTCAG | 5336 |
| rs562964954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877805 | TGTAGATGTCATTGC[A/G]TCGCTCCTTGGCTTG | 5336 |
| rs562971609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880643 | TGAATATCCCTAAAA[C/G]AAATTCTAGAAGGAA | 5336 |
| rs562976221 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801696 | TTTAATTTTTTTTTT[C/T]TTGAGGTGGTGTCTT | 5336 |
| rs563014438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943650 | CCCAAGTCAGAATCT[C/G]CATTTTAACAAGATT | 5336 |
| rs563026663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928836 | CTGTAAGTGCTAAAA[C/G]AAGGTCTCGTACATA | 5336 |
| rs563045009 | snp | A/C | 0.000422551 | 0.0145292 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919464 | CTTGGCATGTCAACC[A/C]TGTGTTCTTCCTGCT | 5336 |
| rs563076515 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780179 | AGGGGTGACATGGCG[C/T]GAGGGAAACAGGTGG | 5336 |
| rs563101058 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910883 | GTTTCCAAATTCCTG[C/G]CACCATGACCTGTGT | 5336 |
| rs563105191 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841506 | TCGGCCTCCCAAGGT[G/T]CTGGGATTACAGGCA | 5336 |
| rs563105890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943827 | GCAGTATATTCAATG[A/G]GAGCAATGTCCCCAT | 5336 |
| rs563114771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876253 | GGCTTGAACTCCTGG[C/G]CTCAAGTGATCCACC | 5336 |
| rs563124655 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923978 | TGAGACTTTCCAAGT[-/CA]CACAAATAAATACTA | 5336 |
| rs563136779 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910316 | GGCTGGTCTGGAACT[C/T]CTAATCTCAGGTGAT | 5336 |
| rs563148987 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781493 | TGCATCTTTGTGCAT[G/T]TCTTTCTTTACATGT | 5336 |
| rs563152452 | snp | A/C/G/T | 4.96927e-05 | 0.00498443 | missense | PLCG2 | GRCh38.p7 | 16:81891512 | AAAACAGCATCTGGG[A/C/G/T]TGAGAAGTATGACGC | 5336 |
| rs563154292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941582 | TTTTTTTTTTTTGTA[C/T]TCTAGAAATGTTCAT | 5336 |
| rs563162470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816395 | ATAAATTAGGCTTCA[C/G]ATACTGAACTATCTG | 5336 |
| rs563162711 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81876623 | TTAGTTTATCTATTA[C/T]TTTAGTCACTCATCC | 5336 |
| rs563168223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869649 | TTTTGGAAAATATTA[C/T]GAAAGATTCCTTGTG | 5336 |
| rs563179479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818452 | GATGACTAGCACATA[C/G]CAGGTAGACCATAGA | 5336 |
| rs563180199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853925 | CCTCTTATTATTATT[G/T]TTAATTTGAATCAGT | 5336 |
| rs563190014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919878 | CATTTAAAATATCCA[C/T]AGCATGTGCCAGATG | 5336 |
| rs563203474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879104 | GTGCGGGCTTTTTCT[G/T]TGCTTTGTTGAAAGG | 5336 |
| rs563204700 | snp | C/G | 1.65831e-05 | 0.00287945 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869338 | AATTTTATGAATGCG[C/G]AGTGACTTAGCCTCT | 5336 |
| rs563226688 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81810958 | GTTATGCACCTGAGA[A/G]GCAGCCCAGGGAACA | 5336 |
| rs563227970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846772 | AAAAGGTTTTTTTCA[A/G]TTCACATTCAATACA | 5336 |
| rs563229447 | in-del | -/ATT | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892740 | AGGTTTGCTGTGCAG[-/ATT]ATTTTGTCACCCAGG | 5336 |
| rs563255413 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838274 | ATATTTTTAGTAGAG[A/T]TGGGGTTTCACCATG | 5336 |
| rs563262505 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822192 | GTGGGGGATTGAGAT[G/T]TGGCTTTCCTGGGAA | 5336 |
| rs563265345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798037 | GGTTCCACCATGTTG[A/G]CCAGGCTGGCCTTGA | 5336 |
| rs563309892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917383 | TTTCTCTTTGACATA[C/T]TGATTTCCTTTCCTT | 5336 |
| rs563321093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897180 | GAGGCCATCATATGC[C/T]GACTCCTGGTTTGGG | 5336 |
| rs563321115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901164 | GGAGACAGCCCCATG[C/T]GAGGTGCTGGAGGTG | 5336 |
| rs563334258 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882976 | CCCCATGGCCACACT[C/G]CTGGAGGGGCTCCTC | 5336 |
| rs563350718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945816 | GGAGGAAATGGATGA[A/G]GATTCACTACTCTTT | 5336 |
| rs563359542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876067 | GTCTCACTTTGTCAC[C/G]GAGGCTGGGGTGCAG | 5336 |
| rs563360804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938031 | TAAACGATCCCCATT[C/T]AGGCAGTGTTTGAGG | 5336 |
| rs563367277 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777295 | CCATCAAGAGACTTA[A/G]CCCACTCCCCTATCC | 5336 |
| rs563377778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853637 | CTGACAGTTGGTGGA[A/G]CTCAGATAATAGTGC | 5336 |
| rs563386949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794420 | TGAGGGTGGTCCCCA[A/G]GCCCCTGCAATGAAG | 5336 |
| rs563392832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957545 | GGGTCAAGATCCCCC[A/G]ACAGGGATGCTTGTG | 5336 |
| rs563397122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942296 | TGTGTCAATTCATCT[A/G]CAGAATGCAATGACT | 5336 |
| rs563399430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912847 | ATCAGCGACAACAAC[A/C]ACCACCACAGCAAAA | 5336 |
| rs563400317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878954 | GCTTCCGGTTGCTTC[A/G]ACAAGCAGAGTGTCC | 5336 |
| rs563411127 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888599 | AATGCTTCACAGAAA[C/T]TGTGTGGTAGATACT | 5336 |
| rs563417435 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921766 | GAGGAAGAACCACAG[C/T]GAATTTTCTGTTTGG | 5336 |
| rs563456976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873317 | AGGAAACTGTAACAA[A/C]CACAACAAAAACCAT | 5336 |
| rs563462025 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886874 | ATTTTCATCCTTATT[C/T]TTTGCCATTTTCACT | 5336 |
| rs563473638 | snp | C/T | 6.62405e-05 | 0.00575464 | missense | PLCG2 | GRCh38.p7 | 16:81937806 | CTCTCAATGGGCGCA[C/T]GGGCTACGTTCTGCA | 5336 |
| rs563475370 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81928455 | AATGCATTTTAAACA[G/T]TTCCACAGGCAGTAT | 5336 |
| rs563482306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839593 | TTTAAACTTAATTTT[A/G]TATAGAAAAGAAACT | 5336 |
| rs563500717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847278 | CTGGGCATGCCACCC[A/G]CCAGAAACTTCCATG | 5336 |
| rs563501459 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778083 | AAACACACACACACA[A/C]AAAAAACGCTATAAC | 5336 |
| rs563502119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820685 | GAGTGCAGTGGCGCA[A/G]TCTTGGCCCACTGCA | 5336 |
| rs563503759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843256 | CTCCTTGACCATCAT[C/T]TGCCCATCTCCTTCT | 5336 |
| rs563504446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894255 | GCGACATGGTGAGAT[C/T]GTATCATTACGAAAA | 5336 |
| rs563505368 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81811979 | GAACTGATTTACACT[A/C]CTACCAACAGTGTAA | 5336 |
| rs563515907 | snp | C/G | 1.65877e-05 | 0.00287986 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81893733 | AGGTGACCAGCTGCG[C/G]AGCGAGTCGTCCCCA | 5336 |
| rs563522596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865711 | CCAGCATGAGAGGAC[A/G]CTGGCCTCTCCCTTG | 5336 |
| rs563551734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809729 | TCTTTCTCCTCTTGC[A/C]CCTGATTGGCTAGCC | 5336 |
| rs563575876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893415 | TTTTTTTGCTTCTGA[C/T]GTGCTTTGACCAACT | 5336 |
| rs563586859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955371 | TCACTTGAACTCCAT[C/T]GGGAAAGGCCAATTG | 5336 |
| rs563588886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898416 | AAAAGCTTTTTAGCT[G/T]TTATGTTCTAGTAAG | 5336 |
| rs563592327 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777745 | AACAGGCCGGGTGCA[C/G]TGGCTCATGCCTGTA | 5336 |
| rs563592664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835926 | AATTTCCCTCTTACA[A/C]GGACAGTAGTCTTGG | 5336 |
| rs563618824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861887 | AGAGATCCATCTTCC[C/T]ATCGGCTGGTCCAGG | 5336 |
| rs563633724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929265 | GGGACTCTGTAGCGG[A/G]CCTCCTTGTTCTGGG | 5336 |
| rs563638300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854415 | AGGGAACTCCAGCTT[C/T]TAATTGGCTCATGTT | 5336 |
| rs563640553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879767 | GCAGGGTGCCTGTGT[A/G]CAATGCACAGAAAAT | 5336 |
| rs563647175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819853 | CCTCCCAAAGTGCTG[A/G]GATTACAGCTGTGAG | 5336 |
| rs563653132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839978 | AGGAGGGTCCCTTGA[C/G]CCTACGAGTTCAAGG | 5336 |
| rs563656907 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866053 | CCAGCATGAGAGGAC[G/T]CTGGCCTCTCCCTTG | 5336 |
| rs563676677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828215 | CTTGTGAAGTCTGTT[A/C]CAGACTGTTGAGAAA | 5336 |
| rs563681529 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81914622 | GCACCTACTGTGTGC[C/T]GGGCCCTGTGCTGGG | 5336 |
| rs563681944 | snp | G/T | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960879 | GCAGTGTTCAGAGCC[G/T]CATCTTCCTGTTATA | 5336 |
| rs563687791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879552 | TTCCCTTTCTAGAAC[C/G]CTGATAGTCCCCATG | 5336 |
| rs563697940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836167 | TCAACTAGTGTTTTC[A/G]TACCCTAGAGACTAT | 5336 |
| rs563698302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800962 | ATGGAGGAAGGGGCC[A/G]TGAATCAAGGAATGC | 5336 |
| rs563703613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921885 | TTTTCAAAAATTTAT[A/G]ATCCATGGCCAATGC | 5336 |
| rs563719635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798818 | AGGTGGAGGAGGGGC[C/T]GGCCTCCCCGGCCTC | 5336 |
| rs563722323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933307 | TTTTGCGGAGCTGGT[C/G]TTGGGGAGCAAAGGA | 5336 |
| rs563729880 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931907 | TGAGTGCCTGCAGCA[A/G]TGCTCATTGATGATG | 5336 |
| rs563739012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825023 | CAAGAAATGCAGGTG[A/G]CCTCTAGAGCTGGGA | 5336 |
| rs563768098 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809816 | TCAGCAGAGTCAGGA[-/T]TTTTTTGGCCGGGGC | 5336 |
| rs563781185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913028 | AGCAAGATTAAGTAA[C/G]TTGCTGAAGCATGCA | 5336 |
| rs563793348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790803 | GTAGGGGGCATTTGG[C/T]AAAGTCTGGAGACGT | 5336 |
| rs563795527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785936 | CTCTTTAATTCTGCC[C/G]TTTCAGCTTCCTGAT | 5336 |
| rs563803645 | in-del | -/CACACA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896421 | ACACACACACACACA[-/CACACA]AATCATCTGGGTGTA | 5336 |
| rs563819556 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850947 | GTCTGCAATCAGTGG[G/T]AATGGCCCTTTGAAC | 5336 |
| rs563821445 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854329 | CAGAGATAGCTTTGC[A/C/G]GGATCCTGTTGGGGA | 5336 |
| rs563822584 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951479 | TAGGATCTAGATGGT[C/T]TTATAGCTTAGTTTT | 5336 |
| rs563835077 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799815 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 5336 |
| rs563840465 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806888 | GTGATGGGGGCAGAG[G/T]TATGGGGAGGAAGCA | 5336 |
| rs563840736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926471 | AGATGGATTATGTCC[C/T]GTGTTGTTAGTGTTG | 5336 |
| rs563841407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861576 | CGCCACGCTGGGCCA[C/T]CCTCTCGTGTTACTG | 5336 |
| rs563843060 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799133 | TTCTCCTAATTAAAA[C/G]AACTGCTTTTTCCCC | 5336 |
| rs563849710 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873976 | GGAATCAGAGTTTTA[C/G]AAAATGTCAGAACCC | 5336 |
| rs563857380 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81799840 | CCTCGTGATCCTCCC[A/G]CCTTGGCCTCCTAAA | 5336 |
| rs563876866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925476 | GTGAAAAGGGCTTAC[A/T]ACCCGCAGTCCTGTG | 5336 |
| rs563887604 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853046 | CTTAAGTATTAGGCC[C/T]CAGGCTGGGCCCGCT | 5336 |
| rs563899267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813394 | TCCTTCACATCCCTT[A/G]TAAGTTGTATTCCTA | 5336 |
| rs563905257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873448 | TCATAGAATAATGAT[A/G]ACAGTGTGCGTATGA | 5336 |
| rs563906757 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802636 | GAGTGCAGTGGCGCA[A/T]TCTCAGCTCACTACA | 5336 |
| rs563912870 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934205 | TGTGGCCAGGACTGA[A/G]CTGCACACCAAAACC | 5336 |
| rs563920764 | snp | C/G | | | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961999 | CGGCTGATCTGGCTG[C/G]CTAGGTGGGTGTCCC | 5336 |
| rs563959678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866620 | CACTAGCATGAGAGG[A/G]TGCTGGCCTCTCCCT | 5336 |
| rs563985787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851246 | CTGTGAACCATTCAT[C/T]TAGCTGCTCCAGTGA | 5336 |
| rs563991110 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901538 | TGGGGTTTCACAGAC[A/C/T]CCCGAAGAATCCACG | 5336 |
| rs563998236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866150 | GAGCTCCAACTGGGG[C/T]ACCAGCATGAGAGGA | 5336 |
| rs564007743 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81955185 | AATCATCTTCTGTCC[C/T]CCTTCTCCAAAGTCA | 5336 |
| rs564009949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876798 | TAGGTAGAATCTGAC[C/T]ACATAACCCTCCATG | 5336 |
| rs564027030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917870 | GGGACTACAGGTGCC[C/T]GCCACTGCGCCCAGC | 5336 |
| rs564032092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802173 | GCCAGAGTGCAGTGG[C/T]GCTATCTTGGCTCAC | 5336 |
| rs564032689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901613 | CATCTTTATTTGTTT[A/G]ACCTGTACATAAAAC | 5336 |
| rs564039885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937268 | GCACAACTGAGAGGT[A/G]AAAACTGATACATCG | 5336 |
| rs564044060 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958481 | CCATAAGGGCCCAAA[C/G]AGAAGCCCTACCCAC | 5336 |
| rs564049856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950411 | GCATAGTACCTAAGT[A/G]TATAAGACAAAAATT | 5336 |
| rs564050259 | in-del | -/ACAC | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781048 | CAAACAAACAAACAA[-/ACAC]ACACACACAAACACT | 5336 |
| rs564058627 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942276 | TACCTTAATGGGCAT[C/T]AAAGTGTGTCAATTC | 5336 |
| rs564064336 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81836290 | AGGTAGTGGCAGTGG[C/G]ACTGGATCGTGGATC | 5336 |
| rs564082424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824584 | CTTCTCACCATGTTC[C/T]TCGTGTGCCACACTG | 5336 |
| rs564089105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945886 | ATCACTACACTCAAT[A/G]TGGAATGTTCTGTGG | 5336 |
| rs564089959 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777831 | GACCAATCTGGCCAA[A/C]ATAGTGAAACCGCGT | 5336 |
| rs564110526 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81899345 | GTATATATGTATATA[C/T]ATGTACTAATGATAT | 5336 |
| rs564114306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786359 | TGAGGTTTACACCAG[A/G]TGGAGGAAGTTCAGC | 5336 |
| rs564117989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820339 | CAGCATGCACACTCC[A/C]TGCCCCAGGCCACCC | 5336 |
| rs564123066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877194 | GCACGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 5336 |
| rs564123162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880104 | ATATTAGCCGGGCAT[A/G]GTGGCGCATGCCTGT | 5336 |
| rs564123708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954314 | TGCCTGAGGCACTGC[A/G]CCCGGCGACTTGATT | 5336 |
| rs564141797 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828067 | TGCACTCCAGCCTGC[C/G/T]CAACAAGAGCAAAAC | 5336 |
| rs564151220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913507 | GGTTCAGATGCAGGC[C/T]TGTCCGTCTCCAAAG | 5336 |
| rs564153633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934227 | ACCAAAACCTCGTGG[A/C]AACAGCTTTGTCGAG | 5336 |
| rs564154778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847018 | ACAGGTTGAGAGCTC[A/G]GTCCCTCAAGACTCT | 5336 |
| rs564176732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873061 | GATCATTGAATTGCA[A/T]TGTGTTCATTTTTTC | 5336 |
| rs564177909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790820 | AAGTCTGGAGACGTG[C/T]TGATTTTCTCACCTG | 5336 |
| rs564186753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953908 | TTTTGAACTTGCGCC[C/T]GAATAACAAATACCC | 5336 |
| rs564191697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946335 | GAAACGGCCCGTGAA[A/T]ACAATTGGCAGATGG | 5336 |
| rs564202727 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827888 | CTGAGGTCGGGAGTT[C/G]AAGTCCAACCTGATC | 5336 |
| rs564209798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816858 | AAGAACTGAAAGTGC[A/G]GTTGCGCTGTTATCA | 5336 |
| rs564213144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879781 | TACAATGCACAGAAA[A/G]TGGGCTGGTGCAAGT | 5336 |
| rs564230052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810053 | CTGGAGTTCAGTGGC[A/G]TGATCTCAGCTCACT | 5336 |
| rs564243082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81843658 | GTACATAGGATACTA[C/T]ACAGTAATGTTTCTG | 5336 |
| rs564266589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933814 | GGGGAGGCCCAACAG[G/T]GTTGCCTGCTTTGGG | 5336 |
| rs564266837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938586 | TCAGGTGGCATATGG[C/G]GCCGAGACCCAGGCT | 5336 |
| rs564268074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840331 | TTTGGCACCAGGGGC[C/T]GGTTTTGTGGAAGAT | 5336 |
| rs564269891 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803782 | TACCTCCTGGATTCA[A/C]GTGATTCTCGTGCCT | 5336 |
| rs564273575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820742 | CCTCCCACCTCAGCC[C/T]CCTGAGTAGCTGGGA | 5336 |
| rs564295961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791373 | TCCTGTGGGATTAAT[G/T]GGTGTCATGTAATAT | 5336 |
| rs564299386 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81881662 | TATAGTATGTATATT[C/G]GAGACGGAGCCTCCC | 5336 |
| rs564301286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890658 | CTTGCATAGGGAAGG[A/T]GGGGAGGTGGAACTG | 5336 |
| rs564314117 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802614 | TTTCACTCTTGTCGC[C/T]GGGCTGGAGTGCAGT | 5336 |
| rs564320521 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798687 | TGTGAAGGATTCTGT[G/T]TTGAGAAAGAAGGAA | 5336 |
| rs564349604 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806265 | TGCATTACCTGCTTC[C/T]GTGGTCCCCAAGCAG | 5336 |
| rs564359315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870172 | GAGATGGGAGAAGCA[C/T]TTACCATTGATTGCT | 5336 |
| rs564378941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832320 | GGAATAATCCTCAGA[G/T]TAAGCAAAAGAGGTT | 5336 |
| rs564382550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951404 | TAAAGAATGTAAATA[C/G]GCTAAAATTGTTCTG | 5336 |
| rs564382650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946822 | GTGGGATCAATTAAT[G/T]TAGCTGAATGGTAAA | 5336 |
| rs564394201 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951005 | GGCCAAATTTTGTTT[G/T]GAGACAGTGTTTTTT | 5336 |
| rs564395653 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913128 | TCTGGTTTCCTCCCA[A/C]CTGCAGCTGCTGCCC | 5336 |
| rs564397043 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889624 | CCCTTTCAGAGGCTG[C/G]AGTTTCGTTTTTTTA | 5336 |
| rs564410876 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825390 | GTCTCCTGGATTCAA[G/T]CCATTCTCTTGCTTC | 5336 |
| rs564436587 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778792 | CCTGGCGGGTAATTG[C/T]GAAGAGTATATTTAT | 5336 |
| rs564444048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877317 | AAAAATTAGCTGGGC[A/G]TAGTGGCGGGTGCCT | 5336 |
| rs564449451 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81951428 | TGTTCTGAAAAGCAG[C/T]AGAAAAGTTAAAACA | 5336 |
| rs564450954 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902252 | GAGCTCATGGGGAAG[A/G]ACAAACAGCTGTTTC | 5336 |
| rs564479911 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855183 | GGGTGACAGAGCAAG[A/G]CTCTGTCTCAAAAAA | 5336 |
| rs564498064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832852 | GTGGGTGACCCATTA[A/G]CCATAAGAGAGCAGG | 5336 |
| rs564512511 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858829 | CTAAATCAAAGTCCT[C/G]TACTTTTTACTATTT | 5336 |
| rs564513157 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81889820 | CCACCATGTCTGGCT[A/G]ATTTTTTTTGTATTT | 5336 |
| rs564527231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905008 | TCTTACTGTCTCAGC[C/T]TCCTGAGTAGCTGGG | 5336 |
| rs564529533 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81949868 | GTATGCTAAAGGTTA[C/T]TTCAACTTTGACGAC | 5336 |
| rs564532625 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881589 | CTTTTCCCTCTGTCA[C/T]TTTTGAAATCAGAAA | 5336 |
| rs564557688 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962434 | CAAAATATTTTCTTT[A/T]TGAAGAGCCAGATTC | 5336 |
| rs564569455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881167 | CTGGGAGGATGGTCC[A/G]GAAAGTTCTGTAGAA | 5336 |
| rs564582171 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781996 | CCTGCCTCAGCCTCA[C/G]GAGTAGCTGGGATTA | 5336 |
| rs564590016 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898948 | CCAGCACTTTCGGAG[C/G]CTGAGGCGGGTGGAT | 5336 |
| rs564595050 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958932 | TGGAGCAGCAAGCTG[A/G]GCTTTAATGGGCTAA | 5336 |
| rs564596862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782255 | GAAAAACCTTTAGAA[A/G]GACATGAAATGTAAA | 5336 |
| rs564617213 | in-del | -/AA | 0.00582746 | 0.0536635 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916298 | CTTTTTTAAAAAAAG[-/AA]AAAAAACAACGTTTT | 5336 |
| rs564625599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842760 | ATGGGAGCTTGAAGA[A/G]CAGGGTCATGGCCCG | 5336 |
| rs564626404 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81825299 | TTTTTTTTTTTTTTT[G/T]TTTTTTTGAGACAGA | 5336 |
| rs564628254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848459 | TAGAATTTCATTCTT[C/T]CTTTCTTACCATGCT | 5336 |
| rs564632677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923146 | AAATTGAGCAATATT[G/T]TGTCACTACAATATA | 5336 |
| rs564633233 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811366 | AGGGATGGTTTTGCA[A/C]GTCGGGGTTCAGGAC | 5336 |
| rs564634570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918504 | ACTTATTTAACAGAC[C/T]GTCCTTTCCCCCTGG | 5336 |
| rs564641653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955420 | GCCAAGCTTCACAGA[C/G]TAGTCAGGGATCCTC | 5336 |
| rs564656063 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81868859 | TCACCCTATACTGGG[C/G]ATCTCCAGTGTAGGT | 5336 |
| rs564663046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895179 | AAATTTCTCATTGCT[C/G]TGTATCATTTCCACG | 5336 |
| rs564672532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935892 | TTTGTGTTTTCTTGT[C/T]CAAGGATGGTGATAG | 5336 |
| rs564672850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922820 | ATTTATGCCCGCCAG[A/G]CAGAAAGCATGAAAG | 5336 |
| rs564674530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940179 | GAATCACTGTAAAAC[C/T]GATTGGGTGGCTTGG | 5336 |
| rs564687493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927674 | CTCCACCAAGGATGA[C/T]ATCTTTGTAATGAGG | 5336 |
| rs564699023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892474 | GACATTCCAGGGGGT[C/T]ATCTGGGAAAAGGCT | 5336 |
| rs564713826 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809740 | TTGCCCCTGATTGGC[C/T]AGCCTTGTCACTTCT | 5336 |
| rs564734110 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81924027 | GCGCTTTCCAATACA[C/G]AAGACTGTGTGTTAT | 5336 |
| rs564750190 | snp | A/T | 3.43359e-05 | 0.00414328 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931460 | TTGTGGCCCTCTAAT[A/T]GGCTGATTGGGACAT | 5336 |
| rs564754148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884851 | AATGAACCACCACGT[A/G]TCATCACTCAGATTA | 5336 |
| rs564766206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903253 | TGTACCCTATATTAT[C/T]ACTGGGCCACCAAGA | 5336 |
| rs564767670 | snp | C/T | 0.000132573 | 0.00814058 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869317 | AGTTTCATGGCTCAG[C/T]CTGGGAATTTTATGA | 5336 |
| rs564788104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896648 | AAAATTCCCCTTCTG[C/T]CCTAATTCCCTCTTT | 5336 |
| rs564806241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803106 | ATACATGGCTTTTTG[A/C]ATTTCACTTTTTTTT | 5336 |
| rs564811385 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960247 | GGAAAGGCACACATG[A/G]TATGATGGCTCTTCC | 5336 |
| rs564834888 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828937 | TTCTGATTTTACAGG[A/C]GATCACAGAATGAAT | 5336 |
| rs564841554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878625 | CTATTCCCGTCTTGT[C/T]TCCATCCCTGCCTCC | 5336 |
| rs564853629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957069 | TTTGGGAGGCTGAGG[A/G]GGTTGGATCACCTGA | 5336 |
| rs564866579 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805590 | CAACCCAATTAAAAA[C/G]TGGGCGAAAGATCTG | 5336 |
| rs564868159 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826836 | GACTCTCAAGGCTGC[A/C]GGAGACAATTTTGAG | 5336 |
| rs564872882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903579 | CAAAATAGCTGCAGC[A/G]CTGTTTGCACCCAGG | 5336 |
| rs564873782 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794385 | TCTCGCTGGCATCTC[C/G]TAAGAAGAAATCCAT | 5336 |
| rs564890749 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778615 | CTGGGGTTCTTTGCT[C/T]CTGACTCCCTTTGGG | 5336 |
| rs564891184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830140 | GCCTGGGTAACATGA[C/T]GAAACCCTGTCTCTA | 5336 |
| rs564910538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875879 | GCATGGGGGAAGTGA[C/G]TGATGAGCGTTCTGT | 5336 |
| rs564916440 | in-del | -/T | 0.485324 | 0.0843964 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787394 | GCCTGGATAATTTAA[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs564925088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807887 | TCAACAGCCAGATCT[C/G]TCAAGAACTCACTGA | 5336 |
| rs564925783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911502 | GAGTGCAGTGGAACA[A/G]TCACGTCTCGCAGCA | 5336 |
| rs564925880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906991 | TTCAGTGAGCTGAGA[C/T]TGAGCCACTGCACTC | 5336 |
| rs564946735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927008 | ATTGAGCCAGCAGCC[A/G]GGTGCAGATGAGCAG | 5336 |
| rs564970591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842681 | GTGTCAGGGGTGGGA[C/G]GACGTTCCGTGGGTG | 5336 |
| rs564974526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948718 | CACAAAGGCCCTCCT[C/T]ATGCCTCATCAGCTA | 5336 |
| rs564986239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911172 | ATAAAGAAAAAACAA[G/T]TTTTAGGCAGAAAGC | 5336 |
| rs564991847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860045 | GCACAGTCATAGCTC[A/G]CTGCAGCCGTAAAGT | 5336 |
| rs565007503 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81880436 | AAGATAGAGAAATAG[A/G]CACACAGGGACACTT | 5336 |
| rs565010144 | snp | C/T | 3.32303e-05 | 0.00407603 | missense | PLCG2 | GRCh38.p7 | 16:81910681 | TCGAGCTGCGGCTCA[C/T]GGACCCTGTGCCCAA | 5336 |
| rs565019050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928372 | CTGGCACCCTCTCCC[C/T]GCCAGGTCCCTATCA | 5336 |
| rs565027089 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873144 | GCTTGGGAGTTGGGA[G/T]AACTGGATTCTAGAC | 5336 |
| rs565037381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924894 | CCCAGTTCAGAGGCT[C/T]GGCTTTGCCGAAGTC | 5336 |
| rs565052373 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81857240 | GGTGGGACCTAAGTA[C/T]TGGGGTTTTGAAAAG | 5336 |
| rs565068977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872189 | AAAAATTAGCCAGGC[A/G]TGGTGGTGTGCACCC | 5336 |
| rs565070727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949025 | AGAATAGACCTGATT[G/T]GTTGCATTAAAAAAT | 5336 |
| rs565087198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823823 | GCATGAACCACTGCA[C/T]CCAGACAATTCTTTT | 5336 |
| rs565095339 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781375 | GTGCACCATTATTTA[A/T]CCAGGAGGCCCCCCA | 5336 |
| rs565117253 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81862400 | TCCTTAGGATATGCT[C/G]TTGGCTGACGGTTGA | 5336 |
| rs565133854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849911 | ACTGGCAGTCAACTG[A/G]GTGGGTGAATAACTA | 5336 |
| rs565136522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781916 | TTGCTCTGTCGCCCA[G/T]GCTGGAGTGCAGTGG | 5336 |
| rs565143660 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945434 | GGCAATCTTGGGAAA[C/G]ATACTGTTAACCATG | 5336 |
| rs565151945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900349 | TTTAAAGATATGAAT[A/G]GATGGAAAAAAATAC | 5336 |
| rs565181536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800932 | ACTGGAAGATGGCAC[C/T]AGCTGGCTCTGAAGA | 5336 |
| rs565186546 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793941 | CTGTGTTGTTTTCTT[C/G]TCCTAAATGATCTCA | 5336 |
| rs565186823 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81821872 | GACAGATCCAAGATG[-/T]TTTTTTTTTTTTCCA | 5336 |
| rs565201081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781611 | TCTCACTTGCAGTGG[C/G]TGACACCATTCCTTT | 5336 |
| rs565213877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780890 | AAATTACCTGGGCGT[C/G]GTGGTGGCCGCCTGT | 5336 |
| rs565217700 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888879 | TGCCCATTTGCCTAC[A/G]GATCATCTGTGGCTG | 5336 |
| rs565221214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819720 | CTCCTGAGCAGCTGG[C/G]ATTACAGGTACCCAC | 5336 |
| rs565232155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928066 | TTCATCTCAGCCAGA[C/T]CCTGGGATGGTTCAA | 5336 |
| rs565236361 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885316 | GGTGTGAGCCACCAC[A/G/T]CCCAGCCCCGACTAA | 5336 |
| rs565242821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871487 | GGGATTGCAGACGTG[A/C]GCCACCACGCCCAGC | 5336 |
| rs565257693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839513 | GCCTTAATAATTTTT[A/G]TTATATTTGCATACC | 5336 |
| rs565289686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940853 | TGGATCTTTCCCACT[A/G]GATTTTAGGTATAAT | 5336 |
| rs565302049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865293 | AGCCGTTGGCTTCCT[C/G]CCCTGCAGCGATGGG | 5336 |
| rs565319747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888855 | CAAAATATTGTTGGA[A/G]TACAACCATGCCCAT | 5336 |
| rs565320726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896097 | CTCACCCGAGTGTTG[A/G]CACCCCCTGCAGGCC | 5336 |
| rs565326546 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81886443 | CTTTGGCTGTATGCA[A/G]TGAAAAGAAAGCTTT | 5336 |
| rs565329609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823218 | TTCAGCCTAGGGGAG[A/G]TCTGGCTTCCCCGGG | 5336 |
| rs565333172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831512 | TTTGTCTCAGTTTTA[C/T]ACCTGGGGACATGGT | 5336 |
| rs565346332 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944864 | CCATAGATATCAAGG[C/G]CCAACTGTAGAGTAA | 5336 |
| rs565368643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916587 | ACTTAACCATTTTTT[G/T]TTTGTGTGTGGTGAG | 5336 |
| rs565373430 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822561 | CAGCAGTTCGAGACC[A/G]GCCTGGCCAATATGG | 5336 |
| rs565392860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822895 | GGCCACGATTGCAGG[C/T]GGCCACTGCAAGGTG | 5336 |
| rs565409836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875345 | TGCCATTTTAGGGAT[G/T]AAGAAACTGAGGTCC | 5336 |
| rs565439598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928898 | CCAGCGTCACTCTTA[C/T]TATTTCAGGATCCAT | 5336 |
| rs565447107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875033 | CAATGGCACGATCTT[C/G]ATTCACTGCAACCTC | 5336 |
| rs565449130 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878328 | CTGGATTCGGGTCCA[A/C]CCTAACCCAGCAAGG | 5336 |
| rs565452882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885590 | GCGTCATTTTGTTTG[C/T]AAATACTTCTGTATG | 5336 |
| rs565497974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885121 | AATGGCTCTGTCCCA[C/T]GTTCAAGTGATTCTC | 5336 |
| rs565499865 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81945423 | ACATATGCATAGGCA[A/G]TCTTGGGAAAGATAC | 5336 |
| rs565505939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882384 | GTTAATTTTGCCCTG[A/G]TGGCCTGGAGTCTGG | 5336 |
| rs565509336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896698 | CACCAAACCTGTTTC[C/T]ACAGGCGGAATCCAA | 5336 |
| rs565516760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897298 | AGCAGTTACGAGTAT[A/G]GGTTCTGAGTCCTTC | 5336 |
| rs565528737 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883435 | GTGCTCACCTGGTCA[A/C/G]CTGTGCTCACCTGGC | 5336 |
| rs565531025 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831213 | TATTGACTTGTCTCT[C/G]TCTCCTCCTATTAGA | 5336 |
| rs565535814 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871132 | TGACAGAGCTGTGGG[C/G]AAAATGTAGAGAAAT | 5336 |
| rs565540981 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808926 | CATGAGCTTGGTGTA[G/T]TTTGTGGCCTATTGG | 5336 |
| rs565564104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838122 | CTGGCTCTGTTGCCC[A/T]GGCTAGAGTGCACTG | 5336 |
| rs565575210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800980 | AATCAAGGAATGCAG[A/G]TGGCTTGTGCAAGCT | 5336 |
| rs565581335 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81834711 | TCTGAGCAGGGTGGG[C/G]AGGAGAACCCACTGG | 5336 |
| rs565593688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882172 | ACATACCCATTACCC[C/T]GGGAAGCCCCGTGTA | 5336 |
| rs565608342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860933 | AGTGAGCCGAGATCG[C/T]GCCACTCTACTGTGG | 5336 |
| rs565613869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937177 | AGAGATCGTGGGCGG[C/G]GATGCAAATAGGTGG | 5336 |
| rs565613963 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865627 | GATGGTTCCTTTGCC[C/G]TGCTGCTGTCTGGGC | 5336 |
| rs565617564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853069 | GGCCCGCTGGCTCAC[G/T]CCTGTAATCCTAGCA | 5336 |
| rs565637474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804543 | ATACATTTTAACCAT[C/T]ACTTCTGCTTTTTTT | 5336 |
| rs565651029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797249 | GTTGGGGGAGGGATC[C/T]AGTTAAAGATGTCCC | 5336 |
| rs565651567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948750 | AGTTGGTCAGTTTGC[C/T]TAATGCTGGCTCCAA | 5336 |
| rs565654709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871842 | GGCAAAGTACCTGGG[C/T]ACCATCTGAATGTCT | 5336 |
| rs565676802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896342 | AGAGCCTGGGCAACA[C/T]GGTGAAACCCCTTCT | 5336 |
| rs565700465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838659 | AAATACCTAATGCCT[C/G]CAGGGTTTAAAACCT | 5336 |
| rs565716765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789566 | AGTGCTGGGATTACA[C/G]ACAGGAACTACCATG | 5336 |
| rs565767671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882023 | GGAAAGGTTAGAATT[A/G]TACTCATAATCAAAG | 5336 |
| rs565780421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826511 | ATAGTAGGACCTATC[C/T]CACAGCAGTGTTTTA | 5336 |
| rs565785907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842400 | TCCCAGACTCGGAGC[C/T]GTCTGAGGGCAGGAC | 5336 |
| rs565799851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903320 | GGTTTGGTAGGGAGA[C/T]AAACCCGTCAACAGA | 5336 |
| rs565802969 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81850332 | GTCTGTAAAAGTACT[A/C]AAGCTTCCCCCAGAT | 5336 |
| rs565813291 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961249 | TGAACAAGGATCAAC[A/C]TCTCCATAAATGAAA | 5336 |
| rs565837710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834751 | TGGCTGCCCTTTACA[A/T]GGGCTCCCAGGACGA | 5336 |
| rs565847462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936599 | GCAGGCTTCGTGATT[C/G]TAAGTAAGTGACAGA | 5336 |
| rs565847801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784980 | GAGCAGAGGAGTGAC[A/G]TGATTTGATTCATGT | 5336 |
| rs565856889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885341 | GACTAATTTTGTATC[G/T]TTAGTAGAAACAGGA | 5336 |
| rs565869761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811511 | TCTCCTAGTGCTATC[C/T]CTCCTCTAGTCCCCC | 5336 |
| rs565886801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847059 | AGGTGCCAGTCACAA[A/G]CCCAAGTTGTGGCCT | 5336 |
| rs565889548 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81898102 | TGCTTTGAGAGTTTG[C/G]TTTCATTTGCAGGAC | 5336 |
| rs565898887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853743 | GGTCACAGAGACAAC[C/G]TGGATTGAAGGGCAG | 5336 |
| rs565900072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865047 | AGGGTCATCACCCTG[C/G]GGGAAGGAAGGCAGC | 5336 |
| rs565922068 | in-del | -/GTTTTTTTGTTC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81874955 | CCTATGTGTTTTTTT[-/GTTTTTTTGTTC]TTTTTTTTTTTTTTT | 5336 |
| rs565935364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864708 | TTGCTACAAAAGAGC[C/T]GGGGGCAGTGGAGGT | 5336 |
| rs565952963 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81915544 | TTCTCTTTTCTCCCA[C/G]GGAAGTTAGTTGTGG | 5336 |
| rs565966366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846374 | TTTAGCTTTATTCTG[C/T]TCGCCATCCCACTCC | 5336 |
| rs565976693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882209 | TGTACTCCCCATCCA[A/G]CCCGGGGGTGGCTCG | 5336 |
| rs565978335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842151 | TGGGGAGCATAAGCC[A/G]GGATTTGAACCAAGG | 5336 |
| rs566005609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936913 | TTCCACAGAATGGAA[C/T]AATCATTTATTTAAT | 5336 |
| rs566027415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801573 | ATGATACTCCCGATT[C/G]CAGCAAACACGTCTT | 5336 |
| rs566040075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805302 | CAGGAGATCGAGACC[A/G]TCCTGACTAACACGG | 5336 |
| rs566041849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827256 | CAGTGGTGCCACTAT[C/T]GCTCACTGCAGCCTC | 5336 |
| rs566058018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781654 | TTCCCTCTAATGCTG[C/T]AGGGTGGGTGTAAGG | 5336 |
| rs566072806 | snp | A/G | 1.65707e-05 | 0.00287838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928526 | ATTATTCCCGTTACA[A/G]CTAACGTGAGTTATG | 5336 |
| rs566100100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921580 | TCGCTGACAGAGCCT[G/T]TGGTGTTTATAAATT | 5336 |
| rs566101611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805091 | TTCCCCAATCACCAT[G/T]TGCCAGAAAACCTTT | 5336 |
| rs566105337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830910 | AGGGGAGATGGACAG[G/T]CACTGCGGGTCATGA | 5336 |
| rs566108217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893527 | CAGAGCTCATGCCCA[C/G]TGTGACCGTGGGATT | 5336 |
| rs566146798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932104 | AGACCCGGTTCTTTC[C/T]GGTGGAGGAACTTCC | 5336 |
| rs566151807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892636 | AAACCTAGAAGACAG[C/T]TAAGAAATACAAACT | 5336 |
| rs566162132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925535 | TCCTCACTCTGCTTA[C/T]TCAGACCAAAAAATT | 5336 |
| rs566163058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808533 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 5336 |
| rs566184025 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782870 | ATCAGAGGGGATACA[C/G]TGTTTTCAAAGGAAC | 5336 |
| rs566186535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897676 | TCAGCCTCCCGAGTA[G/T]CTGGGATTATAGGCA | 5336 |
| rs566204755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954049 | ATTTTTTGAGACAGG[G/T]TCTCATTGTCTTGCC | 5336 |
| rs566207981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860745 | GGAGGCAGAGGCAGG[C/T]AGATTGCCTGAGCTC | 5336 |
| rs566215589 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842850 | AGGGGCCAAAAGTCC[C/G]CAAGGCTGTGCCAGA | 5336 |
| rs566232738 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836347 | GTCAGCCATGGACTC[A/G]TATTCCCACTGGTGG | 5336 |
| rs566239808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869031 | GACATTGCTTGAGCC[G/T]TGCTCATTGAAGTGT | 5336 |
| rs566243034 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962305 | ACTTTTTGAACCCAA[C/T]CGTAAAAGCTATCTT | 5336 |
| rs566255641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824342 | TTTCACCACGTTGGC[C/G]AGGCTGGTCTTGAAC | 5336 |
| rs566270635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820067 | CTGTGAAGATGTCCT[A/G]TTTCATCTTTAAGGA | 5336 |
| rs566274308 | snp | A/T | | | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963121 | CCCCCAGTGGTTGGA[A/T]TAGTTACCCTGGTCC | 5336 |
| rs566296896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795953 | GCATGCTAGAAGAAC[A/G]GGGCCTAAGTTGGGG | 5336 |
| rs566300977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831567 | AACCCCATACTCCAG[C/T]TGGGACCCCTGGCTG | 5336 |
| rs566304673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803026 | ACTTTACTTTCCCCC[A/T]TCCCTGGCAATGACA | 5336 |
| rs566306122 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81839458 | TAGCCTATTAAAATA[C/T]TAATAGGCTGTATAT | 5336 |
| rs566306745 | snp | C/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959320 | ATGCTGGGCTTAGTA[C/G/T]GCATGTACTGCTGAA | 5336 |
| rs566320415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897315 | GTTCTGAGTCCTTCT[C/T]GCTGAGTTTGAATCC | 5336 |
| rs566323910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949794 | ATAAAAAATGACAAT[C/G]AAAAGCTAAAAAATA | 5336 |
| rs566336315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949306 | GGTGAGATGAATAGA[A/G]AACACATCCATACCC | 5336 |
| rs566339012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819930 | GTCTTATTTTCCATT[A/G]TCAGAGAAATGCAGA | 5336 |
| rs566347930 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855035 | GCCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA | 5336 |
| rs566353340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923062 | GAGCTTCTGGGAGGC[A/T]TGCTGAGCACCGGCA | 5336 |
| rs566384558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832579 | GTGTGTGTGTATGTA[C/T]TTTTTGTGGAGATGG | 5336 |
| rs566393279 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81813246 | AATAGCATTGAATCT[A/G]TAAATTACTTTGGGC | 5336 |
| rs566395805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925215 | CCGCCCAGCGGCTGT[G/T]GTCAATTCCTCTCTC | 5336 |
| rs566403019 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81849797 | AAAAAAAAAAAAAAA[-/A]CCAAAAAAATTCCCT | 5336 |
| rs566436540 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911645 | GACCGGGTCTCGCTC[-/T]TGTCTCCCAGGCTGG | 5336 |
| rs566442824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832954 | CTCCTGTGTGCCCAG[C/G]TTGCTGCTGGGGCCA | 5336 |
| rs566447536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902336 | GGTTATAAACAACAG[A/G]AACTGATTTCTCACG | 5336 |
| rs566452397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909619 | CTGGAGTCTCACTAC[A/G]TTGCCCAGGCTGGTT | 5336 |
| rs566464202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883179 | AGTGGGGCGTTCTGG[A/G]TGGCAGGCTGCCCCA | 5336 |
| rs566474914 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81887366 | CCTCATGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 5336 |
| rs566484508 | in-del | -/A | | | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778032 | AAAAAAAAAAAAAAC[-/A]AAAAAAAAAACAAAA | 5336 |
| rs566499206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883422 | CCTTCTGCCGCCTGT[C/G]CTCACCTGGTCACCT | 5336 |
| rs566522478 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789281 | TTTCACTCGCTTACG[C/T]GGATGCGCTCTCTCG | 5336 |
| rs566524858 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938685 | CCAGTGAATCTAGGA[A/T]AATTAGGGCTGGCAT | 5336 |
| rs566533748 | snp | C/T | 1.67489e-05 | 0.00289381 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870849 | CTTTTTTCATATTTA[C/T]AGGAAATAGGAGCAC | 5336 |
| rs566543183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863580 | GAAGCTGAATTGCTG[A/G]ATCAGTTGCTGGATT | 5336 |
| rs566560777 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810206 | ATCTTGGCCAGGATG[A/G]TTTCTATCTCTTGAT | 5336 |
| rs566563088 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802019 | CCAAAAAATCTGTGG[C/T]TGTGCAGAGGTGCCC | 5336 |
| rs566564141 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914117 | CGCTGCACACGGATT[G/T]AAAACCTGCTGTGTG | 5336 |
| rs566601529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862512 | TTGTCAGGGGTGGCA[C/G]CAGGGTTTGCAGACT | 5336 |
| rs566606300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899021 | GGTGAAACCCTATCT[G/T]TAGTAAAAATACAAA | 5336 |
| rs566606851 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81802886 | ATTGTATACCCTATA[A/G]TGTACCCCTTAATGT | 5336 |
| rs566611968 | snp | A/G | 0.000198761 | 0.009967 | missense | PLCG2 | GRCh38.p7 | 16:81919528 | TCAACCGGGACGGCC[A/G]GCACTTTGTGCTGGG | 5336 |
| rs566620805 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923252 | CCCCTAACCCTTAAC[C/T]CCAACCCAGGTACCC | 5336 |
| rs566625330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874403 | TCACTGCATTTTAAA[A/T]ATTTAATTTAGTGAC | 5336 |
| rs566628296 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789587 | AACTACCATGCCCGG[C/T]CTCAATTCATTCTTT | 5336 |
| rs566630003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895373 | AGACCACCCTGGCCA[A/G]CATGGTGCAACCCTG | 5336 |
| rs566630263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791933 | GTCCCAGGCAGAAGC[C/T]ACAGGCTTCTTACGA | 5336 |
| rs566643602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874690 | AGGGAGTGGGTTCAT[A/G]CTTATCAGCAGCCAA | 5336 |
| rs566664546 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826126 | TTCCTCCAGTTTTCC[C/G]CATTGTGGTAAGAGA | 5336 |
| rs566687814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926570 | GTACTAGGTAGGCGC[C/T]GTCCCAAGCACTCAG | 5336 |
| rs566701385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951587 | AAGCTATACAACTTT[C/T]ATATCAAAACTGGAG | 5336 |
| rs566719834 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865020 | GTGTGCAGGAGGCTT[A/G]CTAGGGAGTGCAGGG | 5336 |
| rs566722658 | snp | C/G | 4.97113e-05 | 0.00498529 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81910640 | CATCCAGCACTACCG[C/G]GAGACGCACCTGCGC | 5336 |
| rs566723046 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878067 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 5336 |
| rs566747338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807664 | AGGCATAGCCCAGGG[G/T]CACTGTATTAGTCTG | 5336 |
| rs566747817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955970 | TCAATGGTTTATAGC[C/T]TATTACGTGTTGTAC | 5336 |
| rs566762795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951208 | CTGCTCTCAGATCCT[C/T]CTGCCTTAGCCTCCC | 5336 |
| rs566769679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867901 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 5336 |
| rs566779327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877413 | TGAGCCGAGATTGCG[C/T]CACTGCACTCCAGCC | 5336 |
| rs566791995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855331 | CACTTTCCTCACTTT[A/C]CTCAGGGGCAGAAGC | 5336 |
| rs566794335 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81842939 | TGAGGCTGACTCTAG[C/G]AGACTCAGTGTGTGG | 5336 |
| rs566794411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939248 | AGACACAGAGAGAGG[A/G]GGTGAACCTACGTGG | 5336 |
| rs566806825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943312 | GGGAGGCCTCAGGAA[A/G]TTTACAATCCTGGTA | 5336 |
| rs566809302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807370 | CTTCTCAGATCCTGG[A/G]CTCTGCCTTCTGGAT | 5336 |
| rs566816614 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81919289 | CTGAGACACAGATTC[C/T]TCTAGATCTGTTTTG | 5336 |
| rs566836347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837182 | CGAGAATACATATAC[A/G]TGCAGTGCTGCTTCA | 5336 |
| rs566839042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939646 | CCCTGATCCTGGGGC[A/G]GGGAGATGGGAGGTG | 5336 |
| rs566839072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788126 | AACTCAGTTTCATCA[C/T]TTTAGGAACTGTCAG | 5336 |
| rs566839300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914692 | GCTCTCTCAGGCTAA[C/T]GGTCTGGCAGGGATG | 5336 |
| rs566854480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864033 | ATGGCCTCTGGCGTT[A/G]CAAATTTTTTAAATA | 5336 |
| rs566861844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814586 | TGTAATCCTAGCTAC[A/T]CGGGAGGCTGAGGCA | 5336 |
| rs566862628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810865 | GCACAACATTGATCA[A/C]ATAATTTTGTACATG | 5336 |
| rs566869936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852156 | GATAACACTTTCTTC[C/T]ATGGTAGACAAGGTG | 5336 |
| rs566878715 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817879 | AGCTCCCTGTGCTTA[C/T]GAACATGTTCTCACG | 5336 |
| rs566894055 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856461 | CTTATTAACAAGGGT[A/T]ATAGCAACCATGGGT | 5336 |
| rs566906370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841249 | TTATTTATTTATTTA[C/T]TTATTGAGATAGAGT | 5336 |
| rs566917969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779808 | GCCCTTGTGCCCAGA[A/G]CTCGCGGACGCTCGG | 5336 |
| rs566918317 | snp | A/T | 1.65677e-05 | 0.00287812 | missense | PLCG2 | GRCh38.p7 | 16:81891536 | ATGACGCGGTGGACA[A/T]GCAGGACATGAACAA | 5336 |
| rs566919442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829355 | TTCAGGTGATCTGCC[A/C]GCCTCGGCCTCCCAA | 5336 |
| rs566947541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927517 | TATATTGGACAGCCA[A/G]ACATTGAGAACGTGC | 5336 |
| rs566952500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891316 | TGCAGCCTGAGCCTT[C/T]GGTATTGAAAACGTG | 5336 |
| rs566958251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902643 | TCTACCCTCATTCCC[A/G]TTCATAAAAGCTCTA | 5336 |
| rs566982231 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829189 | TCTCGGCTCACTGCA[A/T]CCTCTGTCTTCCGGG | 5336 |
| rs566984211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833400 | CCTGAGCCAGTATTC[G/T]GGCCCGGGGTGGCCG | 5336 |
| rs566985218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947387 | ACATCTGTCACCTGG[C/T]TCTGTGCCACTCACA | 5336 |
| rs566988044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857035 | TCATGCAACCAGTCT[A/G]TTTTAGACTTCTGGC | 5336 |
| rs566988177 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844753 | AGATAGTGAGAATTT[G/T]CATAGTGATGGACAC | 5336 |
| rs567058268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856134 | TTGATTCACATTCCA[C/T]CTTCTCACTTACTGG | 5336 |
| rs567066354 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877703 | GTGTAGATGGCATTG[A/C]TCTTTGGTGTGCAGA | 5336 |
| rs567068695 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81890559 | AGAGGGCATCTGCCA[C/T]CAGGGAGAGTTGAAC | 5336 |
| rs567069662 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788441 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 5336 |
| rs567074133 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845659 | AAGGTGGCTTGAATG[C/T]ACTGCGTTGAGCGCA | 5336 |
| rs567089788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814978 | GAGATGGTGGCGATA[A/G]GAAGTTACTTTTATT | 5336 |
| rs567090354 | snp | C/G | 0.000430492 | 0.0146649 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880965 | TGGGGTGAGGCAGCT[C/G]TTGTGTGTCGTTCGG | 5336 |
| rs567101347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903003 | GTTCCTCCTATGACA[C/T]GTGGGAATTATAGGA | 5336 |
| rs567107394 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960292 | TGCTACATAACTTCA[A/G]TATCTAGCTGAGACA | 5336 |
| rs567109551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799834 | TCCTGACCTCGTGAT[C/T]CTCCCACCTTGGCCT | 5336 |
| rs567114075 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779107 | TTTCTTCTTTGGCAC[A/G]CAGAGGCGGGGCTCC | 5336 |
| rs567126773 | snp | A/G | 0.0024537 | 0.0349404 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895756 | GGGGGCTGACCTCGG[A/G]GCTGTCAGTGAACAC | 5336 |
| rs567126793 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81907871 | GTGGCTTCTCTGGCC[A/G]GCTGGCAAGGGGATG | 5336 |
| rs567151447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906683 | CCCGCCTTGGCCTCC[C/T]GAAGTGCTAGGATTA | 5336 |
| rs567156261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851977 | GGCCACGAACCTCTC[C/T]TGTGTTTCACTATGA | 5336 |
| rs567161977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910905 | GACCTGTGTCCTTTT[C/G]TCTTTTCTTTCTTTC | 5336 |
| rs567165104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845242 | CATTGTTCCCTGTCC[C/T]GTGTTATTTCTTATG | 5336 |
| rs567166818 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849146 | TTAGTCCTTACAGCA[A/G/T]TGGGACGTCACGGGA | 5336 |
| rs567169334 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845820 | GACTTTGCTGAATAC[C/G]AGATAGAAAACCCTG | 5336 |
| rs567171606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833534 | CAAAATTTAAAAAAA[A/T]CTTTTTTTTTTTTGA | 5336 |
| rs567174150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884088 | GGGTAGGGTGGCTCA[C/T]GCCTATAATCCCAGC | 5336 |
| rs567178713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877438 | CCAGCCTGGGCGACA[C/G]AGCGAGACTCCGTCT | 5336 |
| rs567183314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899639 | TTTTTCCTGTTTTTG[A/G]GCTTTTTCTTGGTGA | 5336 |
| rs567223003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852275 | CAGGAGGATGCTGAT[G/T]GTGCAGCTGGGCCAT | 5336 |
| rs567230695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803745 | GGAGGGCAGTGGTGC[A/G]ATTTTGGTTCACTGC | 5336 |
| rs567238171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855432 | AAATACGATTAAAAT[A/G]GACCAAAGTGGGTGA | 5336 |
| rs567244795 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899391 | CACGTTCACATGATA[C/T]AGAAGGATACAGGTG | 5336 |
| rs567260786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905650 | GTGAATTTACCTTCC[G/T]TCTTAAACTTTATTT | 5336 |
| rs567280582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880360 | GTGCCTACAATGTGC[C/T]GTGTCTACGCGCTTT | 5336 |
| rs567288151 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81953475 | GGTGGGGGAAAAACT[G/T]TATTTTTTTGTGTAT | 5336 |
| rs567295659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911243 | GCAACTTTTTTTTTC[A/G]CTTTTTCTGTCACAT | 5336 |
| rs567303381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841296 | GGCTGGAGTGCAGTG[A/G]CATGATCTTGGCTCA | 5336 |
| rs567320244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894724 | CTAAAAATACAGAAA[A/T]TAGCCAGGCGTGGTG | 5336 |
| rs567337142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859860 | TTCTAAGGGCTGGTA[A/G]AGATGTGTTGGGTGA | 5336 |
| rs567350190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891367 | CGCCTGTTGATTTCC[C/T]GCATCAGAGCTGTTC | 5336 |
| rs567353057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806925 | ACATGACCCAGGGCT[C/G]TGGAGGCCTCCATAG | 5336 |
| rs567357131 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859421 | TGGACCTCATCACAA[A/G]TATTTGAGCACCTTT | 5336 |
| rs567358116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822720 | GAACCGAGTTCATGC[C/T]GCTGCACTCCAGCCT | 5336 |
| rs567367793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788471 | ATTTTTAGTAGAGAC[A/G]GGGTCTCACTGTGTT | 5336 |
| rs567372750 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG2 | GRCh38.p7 | 16:81963105 | GACCCCCAACCCCCA[A/G]CCCCCAGTGGTTGGA | 5336 |
| rs567374916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783320 | ATTATTATATTATTA[C/T]TATGCTTTAAGTTTT | 5336 |
| rs567386915 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832604 | AGATGGGATTTTGCC[A/G]TGTTGCCCAGGCTGG | 5336 |
| rs567399692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810519 | GAAAAATTTGGGTCA[C/T]CCATTCACACATGCC | 5336 |
| rs567406563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915468 | TGGCCGTGGCATCCA[C/T]GCTCCAGGAGGATGG | 5336 |
| rs567421892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891657 | GTTGAGGCAGGGGTC[C/T]GATACGCCGCTCCGG | 5336 |
| rs567428933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792799 | CCCACTGGGTCCCTC[C/G]TATGACACATGAGGA | 5336 |
| rs567438111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895492 | TTCAACCCGGGAGGC[A/G]GAGATTGCAATGGGC | 5336 |
| rs567444784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871465 | TGCCTTAGCCTCCCC[A/G]GTAGCTGGGATTGCA | 5336 |
| rs567454217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779681 | CCGTGCGGTGGGGCG[A/G]CCCCAGCTTTGAATG | 5336 |
| rs567468977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951624 | AGTACTCCTAGCTTT[C/T]CCCTAACCTCATTCA | 5336 |
| rs567477899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928176 | TGCTTCCACAGGACA[C/T]GGGGAGCCACAGAAG | 5336 |
| rs567479863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801002 | GTGCAAGCTGGAAAA[G/T]GCAAAGGAACTCATT | 5336 |
| rs567484981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796427 | AGTATCCTTTGGCAC[A/G]GCCAGCCTTTCCTGG | 5336 |
| rs567492806 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843826 | TGAAAGAAGAACTCA[A/G]TAGAATGGGCAGGAT | 5336 |
| rs567495272 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779229 | GGGGCGAGGCGGGGC[C/G]AGGCTGGGCGGTGCG | 5336 |
| rs567523353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947444 | CTGGGATGAAGAGTC[A/G]CTCTTGGAAGCCGAG | 5336 |
| rs567524109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822457 | TGTGTTCACAGGGTC[A/C]TTTTAAGAAAAAGGC | 5336 |
| rs567538878 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81942691 | AATTCTGAGCACTTT[A/G]AGGCCGAGAGACTAT | 5336 |
| rs567541026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927858 | TACAGTCTAAGCAAA[A/G]GTGTGGCAGTGGGAA | 5336 |
| rs567569275 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822640 | CGTGTACCTGTAATC[C/G]CAGCTACTCAGAAGG | 5336 |
| rs567585257 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909211 | ATGAAAAAGCAGTCA[C/G]TCAAATGATTTGCAA | 5336 |
| rs567585372 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81808199 | ACCATTCATTTAAGC[A/G]TTTGTGACTACATTT | 5336 |
| rs567586858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826189 | AGCTAGAGTCCTCCT[C/T]GGCCCCTTTGCCACC | 5336 |
| rs567596231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888267 | CCAGGCTGGAGTGCA[A/G]TGGTACAACCTCGGT | 5336 |
| rs567602682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804312 | TGCTCATTGCTCTAT[C/G]TTAAATAGTTGATGT | 5336 |
| rs567609991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856533 | TGCTGTCCCTCTGTG[C/T]CATCTTGATTAGAAG | 5336 |
| rs567614695 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81809961 | CTCTTCATCTTTCTG[C/T]CAGTCTTTGTCTGCC | 5336 |
| rs567618953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884493 | TTACCAGCTGCACAG[C/T]CACCGACAGGTGGTT | 5336 |
| rs567629789 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81870109 | CCCCCAATATTCCAC[A/G]TTAATCCAATAATAG | 5336 |
| rs567649500 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81943644 | AGACTTCCCAAGTCA[A/G]AATCTGCATTTTAAC | 5336 |
| rs567669976 | snp | A/G | 1.66651e-05 | 0.00288657 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940092 | TAAGATGTTCGATTT[A/G]GGCTGGCGTTGTACT | 5336 |
| rs567700299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837694 | CATGTGTTTTTTTTT[C/T]TTTTTTTTCTCCTTG | 5336 |
| rs567702738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864163 | GGAGGCTGCTGGGCT[C/G]CATCTCACAGTGGCT | 5336 |
| rs567722641 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81856014 | GTAAGGAGACCAGAA[A/G]AACCCGGGTCTTGGA | 5336 |
| rs567726363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853430 | AACCTTTTTGGTACC[A/C]GTGACCAGTTTCATA | 5336 |
| rs567730287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814997 | GTTACTTTTATTATT[A/G]TCAGGACTGCTTGTT | 5336 |
| rs567742484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887845 | GCATGGAGAGGAAAG[C/G]AACAGTTACTTAATA | 5336 |
| rs567747062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878735 | GTCCACTCAGCAGCA[C/T]GTGTCAAAGCTGGTC | 5336 |
| rs567750821 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795997 | GCTTTTCTGTAACCC[C/G]TAATTTTGGAGGGTA | 5336 |
| rs567763563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790489 | ACTGTCAGTGTCACC[A/G]CTCAGTCTCCTGCTG | 5336 |
| rs567763860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841559 | AACTTTACTTTTTGC[A/G]AAGTTTTTTTTCAGA | 5336 |
| rs567783978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931987 | TTGAATATTTTCTTT[C/G]TAAGTATCATATAAA | 5336 |
| rs567790395 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818547 | ACGGAAATGGAGCTC[C/T]GAAGGCCTGAGCTTC | 5336 |
| rs567797255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917516 | CAGTCCCACCCACCA[A/G]GTGCAGGGGTCCCCT | 5336 |
| rs567813820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849675 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATCACTTG | 5336 |
| rs567823654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794547 | TGTCAAATCCTGGTC[C/G]TGCACTTGGTAGGGG | 5336 |
| rs567834353 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81871321 | TGAGGAATTATATAT[A/G]TGTTTCTTCTTTTTA | 5336 |
| rs567846937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807915 | TGAATATTGCAAGGA[C/T]AGCACCAAGAGATGG | 5336 |
| rs567847746 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81858388 | TGTTGATTTGCGTAG[C/T]TGCTGATTCCTTTAT | 5336 |
| rs567852673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853176 | TCTCTACTAAAAATA[C/T]AAAAACTAGCCGGGC | 5336 |
| rs567858570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917100 | TCTACTCTCCACTTC[C/G]GTGAGTTTAAACCTT | 5336 |
| rs567876150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802446 | TTCATGTCTGTACTT[C/G]CAGCTTTTGCTACCA | 5336 |
| rs567884930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784891 | TGGGGGCAGGCAATG[C/T]GTTTCTGGGGATTTG | 5336 |
| rs567919914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929325 | GGCATGCTCCCCTAG[A/G]ACTCAGGTGACAGCA | 5336 |
| rs567925964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867675 | CCTTTTGCCTGGGAC[A/G]TGTTCTCCCTTGCTT | 5336 |
| rs567938712 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926862 | TTAAGATCATGTGAT[-/G]GGGGTAAAATCAGCC | 5336 |
| rs567940520 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960768 | AATCTAAACTTAAGT[C/G]GCCATGGCCAGTGGC | 5336 |
| rs567951605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912129 | GTAGAGACAGAGTTT[C/T]GCCATGTTGGTCAGG | 5336 |
| rs567955046 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956961 | CGGGCCAGGCTTCTG[G/T]AAAGCCCTCTGAGTT | 5336 |
| rs567969771 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954197 | GGCTAATTTCTTTCA[-/T]TTTTTTATAGTAACA | 5336 |
| rs567972111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942203 | GGATGAGGGCCTTGA[C/G]CCTCATAACCCCTCC | 5336 |
| rs567973397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881253 | GGTTAATAGTTTTTT[G/T]TTTTAATTACAAAAA | 5336 |
| rs567975950 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801980 | GCCATCACACCTGGC[C/G]AACATTTCATTTTGA | 5336 |
| rs567981735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834343 | TGCTGGCTGCTGGCA[C/G]AATTGTGAGGGCGGT | 5336 |
| rs567983703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829857 | GATGGGGAAGGAACC[C/T]CTGAGTGGGGGGGCG | 5336 |
| rs568002959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858121 | CATGACGGTGTGAAA[A/G]GGGATGCTTTCTTTG | 5336 |
| rs568004367 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824248 | AAGCAATTCTCCTCC[C/G]TCAGCCTCCCAAGTA | 5336 |
| rs568014169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886083 | ATTATTCAGTTTAGT[A/G]GGGAACGATTAAAGT | 5336 |
| rs568016899 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865824 | CCAGCATGAGAGGAC[A/G]CTGGCCTCTCCCTTG | 5336 |
| rs568023829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81908774 | TCACTTCGGCACTGT[A/G]ACCCAGATTAATGAG | 5336 |
| rs568046771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81933445 | ACCTCATTGATGGCA[C/G]AGGGCAGTCACAAAA | 5336 |
| rs568051769 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81913367 | TGCCTTCAAGGCCTC[A/G]TCTGATTGAATCCTT | 5336 |
| rs568063678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866206 | ATGAGCTCCACTGGG[A/G]CACCAGCATGAGAGG | 5336 |
| rs568096101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942637 | TCTCTTTTAATCCTC[A/C]CAGTAATCCTGTGAA | 5336 |
| rs568100260 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946974 | TTTGTGCATCTATTG[C/G]CCGGGGAAAGGGAAC | 5336 |
| rs568105052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885849 | ATGAGGATGTTGATG[A/C]GTGTTGTAATCATCA | 5336 |
| rs568105404 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777957 | GGGAGGTGGAGGTTG[C/T]AGTGAGCCGAGATCG | 5336 |
| rs568106252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821356 | GGCATAGTGGTGAAT[A/G]CTGGAGGTATTTCCA | 5336 |
| rs568110018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869393 | GAGTTCCGTGGAATA[C/G]TGCACAAGAAAATCC | 5336 |
| rs568126123 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851391 | TCTTGTTATTTTGCA[A/T]TTGTTTTGGTGTGTA | 5336 |
| rs568127939 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816506 | TTTTTGAGACACGGT[C/T]TCATTCTGTTGCCCA | 5336 |
| rs568134086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945927 | CTTCTGAGTGAATCA[C/T]TTTTATTTCTAGATG | 5336 |
| rs568139798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828383 | CCTGGGACTACAGGT[A/G]CCTGCCACCACGCCC | 5336 |
| rs568165173 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851759 | CTCAAGTGATCTGCC[A/C/T]GCCTTGGCCTCCCAA | 5336 |
| rs568167928 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778186 | TTCAAGAACAGCCTG[G/T]GACACATAGTGAGAC | 5336 |
| rs568170930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820987 | GTCTAGAACTCCTGA[C/T]GTCAAATGATCCGCC | 5336 |
| rs568175815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816133 | CCCAGCACTTTGGGA[G/T]GCTGAGGCAGGAGGA | 5336 |
| rs568189201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874029 | CGTGTGGAACTTTGT[A/G]TGGCAAAGATTCTGC | 5336 |
| rs568201457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839603 | ATTTTATATAGAAAA[A/G]AAACTTGATTTCATA | 5336 |
| rs568210099 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922379 | CATACTCATATAACT[A/G]CTTACCTGTTATGGT | 5336 |
| rs568214233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854947 | TGTACGCTGGGCTCA[C/T]CCCTGTAATCCCAGC | 5336 |
| rs568214914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802747 | CAGCTGATTTTGTAT[A/T]TTTAGTAGGGACGGC | 5336 |
| rs568225448 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877221 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCGC | 5336 |
| rs568243972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879848 | TTGGTGGAAGAGCCT[C/G]TTCATCATGCAACAG | 5336 |
| rs568263121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904668 | TGTTGTTGTTTATTC[A/C]CCGAGTATCAACAGA | 5336 |
| rs568263204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939142 | CTGTAACTCAAGTCC[A/G]GAATCGTAGGTGAGG | 5336 |
| rs568279598 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882769 | ACCCCACCTCATTCT[G/T]GCTCACCCCACCTCG | 5336 |
| rs568281138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954574 | CCCACTTATGAGTGA[A/G]AACATATGGTATTTG | 5336 |
| rs568283471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782066 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCATCGTGT | 5336 |
| rs568294490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901693 | CTGTCACCAGCAGAA[A/G]TCATGAGTGTTTTCA | 5336 |
| rs568296421 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958976 | ACAGAAAATTTCAAA[C/T]GCAGCCATCTCCCTT | 5336 |
| rs568301070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782412 | TTTTTGAAAAAACCA[A/G]AAAAAGCAGAAGCAA | 5336 |
| rs568321163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789212 | TGGGCATGAGACAGG[A/T]TTTTGGCTTGAAATC | 5336 |
| rs568322814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831981 | AGCGGAAGGGACTGA[C/G]TTCTGCAGGCTGCTG | 5336 |
| rs568329415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809816 | CTCAGCAGAGTCAGG[A/G]TTTTTTGGCCGGGGC | 5336 |
| rs568339845 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962147 | CTCCCCTGCTGGAAC[C/T]TCCAAACAAGCTCTC | 5336 |
| rs568350394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870389 | GTTCTGTCTGACTCC[C/T]AATGCTTTACAAAAT | 5336 |
| rs568357421 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81861655 | TCTCTTTCAGCCTCG[A/G]AGGTGATGCCTCTTC | 5336 |
| rs568361081 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958692 | AAAGCCCATCAGAGA[C/G]ACCAGAGCCGTGCTG | 5336 |
| rs568363769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786436 | GAAATGGCATTCAGG[A/C]AGCTCTCCTTGCCTG | 5336 |
| rs568381002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817763 | GAGAGCTGGGGTTAC[A/T]GGCATAAGCCCCTGC | 5336 |
| rs568382462 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922501 | TTTATCATTATACAC[A/C/G]TGATCTCATTTAGTA | 5336 |
| rs568384445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813113 | TCAGGTAGCATGATG[C/T]CTGCAGCTTGTTCTT | 5336 |
| rs568394357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795137 | AAGTAGTGAACAGGA[C/T]CCTGAAGATCTCTAG | 5336 |
| rs568408440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894827 | GCAGTAAGCTGAGAT[C/T]GCGCCGCTGCACGCC | 5336 |
| rs568412766 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795528 | GGGTGGGACTCTGCT[A/G]TCTGATCACAATGGG | 5336 |
| rs568417473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844222 | ATGGTCTCTATCTCC[C/T]GACCTCGTGATCCAC | 5336 |
| rs568423576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918102 | TTTTGGATATTGACC[C/T]CTTACCAGATGTTCA | 5336 |
| rs568424495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950708 | ACAAAAAGATGGCAA[A/C]ATTGCTCACAATTTG | 5336 |
| rs568438842 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81833766 | TGCCTAGGCTGGTCT[C/T]GGAATTCCTGGGCTC | 5336 |
| rs568444730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817452 | GCGCACGCTGGAGTG[C/T]ATCGTCTTGAGGGGT | 5336 |
| rs568458003 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892366 | GATACAGGATGTTGC[A/G]CTGATGTTCCAGTAT | 5336 |
| rs568464488 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81794183 | GACCACAAACACAGC[C/G]TGGAAAAGGGCTGTT | 5336 |
| rs568478223 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81930824 | CAACATAGAAAATTA[C/T]GCACAATATGCTAAG | 5336 |
| rs568488027 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888696 | GGAATGAGATGCCAA[C/G]CCAGGTAAGTGACCT | 5336 |
| rs568498394 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782506 | CATAGTTGATAAAGC[A/G]TGGAACGCTGGAGAC | 5336 |
| rs568503231 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81812431 | GATTTGCATTTCTCT[A/T]ATGACCAGTGATGAT | 5336 |
| rs568505357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847696 | TTGCATCTTACTGAA[C/T]ATGGACAAACTTTTT | 5336 |
| rs568525303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898542 | TATTTTTATCATCGT[C/T]ACTTTATTTTCACAT | 5336 |
| rs568534616 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910086 | ACTAAGGCCCTGCAT[A/C]TGGTTTTGTTGTTGT | 5336 |
| rs568539286 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909593 | GAATAACTTTTAAAT[G/T]TTTTGTAGAGCTGGA | 5336 |
| rs568542956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840376 | CCAGATTGGCCTGGG[A/G]GGATAGTGTGAGGAT | 5336 |
| rs568543940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847469 | ACCCTCTAATCACAT[C/T]GTTGGTTCCCCTGGC | 5336 |
| rs568563519 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877462 | TCCGTCTCAAACAAA[C/G]AAAACAACAAAACAC | 5336 |
| rs568566532 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81918737 | GCTATTTGGGGTAGA[C/G]ATTTTTAAAAAGACC | 5336 |
| rs568568922 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938712 | GCATTGAACTCATCC[A/C]GTGTCACTCTAGAAC | 5336 |
| rs568577033 | in-del | -/T | 0.303938 | 0.244112 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941703 | ACTGTAAACTCCCCC[-/T]TTTTTTTTTTTTGAG | 5336 |
| rs568615905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913210 | TCCCACTTCCACTAA[C/T]GACAAGGAGCCGAGG | 5336 |
| rs568625139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836712 | GCCACTGCACTCCAA[C/T]CTCAGCAACAGAGCA | 5336 |
| rs568632887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917164 | GTTTTTCTGTGCCTG[A/G]TTTATTTCACACAGC | 5336 |
| rs568637755 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81828533 | GTGAGCCACCGCACC[C/T]GGCCGAGAAGCGTCA | 5336 |
| rs568674396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815718 | CTTCTTCGATTCTCG[C/T]GGTCTTCTTGGTGGA | 5336 |
| rs568674498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840565 | ACAGTGACAGATCAT[C/G]AGGCATTAGATTCTC | 5336 |
| rs568677472 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961370 | CCTCTTTATCTCATT[A/C]AGTGATACATTTCCA | 5336 |
| rs568677532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803228 | GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCT | 5336 |
| rs568698944 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866813 | CCCCACGACCCCTCT[C/T]GCTGCCGCTCTGGTA | 5336 |
| rs568713405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806019 | TTATTAATAAATTTT[A/G]TTTAACTCAGTATAT | 5336 |
| rs568714860 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941617 | ATGAACATTGCTACT[C/G]TAGCAATAATAATGA | 5336 |
| rs568715634 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791783 | TTGGCCAGGCTGGTC[A/T]TGAGCTCCTGACCTC | 5336 |
| rs568721836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862562 | GCTTTTCCTTTTTTC[A/T]TTTTTCTTTTTTTAA | 5336 |
| rs568724894 | snp | A/G | 1.65795e-05 | 0.00287914 | missense | PLCG2 | GRCh38.p7 | 16:81936243 | AGACAGAAGCCCGTC[A/G]ACCTCCTGAAGTACA | 5336 |
| rs568725183 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926375 | GGCAGGTTGAAGGAG[G/T]GCGTTTGCATGTCTG | 5336 |
| rs568735915 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778231 | AGAGAAAATTAGCCA[A/G]GTGTGGTGTGCCTCT | 5336 |
| rs568776655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791488 | TTGGTGTCACCTCGC[A/C]TGGAAGGTTCCAGAA | 5336 |
| rs568786681 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802205 | GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC | 5336 |
| rs568787242 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916386 | AATGCCTTTTCTTGA[-/T]TTTTTTCCCTGCCAT | 5336 |
| rs568789641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810165 | CCCAGCTAATTTTGT[A/G]TTTTTAGTAGAGATG | 5336 |
| rs568804182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836078 | TGCAGTTCAACCCCC[A/G]ACATTACCCGTTTAT | 5336 |
| rs568815701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913827 | GGCTGCCCCCTGGGC[A/G]TTTGGATTTCCCTTC | 5336 |
| rs568818280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836292 | GTAGTGGCAGTGGGA[C/G]TGGATCGTGGATCTC | 5336 |
| rs568818720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862092 | ACTTTGACCAAGATG[C/T]CAATGAAAGAGCAAC | 5336 |
| rs568821743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883101 | CTTGTAGGTGAGGGA[C/T]ATTGTGTCACTCACC | 5336 |
| rs568825577 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803210 | TGCAAGCTCTGCCTC[A/G]TGGGTTCATGCCATT | 5336 |
| rs568835791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782807 | TGGTAAGGGCCCCTC[C/T]AACAGTTGAATGGAC | 5336 |
| rs568848068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858474 | TGGTTTTTTGAGGCT[C/T]GTTGAGTGTCTTGTA | 5336 |
| rs568848345 | snp | C/T | 6.64319e-05 | 0.00576295 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854615 | TTCTGTGCCTTTCTC[C/T]TTCCCTGTGCCTTAG | 5336 |
| rs568860753 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862390 | GCACTTTACATCCTT[A/G]GGATATGCTCTTGGC | 5336 |
| rs568873414 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778582 | CCCATGAGATCAGGA[A/G]AACGGGACATCAATT | 5336 |
| rs568873546 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866847 | CCTGTTCCCACTGCT[C/T]CTCCACCTTCATCCT | 5336 |
| rs568882388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938206 | GGCCGGAAAGAGAAA[C/G]AAAACATGGGAAACA | 5336 |
| rs568887392 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81865157 | CCTGAATTGAGACTA[G/T]AGGGCCAGGCCTTTG | 5336 |
| rs568888799 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871114 | GGCAAAATTCTTTAA[A/C]CATGACAGAGCTGTG | 5336 |
| rs568911865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882884 | TTGGGGCCTTCTCAG[A/C]CATTCCCACTCTTCC | 5336 |
| rs568928100 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81935541 | TTTCATCTTAGAACA[G/T]AAGACCAGCCAGACA | 5336 |
| rs568929557 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962055 | GTCCCTCCCGAAGCT[A/G]CGCGCTCCGTCGAAG | 5336 |
| rs568930487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847826 | GGATGTGCATAGGCT[A/G]TATGCAAATTCTCTG | 5336 |
| rs568943594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791035 | AAATAGGGTTTTGCT[C/G]TGAACCCTGTTTGGA | 5336 |
| rs568944451 | snp | A/G | 3.39213e-05 | 0.00411819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937942 | CCAGGGGAGCCAGCC[A/G]CCCTCCCTGGGGGCT | 5336 |
| rs568951367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942991 | GCGAGAGAAGGTACA[C/T]AGAGCTGGAGACAGC | 5336 |
| rs568965030 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81789604 | TCAATTCATTCTTTT[A/G]TTTATCTGTTCAGCC | 5336 |
| rs568967056 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81804284 | TTGTGGTTCTGATTT[G/T]CATTTTCCTGATTGC | 5336 |
| rs569000902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803275 | AGGTGCCCACCACCA[C/T]GCCTGTCTAATTTTT | 5336 |
| rs569012880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799776 | TTTTTTGTATTTTTA[G/T]TGGAGATGGGGTTTC | 5336 |
| rs569020328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812894 | AGTTTTCTGCATATG[A/G]CTAGCTGGTTTTCCC | 5336 |
| rs569036374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817276 | ATGCATCCATCCCCC[A/G]TGTATAAAATGGGAA | 5336 |
| rs569046951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894415 | GCCTGGGCAACAGAG[A/C]GAGACTCTGTGTCTA | 5336 |
| rs569048916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898985 | AATTCAGGAGTTTGA[A/G]ACCAGCAGCCTGGCC | 5336 |
| rs569056087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930116 | TGAGGTGGGTGGATC[C/T]CTTGAGCCCCAAGAG | 5336 |
| rs569062358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950745 | ATAATTTTCTAAATA[C/T]ACTAAAACAAGTAAA | 5336 |
| rs569068081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829068 | CTGTCTTTTTTGTAT[C/G]TGTGATTTTCATTCA | 5336 |
| rs569072072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825189 | AGCCACTAGGTTTGT[A/G]GGGCCATCCTGGCCT | 5336 |
| rs569108225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935520 | GTTTTGAGCTGCTTC[C/T]ATATCTTTCATCTTA | 5336 |
| rs569120177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914250 | GACAGCTCTGACACA[A/T]CCGGATCGGGGCCTC | 5336 |
| rs569120337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935144 | CAGAGTCTGAAATCA[G/T]TATCATGAGGTCAAC | 5336 |
| rs569125928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806392 | TGTGGAAGTGTGTCT[A/G]CCAGCTTTGCCATCT | 5336 |
| rs569130613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810847 | GTTTAGTGGGAGAGG[C/G]AAGCACAACATTGAT | 5336 |
| rs569147401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883811 | AACAGGTGATGCCTG[C/G]GACAGTCTCCCTGGA | 5336 |
| rs569159967 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81843421 | ACTGGAGAGGAACAT[C/T]TTTGGATTGCAATAT | 5336 |
| rs569178677 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959026 | CATGACAGTATGTGC[A/G]GCTGGCCAGGGCTTT | 5336 |
| rs569181757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939181 | CTAGGTTGGTCCTCT[C/T]TGTGCAACAGCCCAA | 5336 |
| rs569191481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814540 | TCTACTAAAACAATA[C/T]GAAAATTAGCCAGGC | 5336 |
| rs569194419 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828405 | ACCACGCCCGGCTAA[G/T]TTTTTTGTATTTTTA | 5336 |
| rs569198641 | in-del | -/A | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81844420 | CCCCACAATGGGTTC[-/A]AAGTGATTCTCCTGC | 5336 |
| rs569201734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918994 | TGGCAAACATTTTCT[C/G]TGAAGGACCACAGAG | 5336 |
| rs569235985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830870 | CAAGTGCAGAGACAG[C/T]GTGACTAGAATGTCC | 5336 |
| rs569244176 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844045 | GCAGTGGTGTGACGT[C/G]GGCTCACTACAAGCT | 5336 |
| rs569247409 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81909215 | AAAAGCAGTCACTCA[A/G]ATGATTTGCAAGTAT | 5336 |
| rs569249002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819284 | AGTCAGGACATCCTG[A/G]GGGTGTTGGATTCCC | 5336 |
| rs569254909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795582 | GTGTTGGAGGCTACC[A/G]CAGGATCCTTTGTGT | 5336 |
| rs569257897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867602 | GAACAACACCTGTCA[A/C]CTGATAAGCACTATT | 5336 |
| rs569258050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814080 | GATATTAGAAGGCTG[A/C]CCTCCATAAGGAGAG | 5336 |
| rs569285846 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81806070 | CATGTATGCAATATA[A/G]TTATTAACGAGATAT | 5336 |
| rs569304169 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884049 | CAGCCCCCCCTACCC[C/G]CCAGCGAAGAAGTAT | 5336 |
| rs569318377 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959703 | TCAAGAAAGGCTAGG[C/T]GAGAAAGGCACTGGG | 5336 |
| rs569319259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844623 | CACTGTGCCTGGCCC[A/G]CACCTTCACTGTTTT | 5336 |