| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs8357 | snp | C/G | 0.104504 | 0.2033 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958259 | TTGGCCTCTCATGTT[C/G]CAAACCTCATTGAAT | 5336 |
| rs1071644 | snp | C/T | 0.49473 | 0.051063 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81937798 | ATTGTTTTCTCTCAA[C/T]GGGCGCACGGGCTAC | 5336 |
| rs1130733 | snp | A/G | 0 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81938886 | GTGGAGCCGAGTATG[A/G]CAACAACAAGTTCAA | 5336 |
| rs1130756 | snp | C/T | 0 | 0 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958108 | TCTGTGACATCTTTT[C/T]TTCAAGCCTGCCATC | 5336 |
| rs1137750 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935169 | GTCAACATCAGGGTG[C/T]CAGCAGGGCTGTGCT | 5336 |
| rs1143685 | snp | C/T | 0.398955 | 0.200779 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81786163 | CTGGAGCAAGACCGC[C/T]GACAAGATCGAGGGC | 5336 |
| rs1143686 | snp | A/G | 0.39898 | 0.200773 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81854547 | CTGCTTCACCATCCT[A/G]TATGGCACTCAGTTC | 5336 |
| rs1143687 | snp | C/T | 0.118966 | 0.212909 | missense | PLCG2 | GRCh38.p7 | 16:81889208 | AACAAAGTCCGTGAG[C/T]GGATGACAAAGTTCA | 5336 |
| rs1143688 | snp | C/T | 0.48582 | 0.0830003 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895883 | CAAGATCAAGTTTGA[C/T]GACGTCGTGCAGGCC | 5336 |
| rs1143689 | snp | C/T | 0.339015 | 0.233625 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81907714 | CTACTGCGCCATTGC[C/T]GATGCCAAGCTGTCC | 5336 |
| rs1143690 | snp | C/T | 0.0198289 | 0.097577 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81936242 | CAGACAGAAGCCCGT[C/T]GACCTCCTGAAGTAC | 5336 |
| rs2965754 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933609 | TTGAGTagcctgggc[A/G]acagagtgagactct | 5336 |
| rs2966242 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81933576 | ctcaaaaaaaaaaaa[A/C]aaaaaaCAGCATGAC | 5336 |
| rs3088217 | snp | C/G | 0.499933 | 0.00579035 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962346 | TGTATAATTCCAAAT[C/G]TAATTATTAACTTTT | 5336 |
| rs3189935 | snp | C/G | 0 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81931553 | ATCCTGGAGCCCAAG[C/G]AGCAGGGCGATCCTC | 5336 |
| rs3813009 | snp | C/G | 0.168135 | 0.236216 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927353 | GATTGAGTTGTTGTG[C/G]GTGAGTTGCTGTGAC | 5336 |
| rs3813010 | snp | C/T | 0.426354 | 0.177198 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927397 | TTTAATCAGGTTGTG[C/T]TGGGCTTGGAAGGAT | 5336 |
| rs3813011 | snp | A/G | 0.286303 | 0.24735 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932957 | CTCTGAGGCACAGGG[A/G]GGTGCCACGACCCTG | 5336 |
| rs3893311 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867962 | cctgtaatcccagca[C/T]tttgggaggctgagg | 5336 |
| rs3922849 | snp | C/T | 0.49941 | 0.0171624 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921572 | TTTTTGGCTCGCTGA[C/T]AGAGCCTGTGGTGTT | 5336 |
| rs3922850 | snp | A/G | 0.451608 | 0.147832 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921633 | TGCAGTGCAAATGCT[A/G]TCTCATATTCCCACC | 5336 |
| rs3923153 | snp | C/T | 0.304438 | 0.244001 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930399 | CTCATGGCTGCATTC[C/T]TCAGTCTCCACATTT | 5336 |
| rs3924349 | snp | G/T | 0.408188 | 0.193589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795876 | GGCCCCCTCCCACCT[G/T]CTATTGAACAGAATT | 5336 |
| rs3934954 | snp | A/G | 0.41325 | 0.18934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936754 | CATTTACATGCTGGC[A/G]TAACTAACATACACA | 5336 |
| rs3934955 | snp | A/C | 0.498253 | 0.0295011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936761 | ATGCTGGCATAACTA[A/C]CATACACAAACTTCT | 5336 |
| rs3934956 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936802 | TGATCGCATAAATCA[C/T]GGGGCTTTGTGCTTT | 5336 |
| rs3934957 | snp | C/G | 0.49706 | 0.0382258 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936866 | CTATTCATCAGTAGC[C/G]TCCTTTACATTCTTT | 5336 |
| rs3934985 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867728 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCCAA | 5336 |
| rs3934986 | snp | G/T | 0.130008 | 0.219321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867991 | GCAAGggccaggcac[G/T]gtggtggctcacgcc | 5336 |
| rs3935625 | snp | A/C/G | 6.73991e-05 | 0.00580474 | missense | PLCG2 | GRCh38.p7 | 16:81905422 | ACATCCACATCGCCT[A/C/G]GGGGGCCCAGCTTCT | 5336 |
| rs3935647 | snp | C/T | 0.488241 | 0.0757703 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81779166 | GGAGCGCACCCCGAG[C/T]GCAGCGTCCCCGCGC | 5336 |
| rs3935743 | snp | A/C | 0.25801 | 0.249872 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876375 | GTACTTAGGCTGTAG[A/C]AACCATTTGGTTCTG | 5336 |
| rs3935744 | snp | C/T | 0.330947 | 0.236533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876232 | AGTTCAAGCCTAGCC[C/T]GGGTAACATGGTGAA | 5336 |
| rs3935876 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867190 | GGCTGGGCAGTGACG[C/T]GCTACTTCCTTCCGC | 5336 |
| rs3935877 | snp | C/T | 0.276267 | 0.248616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867248 | TACAGGGAAACTAGG[C/T]GGTTTTCTCCTGCAA | 5336 |
| rs3936112 | snp | A/G | 0.358728 | 0.225118 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937333 | CACTGCTCCCTAAAT[A/G]AGGGAAAAACTGGTT | 5336 |
| rs4072681 | snp | G/T | 0.49089 | 0.0668743 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853886 | ATCCAGAACCCCTGT[G/T]ACCATCCCCAACGCT | 5336 |
| rs4072682 | snp | C/T | 0.405255 | 0.195948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853898 | TGTTACCATCCCCAA[C/T]GCTGGGGTTGGCCTC | 5336 |
| rs4072683 | snp | C/T | 0.314057 | 0.241654 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853936 | TATTTTTAATTTGAA[C/T]CAGTTAGTGCCTTCA | 5336 |
| rs4072828 | snp | C/G | 0.398657 | 0.201013 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854632 | ACTTCTTCAGGAAGA[C/G]ACTAAGGCACAGGGA | 5336 |
| rs4072830 | snp | G/T | 0.362523 | 0.223246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854352 | CAGGCACAGCCTGGC[G/T]CCTTCCTTCCCCAAC | 5336 |
| rs4072831 | snp | C/T | 0.334182 | 0.235401 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854298 | CGTCTGGACTCAGTG[C/T]CCCCTCCTTCTGGAA | 5336 |
| rs4073295 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836417 | GGATCTTGGCTTCTC[A/G]TTTCATCCTTCCCTT | 5336 |
| rs4073313 | snp | C/G | 0.178465 | 0.239547 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780108 | ATTAGGGTACCAAGA[C/G]AGCCCCGCCCCACCG | 5336 |
| rs4073314 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81780583 | TCATTAGGTGACTTA[A/C]ACATCAGTGAGGCTC | 5336 |
| rs4073828 | snp | A/G | 0.496999 | 0.0386216 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936890 | ATTCTTTTTATAGCC[A/G]CATCGGATTCCACAG | 5336 |
| rs4073829 | snp | C/G | 0.388587 | 0.208071 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936583 | AGGCTGCTTGGCTTA[C/G]GCAGGCTTCGTGATT | 5336 |
| rs4074445 | snp | G/T | 0.108048 | 0.20579 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856277 | aacacctcatggAAC[G/T]ATGAAGCCTCTCCTT | 5336 |
| rs4076360 | snp | C/T | 0.464523 | 0.128375 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893289 | CAGGCACAGAACAGA[C/T]ATTCAACAACTGTTG | 5336 |
| rs4077748 | snp | C/G | 0.10237 | 0.201756 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814624 | cactgcaacctccac[C/G]tcccgggttcaagtg | 5336 |
| rs4077797 | snp | C/T | 0.367708 | 0.220556 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865664 | GGGGCCCTGGCCTCT[C/T]CCTTGCTCCCAGGAT | 5336 |
| rs4077853 | snp | C/T | 0.463126 | 0.13068 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937365 | GAAGCACAAATAGTT[C/T]CCAGAAAAGAAAATG | 5336 |
| rs4078270 | snp | A/C | 0.223225 | 0.248562 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942075 | AGAAATCTGTTACAG[A/C]GTCAAGGCTAGGAAC | 5336 |
| rs4133124 | snp | A/C | 0.493703 | 0.0557558 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885924 | CTCAAACTTAGTCTC[A/C]GGTTGGGCAAATAAG | 5336 |
| rs4133125 | snp | G/T | 0.25045 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885861 | ACTAGGAAGGCATGA[G/T]GATTACAACACGCAT | 5336 |
| rs4243210 | snp | C/T | 0.308661 | 0.24302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785343 | CAGTCTACCCAGAGC[C/T]ACACAGTCAGCAGGA | 5336 |
| rs4243211 | snp | A/G | 0.469049 | 0.120489 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786911 | TCCCTAAACCATCCT[A/G]CTGAGGCAAGCTCAT | 5336 |
| rs4243212 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815668 | AGCATGGGAAAATCC[A/T]GCCTGATTTTTTCCA | 5336 |
| rs4243213 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815712 | TGGTGGCTTCTTCGA[C/T]TCTCGCGGTCTTCTT | 5336 |
| rs4243214 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815770 | CGCTATAATTGAGCA[C/G]TCTTAAATgaccaga | 5336 |
| rs4243215 | snp | A/G | 0.227369 | 0.248974 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815777 | ATTGAGCAGTCTTAA[A/G]Tgaccagacacagtg | 5336 |
| rs4243216 | snp | A/G | 0.41023 | 0.191902 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817172 | GGACAGGAAGAGCGC[A/G]CATGATGGGTGGTCA | 5336 |
| rs4243217 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817189 | ATGATGGGTGGTCAG[A/G]AAAGGCCTCTCTGAG | 5336 |
| rs4243218 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867023 | TCTGTCTGTGAAAGC[C/T]GTGGGTGCTGTCCCT | 5336 |
| rs4243219 | snp | C/G | 0.425432 | 0.178112 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875784 | AAGAAAATTGAGAAG[C/G]CTGCTAACGTATCTC | 5336 |
| rs4243220 | snp | A/G | 0.273856 | 0.248859 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903173 | gcaGTAGGCAGAGAA[A/G]GGGGATGTCCTTCCA | 5336 |
| rs4243222 | snp | C/T | 0.499974 | 0.00359416 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912818 | GCTCACCTGCAGTGC[C/T]CTGCCCCCCCAGCAT | 5336 |
| rs4243223 | snp | G/T | 0.499968 | 0.00399348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912866 | ACCACAGCAAAAGCC[G/T]CTGCGAGAATGTGCG | 5336 |
| rs4243224 | snp | G/T | 0.424193 | 0.179323 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927986 | GTGCAGGGGGTGGGG[G/T]TTGGGGTGGTGCAGG | 5336 |
| rs4243225 | snp | G/T | 0.253264 | 0.249979 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948043 | CCCTAATTCACTTAT[G/T]CTCCTACTAACGGAG | 5336 |
| rs4243226 | snp | A/G | 0.335101 | 0.23507 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960369 | ACTAGTAACAGGCAC[A/G]TTCTGAAAGATGGAA | 5336 |
| rs4254322 | snp | A/G | 0.304188 | 0.244057 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779948 | GATGCCCGCTCCGCA[A/G]CTGTCTGCGTAATTA | 5336 |
| rs4258606 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795956 | TGCTAGAAGAACAGG[A/G]CCTAAGTTGGGGGGC | 5336 |
| rs4258607 | snp | C/T | 0.428635 | 0.174898 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833805 | CTCCTGCCTTGGCCT[C/T]CCAAAGTGGTGGGGT | 5336 |
| rs4258608 | snp | A/G | 0.466204 | 0.125522 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937977 | CGATGCTGTCTTGAG[A/G]GCAGGGAACCCATGT | 5336 |
| rs4264387 | snp | C/T | 0.341909 | 0.232492 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905632 | CAAGTGAGTTTTTGC[C/T]ATGTGAATTTACCTT | 5336 |
| rs4265800 | snp | A/T | 0.397994 | 0.201489 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798627 | TACAAGTTGTGCTGG[A/T]GGCCAGGGGTAGGCG | 5336 |
| rs4273032 | snp | A/G | 0.40157 | 0.198813 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778631 | CTGACTCCCTTTGGG[A/G]CTGGCACTATGTTGA | 5336 |
| rs4274427 | snp | A/C | 0.257732 | 0.24988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787666 | TGCAAGCACCACTCC[A/C]ATCAAAAGTAGAACC | 5336 |
| rs4274430 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799994 | GACTGCCTGGGTTCA[A/G]ATCTTGGCTATGCCA | 5336 |
| rs4281703 | snp | C/G | 0.377977 | 0.21476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784835 | GTCCCTGGTGGTTCA[C/G]CTCCAGGGCCTGGGG | 5336 |
| rs4281704 | snp | C/G | 0.342806 | 0.232136 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784854 | CAGGGCCTGGGGAGC[C/G]CCTTCACTCTAAGTC | 5336 |
| rs4281705 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784918 | TTTGGGAGGCAGAAT[A/G]AGGGAATGGTACAGA | 5336 |
| rs4284633 | snp | A/G | 0.140242 | 0.224618 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947135 | ACAACCGGAAACATT[A/G]TAAATAATTTAAGTG | 5336 |
| rs4286102 | snp | C/T | 0.272511 | 0.248984 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904358 | aaatctggatctgac[C/T]ccctatcctgagctc | 5336 |
| rs4286103 | snp | C/T | 0.435694 | 0.167385 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959301 | CCTCCTCTTGTTACC[C/T]GAAATGCTGGGCTTA | 5336 |
| rs4288988 | snp | G/T | 0.27008 | 0.249192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787677 | ctccaatcaaaagta[G/T]aacctttatatcacc | 5336 |
| rs4293371 | snp | C/G | 0.227664 | 0.249 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793248 | AGGAGCTGGTTGTCT[C/G]TGAATGTCGGGAGGG | 5336 |
| rs4294811 | snp | A/G | 0.404815 | 0.196297 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786215 | GGGGCAGTGTGGCCC[A/G]TCCTCTGGGGCCCTG | 5336 |
| rs4305012 | snp | A/G | 0.232067 | 0.249356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904109 | TTTGCTGAGGAAATT[A/G]TTCAAGGCCAAGGTG | 5336 |
| rs4306503 | snp | C/T | 0.123798 | 0.215808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905861 | gatgggatttagtcg[C/T]gttgcccagggtgat | 5336 |
| rs4306504 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913109 | AGGCCTGTGATGATA[C/T]AGATCTGGTTTCCTC | 5336 |
| rs4312298 | snp | G/T | 0.466308 | 0.125343 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947571 | GGTAAACAGCCTCAA[G/T]GCAGACTTTTCTGAG | 5336 |
| rs4312300 | snp | C/G | 0.489259 | 0.0724914 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778495 | AAAGAGCATAGGAAG[C/G]GTTTGAATCAGATAG | 5336 |
| rs4313806 | snp | A/C | 0.498253 | 0.0295011 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916622 | AAAGTCTACCCTCAG[A/C]AATTTTCAAGAATAC | 5336 |
| rs4319763 | snp | C/G | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779792 | GCCGTCTCTCTTGAC[C/G]GCCCTTGTGCCCAGA | 5336 |
| rs4322655 | snp | C/G | 0.385932 | 0.209815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822938 | AAGCAGGTTTTCCCT[C/G]GGAGCCTCCAGAAGG | 5336 |
| rs4322656 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813579 | ttTCTATAACAGTGT[A/G]aaaacacaggagctt | 5336 |
| rs4325546 | snp | C/T | 0.468949 | 0.12067 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840216 | GCTGCCTGGAGAGCA[C/T]GCTTAGAATTGAGCC | 5336 |
| rs4334287 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867750 | TCACCCAGGCTGGAG[G/T]GCAGTGGCGTGATCT | 5336 |
| rs4335765 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917866 | agctgggactacagg[C/T]gcccgccactgcgcc | 5336 |
| rs4337289 | snp | C/G | 0.498437 | 0.0279115 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931123 | TTTTTTTTCCTGCAT[C/G]TTAAGTGTCCCTCTC | 5336 |
| rs4338799 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783470 | AACCTCTTTTGAGAG[G/T]GGCAAGTACTGGCAA | 5336 |
| rs4341734 | snp | C/G | 0.331411 | 0.236373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858393 | ATTTGCGTAGTTGCT[C/G]ATTCCTTTATTCTGC | 5336 |
| rs4341735 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922681 | AGGAAAAATTTTACT[A/G]GGTTCCCTGTGAAAT | 5336 |
| rs4354929 | snp | C/G | 0.496999 | 0.0386216 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785881 | TTCCTGAAGTTCATG[C/G]CCTGTTAACTAAACC | 5336 |
| rs4366702 | snp | A/C | 0.429747 | 0.177031 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928466 | AACAGTTCCACAGGC[A/C]GTATCTCTGCTAAAC | 5336 |
| rs4369658 | snp | C/T | 0.498632 | 0.0261223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909788 | gtgctgggcagtatt[C/T]gagacaccttgtgtg | 5336 |
| rs4369659 | snp | A/G | 0.490398 | 0.0686206 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938072 | CTTACAGTACACTCC[A/G]GGGTCGTTCTGGGAG | 5336 |
| rs4375654 | snp | C/G | 0.340784 | 0.232934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905859 | gagatgggatttagt[C/G]gtgttgcccagggtg | 5336 |
| rs4386130 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823578 | TCGCCCAGGCTGGAG[G/T]GCAGTAGTGTGATCA | 5336 |
| rs4387596 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813990 | CCAGAGATGGAGACC[A/C]TGGTATTCAGGGGCA | 5336 |
| rs4392063 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818166 | TTAAGCTCTTACTCC[C/T]GTTAGGATTGCTTCG | 5336 |
| rs4392065 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905802 | gtctctgggaccaca[C/T]gtgcgcaccaccatg | 5336 |
| rs4395069 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942326 | TTAGCTTGGAGATTT[A/G]GAAAAAACAAAGGTC | 5336 |
| rs4396528 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813742 | gcagctttctgggcc[A/G]ccagtgttcctttgt | 5336 |
| rs4398100 | snp | C/T | 0.210909 | 0.246925 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780739 | AAACTTTTGAAAACA[C/T]TTCTTGGTCAGGCAC | 5336 |
| rs4398101 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817558 | CAAGTGATAAAACAA[C/G]AGCCCTCAAACTGCA | 5336 |
| rs4399527 | snp | C/G | 0.496517 | 0.0415876 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827718 | GTGGACAGATCCTAC[C/G]TCATGCTGCAGGCTC | 5336 |
| rs4401042 | snp | A/G | 0.489083 | 0.0730708 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778787 | CAATTCCTGGCGGGT[A/G]ATTGTGAAGAGTATA | 5336 |
| rs4404063 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81814824 | AACCTCTCTGAACCT[C/T]AGTTTCTTTGTCTCT | 5336 |
| rs4405545 | snp | A/G | 0.345482 | 0.231048 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824567 | TTGGATCTCCCTCAG[A/G]CCTTCTCACCATGTT | 5336 |
| rs4405546 | snp | A/C | 0.130973 | 0.219847 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939869 | TCCAATGTGGCCTCT[A/C]ATGAGCTTTGATCTC | 5336 |
| rs4410068 | snp | A/G | 0.210909 | 0.246925 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780448 | GGGCCCTCGTCCTTG[A/G]CTACAGTTCTGCGGG | 5336 |
| rs4410069 | snp | A/C | 0.431769 | 0.17164 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887701 | ACACACACATCTGGT[A/C]GCATATTTGCTTCTA | 5336 |
| rs4414487 | snp | C/T | 0.178785 | 0.239642 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888204 | TTGCACAAGCTGCCA[C/T]GGTCAGAGTACtttc | 5336 |
| rs4417543 | snp | A/G | 0.488726 | 0.0742286 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822488 | ggggctgggggcagt[A/G]gctcatgcctgtaat | 5336 |
| rs4420523 | snp | A/C | 0.482083 | 0.0929373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893175 | CGGAACACAAATTTT[A/C]AAAAAGTTGGGGTGA | 5336 |
| rs4423414 | snp | C/G | 0.111224 | 0.207945 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880016 | GGGCTCAGGAGGGAG[C/G]ATCTCTTGAGGCCAG | 5336 |
| rs4424903 | snp | A/G | 0.175576 | 0.238665 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903960 | TGCACTTGGCTAGGC[A/G]TGGTCATATGTATCT | 5336 |
| rs4426345 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890494 | CATAGCCCTTTCTTA[C/T]TCTTCTCTACTGACC | 5336 |
| rs4426346 | snp | A/T | 0.496314 | 0.0427728 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922672 | TGTGTTCTGAGGAAA[A/T]ATTTTACTAGGTTCC | 5336 |
| rs4429291 | snp | A/G | 0.0123155 | 0.0776139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819149 | TGTGGGGTTCAGTGG[A/G]GGTTGGCGGTGCTTG | 5336 |
| rs4429292 | snp | A/T | 0.437824 | 0.164991 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819386 | CCTGTGAGGCGAGGG[A/T]GCTCCTGCGAATCCC | 5336 |
| rs4435247 | snp | C/T | 0.110167 | 0.207236 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879922 | GATATTTCTTTCGTC[C/T]TCTTGCCTTCGAAGA | 5336 |
| rs4435248 | snp | C/G | 0.291705 | 0.246497 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905545 | AGCCACTGCGGCCAC[C/G]CCCCTTGCAGCTGCT | 5336 |
| rs4439757 | snp | A/T | 0.323434 | 0.238972 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905072 | tttttatttttgtag[A/T]tacagggttttgcca | 5336 |
| rs4448931 | snp | A/T | 0.471483 | 0.115954 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893006 | CGAGCCACCATGCCC[A/T]GTTTTGTTTTGTTTT | 5336 |
| rs4450393 | snp | G/T | 0.498323 | 0.0289051 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916695 | cagtctggagtgcag[G/T]ggcgtgatcttggct | 5336 |
| rs4456499 | snp | A/G | 0.20511 | 0.245937 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817311 | ATTAGTACCTGTGCC[A/G]TGAGGCAGTTGTGAA | 5336 |
| rs4468612 | snp | A/G | 0.461259 | 0.133677 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827951 | CAAAAGTAGCCAGGC[A/G]TGGTGGCGGATGCCT | 5336 |
| rs4471676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783731 | ACAAGGATGAAATGG[A/G]CCATGGGGGCACCTT | 5336 |
| rs4476171 | snp | A/T | 0.00398731 | 0.0445001 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783182 | TATGTTCCAGTGGAC[A/T]ATGGCCTAGAGACCT | 5336 |
| rs4476173 | snp | C/T | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81779787 | GTGGCGCCGTCTCTC[C/T]TGACGGCCCTTGTGC | 5336 |
| rs4476174 | snp | A/G | 0.491157 | 0.065903 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784923 | GAGGCAGAATGAGGG[A/G]ATGGTACAGAGTGAG | 5336 |
| rs4480797 | snp | A/C | 0.490618 | 0.0678448 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785224 | GCATAAACAGCAATC[A/C]AGGACACCTCCTAGG | 5336 |
| rs4480798 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947530 | TTATTTATCACCATA[G/T]CCTCTGGAAGCCAGG | 5336 |
| rs4482276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904362 | ctggatctgaccccc[C/T]atcctgagctccttc | 5336 |
| rs4485360 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923322 | GCTTTTTGGGGCCTT[C/G]GATCCTTTGCAATGC | 5336 |
| rs4485361 | snp | C/T | 0.00324949 | 0.0401769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923622 | GGAGGCTGGGCTGCT[C/T]GGCAGGTGGGCTTGA | 5336 |
| rs4485362 | snp | G/T | 0.409041 | 0.192888 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942226 | ACCCCTCCCAGTGCC[G/T]TGCAGAGATGTCAGA | 5336 |
| rs4485363 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942374 | TAAAAATGTGACCTT[C/G]TCCTCCCCCGACTGT | 5336 |
| rs4488437 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787117 | atgacatgtaatggc[A/G]caggcctcaatgtaa | 5336 |
| rs4494532 | snp | A/C | 0.311123 | 0.242413 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903852 | CCCCTTTTAGAGCAC[A/C]CTCTGCCCCACACCT | 5336 |
| rs4494534 | snp | A/G | 0.488666 | 0.0744214 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778405 | CTCAAGCAACTTGGA[A/G]GTGAAATTCAAGTGC | 5336 |
| rs4494535 | snp | A/G | 0.489201 | 0.0726845 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778447 | CTAGGTGCCCCTGAA[A/G]CTGCCTCTAGTCACA | 5336 |
| rs4496135 | snp | A/G | 0.489142 | 0.0728777 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778802 | AATTGTGAAGAGTAT[A/G]TTTATTTTTAATTTT | 5336 |
| rs4497678 | snp | C/G | 0.401215 | 0.199083 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850908 | AGATTTAAGATGGGG[C/G]CCGCTTATTTTTGTT | 5336 |
| rs4499225 | snp | A/G | 0.359364 | 0.22481 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865606 | TCTCTCTGTTCCTGG[A/G]CATGGGATGGTTCCT | 5336 |
| rs4500720 | snp | C/T | 0.489259 | 0.0724914 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778670 | TACAGATGGGGAAAC[C/T]GAGGCTGTCGGTTTT | 5336 |
| rs4500721 | snp | A/G/T | 0.334412 | 0.235318 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837684 | TTGGTACCAACATGT[A/G/T]TTTTTTTTTTTTTTT | 5336 |
| rs4500722 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851145 | CCCTAATAATAGGGC[C/T]ACCCATAATTGAGAA | 5336 |
| rs4508413 | snp | A/C | 0.465263 | 0.127129 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944865 | CATAGATATCAAGGG[A/C]CAACTGTAGAGTAAA | 5336 |
| rs4508415 | snp | C/G | 0.469049 | 0.120489 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801504 | TCACTCAACAGTACA[C/G]CACGATAGATTGATC | 5336 |
| rs4510005 | snp | C/T | 0.347032 | 0.230401 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906396 | CTTATATCCTAGATA[C/T]AACATACATATCAAA | 5336 |
| rs4511521 | snp | C/T | 0.490782 | 0.0672626 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778947 | ATGACAGGCGTGAGC[C/T]CGGGCGCCCGGCCGG | 5336 |
| rs4511523 | snp | C/T | 0.250732 | 0.249999 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785405 | AAGACCTGACATTTC[C/T]TGCCTTTCATCCTCA | 5336 |
| rs4519328 | snp | A/T | 0.475789 | 0.107327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943713 | ATATCACTGGGCTAG[A/T]CTGCAAGAATTCTGA | 5336 |
| rs4520827 | snp | C/T | 0.158302 | 0.232576 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903969 | CTAGGCGTGGTCATA[C/T]GTATCTTCTTATTCA | 5336 |
| rs4520828 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943127 | GATAGCCTCCCGGAA[C/T]GCCATGGAGCAAACA | 5336 |
| rs4522412 | snp | C/T | 0.333722 | 0.235565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854333 | GATAGCTTTGCGGGA[C/T]CCTGTTGGGGAAGGA | 5336 |
| rs4530128 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817578 | CTCAAACTGCACCTG[C/G]CCTTCCAGAAGATGA | 5336 |
| rs4533279 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815434 | ACCCTGTCTTTCCAG[C/T]GGGAAACTGCAGGGG | 5336 |
| rs4534836 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813701 | cctgaatatattcat[C/T]ggatggccaggctgg | 5336 |
| rs4536469 | snp | C/T | 0.408871 | 0.193029 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944619 | acaggtgtgcatcac[C/T]gtgcccagctaaatt | 5336 |
| rs4538005 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81958498 | GAAGCCCTACCCACA[A/G]GCAGCCTGCTCAGTT | 5336 |
| rs4545811 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901004 | AGATAATACTGGAAC[C/T]CATCTGGCTAGCTTG | 5336 |
| rs4547325 | snp | C/T | 0.252702 | 0.249985 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831414 | TAAACACAGGCTGTG[C/T]GCCAGGCACTGCACT | 5336 |
| rs4548854 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81817504 | GTTTTAAACGCCTTT[C/T]GTCAGCTGTGTTTGG | 5336 |
| rs4552019 | snp | A/G | 0.155656 | 0.231515 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905799 | tgagtctctgggacc[A/G]cacgtgcgcaccacc | 5336 |
| rs4559900 | snp | G/T | 0.399073 | 0.200692 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820824 | cagggtctcatcatg[G/T]tggctaggctagtct | 5336 |
| rs4561462 | snp | C/G | 0.491263 | 0.0655142 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785234 | CAATCAAGGACACCT[C/G]CTAGGTGCTGGCCGT | 5336 |
| rs4563037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903371 | GAGCTTTGGCCAAGC[A/G]CAACCAGAGGAGGGG | 5336 |
| rs4569271 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PLCG2 | GRCh38.p7 | 16:81839809 | TAATCCCAACACTTG[C/G]GGAAACCAAAATGGG | 5336 |
| rs4577081 | snp | A/G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81893459 | ACACGTCCTCTCCAC[A/G/T]CTTGCATTGCCCAGG | 5336 |
| rs4577082 | snp | C/G | 0.490287 | 0.0690083 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784510 | CTCTCACTCCTCCTT[C/G]TTTGGATCCTGGGAG | 5336 |
| rs4580153 | snp | C/T | 0.340333 | 0.233109 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783634 | AGTTTTCCGCTGCCG[C/T]ATTTCCCATTGAGAT | 5336 |
| rs4580154 | snp | A/C | 0.490943 | 0.0666801 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785255 | TGCTGGCCGTCACCC[A/C]AGGTGCTTTGCTGGG | 5336 |
| rs4583233 | snp | A/C | 0.450609 | 0.149185 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786881 | GGGTTAAGGAGTCAA[A/C]TCAAATATTTCTCCT | 5336 |
| rs4584816 | snp | C/T | 0.242201 | 0.249878 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787598 | tatacatagaattca[C/T]ccattgtatgcagca | 5336 |
| rs4587966 | snp | C/T | 0.489318 | 0.0722982 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778479 | CAAAGATACCTCCAT[C/T]AAAGAGCATAGGAAG | 5336 |
| rs4587967 | snp | C/G | 0.301681 | 0.2446 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813850 | TGATGGCTTCCAAGG[C/G]ACAGAAAGCAGAAGC | 5336 |
| rs4587968 | snp | C/T | 0.340784 | 0.232934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905868 | tttagtcgtgttgcc[C/T]agggtgatttcaaac | 5336 |
| rs4591139 | snp | C/T | 0.451732 | 0.147663 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787103 | TCTTTCTTGGACACA[C/T]GACATGTAATGGCAC | 5336 |
| rs4595796 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801583 | CGATTCCAGCAAACA[C/T]GTCTTCGCTATTGTT | 5336 |
| rs4603554 | snp | C/T | 0.268452 | 0.249318 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948062 | CTACTAACGGAGAGT[C/T]AAGTCGTTGGCAGTT | 5336 |
| rs4606713 | snp | A/C/G | 0.00132216 | 0.0256777 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937945 | GGGGAGCCAGCCGCC[A/C/G]TCCCTGGGGGCTGGG | 5336 |
| rs4611451 | snp | C/T | 0.475613 | 0.107697 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938052 | GTGTTTGAGGATCTT[C/T]CTTTCTTACAGTACA | 5336 |
| rs4611452 | snp | A/G | 0.366473 | 0.221211 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943759 | AAAAACAAACTAGCA[A/G]CAAAAATCACATTGT | 5336 |
| rs4616280 | snp | C/T | 0.344147 | 0.231595 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831308 | ACAGTGCCTGGCACG[C/T]TGGCTTTTACCTACT | 5336 |
| rs4622505 | snp | C/T | 0.477515 | 0.103619 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904517 | acacagctggtagaa[C/T]agctgcagtgctgtt | 5336 |
| rs4627338 | snp | C/T | 0.130008 | 0.219321 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868004 | accgtgcctggccCT[C/T]GCTTCCCGCTTCAGC | 5336 |
| rs4627340 | snp | G/T | 0.159292 | 0.232964 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903951 | TTTGTACCATGCACT[G/T]GGCTAGGCGTGGTCA | 5336 |
| rs4628964 | snp | C/T | 0.170733 | 0.237101 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904762 | CCTGCCCTCATGGGG[C/T]TTATATTCTAGCAGT | 5336 |
| rs4640175 | snp | A/G | 0.438946 | 0.163706 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819385 | CCCTGTGAGGCGAGG[A/G]AGCTCCTGCGAATCC | 5336 |
| rs4640176 | snp | G/T | 0.149383 | 0.232019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943100 | CATGCTATTGGAGTG[G/T]AGGGGCTACCTGATA | 5336 |
| rs4888174 | snp | A/G | 0.211212 | 0.246973 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781457 | GCAACTATTGCTTCC[A/G]TGATTTTCTGTCGTA | 5336 |
| rs4888175 | snp | C/T | 0.461259 | 0.133677 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781533 | GGATCGAAGCATATG[C/T]GTGTTTTGCTTTTTA | 5336 |
| rs4888176 | snp | C/T | 0.238171 | 0.24972 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808607 | caagccattctcctg[C/T]ctcagcctcctgagt | 5336 |
| rs4888177 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81819692 | TGGTTTCAAGCGAAT[A/C]TCCTGCCTCAGCCTC | 5336 |
| rs4888179 | snp | A/G | 0.122064 | 0.214785 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850242 | TTTTGTTAGGTGTAA[A/G]GTTTTATGGTTCTAT | 5336 |
| rs4888180 | snp | C/G | 0.405255 | 0.195948 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857827 | GGACACATGACTGAA[C/G]CTGTCTTAGGTTCAG | 5336 |
| rs4888181 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858693 | ACTGATCAAAGGACA[A/G]ATACAGGGTCTGGAA | 5336 |
| rs4888182 | snp | A/T | 0.495483 | 0.0473088 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858893 | CATCAGAAGGAATTG[A/T]CAATGTAAAGAAACC | 5336 |
| rs4888183 | snp | A/T | 0.494811 | 0.050669 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859103 | CTTTCTTTTGTCTCA[A/T]ATTTCTTTCCAGTTG | 5336 |
| rs4888184 | snp | A/G | 0.281049 | 0.248064 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873876 | GGTAACATTCCACAT[A/G]AGAGGTATTTCAACC | 5336 |
| rs4888185 | snp | A/G | 0.150667 | 0.229419 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902431 | tgccgacttctagtt[A/G]tgtcctcacatggtg | 5336 |
| rs4888186 | snp | A/C | 0.127254 | 0.217792 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913551 | CTCCAGAGTCTCTAG[A/C]CAGAGGCCTGGGGGC | 5336 |
| rs4888187 | snp | C/T | 0.449218 | 0.151037 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918293 | CAATGCTACGGAGGT[C/T]TTCCTCTCTGTTTTC | 5336 |
| rs4888188 | snp | G/T | 0.497151 | 0.037632 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918332 | GTTTTACAGTTTCAG[G/T]TCTTATGTTTAAGTC | 5336 |
| rs4888189 | snp | G/T | 0.424659 | 0.17887 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927735 | TTATTTTCTAAGGGA[G/T]GTAGGGCAATCTGGG | 5336 |
| rs4888190 | snp | G/T | 0.398894 | 0.200825 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930013 | TGACTTTCCACATGT[G/T]ACTTTCTCTTAATGA | 5336 |
| rs4888191 | snp | A/G | 0.324619 | 0.238604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938365 | TGCATTTCTCCTAAG[A/G]TTAAGGGCGGGCGGG | 5336 |
| rs4888192 | snp | A/C | 0.475877 | 0.107142 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938684 | TCCAGTGAATCTAGG[A/C]AAATTAGGGCTGGCA | 5336 |
| rs4888194 | snp | C/G/T | 0.302493 | 0.244427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940459 | ACCTTTGGCATCTTG[C/G/T]GGGGGGAGTAACAAT | 5336 |
| rs4888195 | snp | A/G | 0.287867 | 0.247116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940481 | AGTAACAATCTCGAG[A/G]GTCCAACTCCCCAAA | 5336 |
| rs4888196 | snp | A/G | 0.279195 | 0.248289 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940658 | CAAGCTGGGTCATAC[A/G]ACCAGCTCTTAAGAA | 5336 |
| rs4888197 | snp | A/G | 0.233818 | 0.249476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950832 | GCCTTAAAACTTCAC[A/G]AAGAATGAAGACGTA | 5336 |
| rs4888198 | snp | A/G | 0.21875 | 0.248039 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955530 | TTTTTCTCCCCTAGC[A/G]TAATGGACTATTTTG | 5336 |
| rs4888199 | snp | C/G | 0.488057 | 0.0763479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955777 | GTTGGCCTTGCTTGG[C/G]TCATGTGCCTGGAGG | 5336 |
| rs4889381 | snp | C/T | 0.461037 | 0.134028 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781618 | TGCAGTGGCTGACAC[C/T]ATTCCTTTGAAAATA | 5336 |
| rs4889382 | snp | A/T | 0.446249 | 0.154875 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786718 | TCCCCTACCTCCGTT[A/T]GATTGGGCAGCTGGT | 5336 |
| rs4889383 | snp | C/T | 0.17138 | 0.237316 | intron-variant | PLCG2 | GRCh38.p7 | 16:81786978 | TGCATAATGTGTGGG[C/T]TTAAAAAGAAAACAA | 5336 |
| rs4889384 | snp | C/T | 0.403334 | 0.197456 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796870 | CTGTTGTTTCGGCCA[C/T]CCAATTTTTGGTATT | 5336 |
| rs4889385 | snp | C/T | 0.40157 | 0.198813 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798176 | GGTAATAGTGGAGCT[C/T]ACCCCATCAGATCAC | 5336 |
| rs4889386 | snp | A/T | 0.420574 | 0.182769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798269 | CCCAGCCATGCTGCC[A/T]TATGTCTCCTCAGGC | 5336 |
| rs4889387 | snp | A/G | 0.113685 | 0.209567 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805179 | gctgataaaggaccc[A/G]tatccaaaataggca | 5336 |
| rs4889388 | snp | A/G | 0.114387 | 0.210022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805192 | ccatatccaaaatag[A/G]caactcttaaaactc | 5336 |
| rs4889389 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81807596 | tgcttacttaattcc[A/T]caactgtatgtgttc | 5336 |
| rs4889393 | snp | A/G | 0.111576 | 0.20818 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810408 | TTATTTGCAGCATCA[A/G]TATTGGTGAATTTGC | 5336 |
| rs4889394 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812992 | atggtggtagatgtg[C/T]gatgttatttctgag | 5336 |
| rs4889395 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813032 | ctgttgcaatggtct[A/G]tatatctattttggt | 5336 |
| rs4889396 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813070 | ccatgctgttttgtt[G/T]accatagccttgtag | 5336 |
| rs4889397 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813151 | agggttgtcttggtt[A/G]tgtggtctctttttt | 5336 |
| rs4889398 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813157 | gtcttggttatgtgg[G/T]ctcttttttggttcc | 5336 |
| rs4889399 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813525 | attgattttgtatcc[C/T]gagactctgctgaaa | 5336 |
| rs4889400 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816050 | ctgggtgacagagca[A/T]gacttcatctttaaa | 5336 |
| rs4889401 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816088 | aaaaaTGTGCCTTCA[C/T]ggacaggcacgatgg | 5336 |
| rs4889402 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816262 | tgtaatcccagctac[G/T]tgggaggcagaggtg | 5336 |
| rs4889403 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816652 | CCCAGCTAATTTTAA[C/T]TTTTTTTTTTTTTTT | 5336 |
| rs4889406 | snp | C/G | 0.106633 | 0.204807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818131 | ACAGGGCTCTCGTGA[C/G]TATTCAGCCAGCTAG | 5336 |
| rs4889407 | snp | C/G | 0.488905 | 0.0736498 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820915 | tgcacaccatcatgc[C/G]tggctaatttttgtg | 5336 |
| rs4889408 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829815 | CCTTTCTCCTTTGAA[A/G]TTGCAGAGGGTGCTG | 5336 |
| rs4889409 | snp | C/G | 0.488057 | 0.0763479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832981 | GCCATGACAGTAACT[C/G]AGGGAAACAAGTCAC | 5336 |
| rs4889410 | snp | C/T | 0.127599 | 0.217986 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844042 | AGTGCAGTGGTGTGA[C/T]GTCGGCTCACTACAA | 5336 |
| rs4889411 | snp | C/T | 0.394538 | 0.203982 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849829 | TTGAAGACATTTTAC[C/T]GGGAAAGAGAATTGT | 5336 |
| rs4889412 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853030 | GAAGGTACCAGGCCT[C/T]CTTAAGTATTAGGCC | 5336 |
| rs4889413 | snp | C/G | 0.373196 | 0.217538 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853232 | gctactcctgaggct[C/G]aggcaggataattgt | 5336 |
| rs4889414 | snp | C/G | 0.371177 | 0.218669 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853266 | aacctgggaggcaga[C/G]gttgcagtgagctga | 5336 |
| rs4889415 | snp | A/G | 0.492679 | 0.0600586 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853344 | tcaaaaaaaaaaaac[A/G]aaacaacaaaaaaaa | 5336 |
| rs4889416 | snp | C/G | 0.309401 | 0.24284 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861610 | TGGATCAAATGAGGT[C/G]CTTGTGTTGGAAGAT | 5336 |
| rs4889417 | snp | C/G | 0.355954 | 0.226437 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862289 | GCTTGGCCCAAGCAC[C/G]CTGTTTCATTTTTTG | 5336 |
| rs4889418 | snp | A/G | 0.484421 | 0.0868729 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866669 | CACTGGGGCACCAGC[A/G]TGAGAGGACGCTGGC | 5336 |
| rs4889419 | snp | A/G | 0.330947 | 0.236533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869385 | TTGCCTTTGAGTTCC[A/G]TGGAATAGTGCACAA | 5336 |
| rs4889420 | snp | A/G | 0.499713 | 0.0119774 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869450 | AGACAGAGGGATCAT[A/G]GACATATCTGAGGAC | 5336 |
| rs4889421 | snp | A/T | 0.487368 | 0.0784625 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869710 | CAAGTCCTGGTAGTG[A/T]AGCTGTCAGAGTTGG | 5336 |
| rs4889422 | snp | C/T | 0.3512 | 0.228601 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869738 | TGGCTCTTTTTTCTT[C/T]TGTTTCTCCAACCAT | 5336 |
| rs4889423 | snp | A/G | 0.415563 | 0.18732 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881664 | TAGTATGTATATTCG[A/G]GACGGAGCCTCCCTT | 5336 |
| rs4889424 | snp | A/C | 0.487933 | 0.0767327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890366 | TTAGCTTGGCCCAAG[A/C]CCAGGAATAATTAAG | 5336 |
| rs4889425 | snp | C/T | 0.261056 | 0.249755 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890449 | CACTGTCATAATTTT[C/T]TTGTTGTTCTGATTT | 5336 |
| rs4889426 | snp | C/T | 0.465158 | 0.127307 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890509 | CTCTTCTCTACTGAC[C/T]GTGTTGCCTGGGTGG | 5336 |
| rs4889427 | snp | A/T | 0.399073 | 0.200692 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891157 | AACAGAGCATGACTC[A/T]GTGTGAAAAAACAAA | 5336 |
| rs4889428 | snp | C/T | 0.127944 | 0.218179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891389 | GAGCTGTTCTTCCCC[C/T]CTGGTGGGCGCAGAC | 5336 |
| rs4889429 | snp | A/G | 0.470618 | 0.117591 | intron-variant | PLCG2 | GRCh38.p7 | 16:81891832 | GCTAGTAAAAACAAA[A/G]GTAACTTAGTTTATG | 5336 |
| rs4889430 | snp | C/G | 0.227664 | 0.249 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893612 | AGCTTTGGCGGCTCG[C/G]GCGGAGAAGTTCCCC | 5336 |
| rs4889431 | snp | C/T | 0.47709 | 0.104548 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894643 | TGTGAGAGGTCGAGG[C/T]GGGCGGATCACTTGA | 5336 |
| rs4889432 | snp | A/G | 0.42666 | 0.176893 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898560 | TTTATTTTCACATTT[A/G]CCTTCATTTCTATTG | 5336 |
| rs4889433 | snp | C/T | 0.455383 | 0.142541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899163 | cattgcactccatcc[C/T]gggcaatgagtgaaa | 5336 |
| rs4889434 | snp | C/T | 0.49655 | 0.04139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899291 | ATATATATATATATA[C/T]ACACACACACACATA | 5336 |
| rs4889435 | snp | A/T | 0.229136 | 0.249128 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901833 | TGAAGAAACCCATCT[A/T]TTAGTGTATTGCAAA | 5336 |
| rs4889436 | snp | A/G | 0.225301 | 0.248777 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902237 | TTGTTGACATTCCAC[A/G]AGCTCATGGGGAAGG | 5336 |
| rs4889437 | snp | A/T | 0.228842 | 0.249103 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902566 | gcaccattcccattg[A/T]tgagagctctaccct | 5336 |
| rs4889438 | snp | G/T | 0.132066 | 0.220435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902595 | ctcatTCCCATTCAC[G/T]GGAGCTCTACTCTCA | 5336 |
| rs4889439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914531 | ATTCAGTTTGTGAGC[C/T]TGTCTTCCCCATGAG | 5336 |
| rs4889441 | snp | C/G | 0.447421 | 0.153379 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918689 | GATAGTGTGCTATCT[C/G]CAGCTTTGTTATTTT | 5336 |
| rs4889442 | snp | G/T | 0.442113 | 0.159977 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928268 | GTCTAGGATGTGTTT[G/T]GAAACCAGATCTGAG | 5336 |
| rs4889443 | snp | C/G | 0.191775 | 0.243125 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941066 | ACATAAAAAAATACA[C/G]TCTTTTGATATTGTT | 5336 |
| rs4889444 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941149 | CATTCCCTCAACTTC[C/T]ACCTTTTTTTGTATA | 5336 |
| rs4889445 | snp | A/G | 0.427727 | 0.175821 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941275 | CTCACTCCTGTAATC[A/G]TAATCCCAGCTACTT | 5336 |
| rs4889446 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943580 | TAGATTTCTTCACCA[A/C]TGTCCACAGATTagc | 5336 |
| rs4889447 | snp | C/T | 0.106987 | 0.205054 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948886 | GGTACACACCTGGAA[C/T]AGATGGCTGGCAGTT | 5336 |
| rs4889448 | snp | C/T | 0.467642 | 0.123012 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951990 | CTTGTATTTATTGAA[C/T]GTAACCACTTCTGTC | 5336 |
| rs4993826 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947777 | TTGTTTAGTTTATAA[A/G]GAGTATTTTTAGCAC | 5336 |
| rs4996272 | snp | C/T | 0.29175 | 0.246489 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940183 | CACTGTAAAACCGAT[C/T]GGGTGGCTTGGAGAG | 5336 |
| rs4997769 | snp | C/T | 0.499563 | 0.0147699 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871897 | tatggtctatccata[C/T]tatgtgacattatgc | 5336 |
| rs4997770 | snp | A/G | 0.499551 | 0.0149693 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871890 | ggtaaattatggtct[A/G]tccatattatgtgac | 5336 |
| rs4997771 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871804 | TATATTATCGgattg[C/T]ttattgcagcattac | 5336 |
| rs4997772 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871690 | ATTTTTTGATTAAAA[C/T]AATAGACTATTTAAA | 5336 |
| rs4997773 | snp | A/G | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871646 | cccagccCTTTATAT[A/G]CTTTTATTCATATTT | 5336 |
| rs4997774 | snp | C/G | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871580 | taacctcaactgatc[C/G]gcccgcctccacttc | 5336 |
| rs4997775 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871538 | agatggggttttgcc[A/G]cattgggtgggcagg | 5336 |
| rs4998545 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855872 | GGAGCGAATGTCTGA[C/T]TGATGATATGGAGGG | 5336 |
| rs5006644 | snp | G/T | 0.471673 | 0.115589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805772 | GTTTTGTTTTGTTTT[G/T]TTTTTTTTTTGTTTT | 5336 |
| rs5006645 | snp | C/G | 0.402806 | 0.197864 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805886 | CTCAAGTGATCCTCC[C/G]AGCTCAGCCTCCTGA | 5336 |
| rs5014001 | snp | C/G | 0.324855 | 0.23853 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881331 | TAACTGAATTAAAAT[C/G]AGTTCAGGTGTATAA | 5336 |
| rs5016604 | snp | A/C/G | 0.497717 | 0.0539243 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858443 | CTACAGGGGGGAAAA[A/C/G]AAAAAAAAGGGACAT | 5336 |
| rs5021608 | snp | A/C | 0.397452 | 0.201886 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824286 | TTATAGGCATGCGTC[A/C]CCACACCTGGCTAAT | 5336 |
| rs5818351 | in-del | -/TTTA | 0.489376 | 0.0721049 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778815 | TATTTATTTTTAATT[-/TTTA]TTTATTTATTTATTT | 5336 |
| rs5818352 | snp | G/T | 0.471673 | 0.115589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805783 | TTTTTTTTTTTTTTT[G/T]Ttttttttttttttt | 5336 |
| rs5818353 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81827197 | TTGCTGGGTTTTTTT[-/T]TTTTTTGGGGACAGG | 5336 |
| rs5818354 | in-del | -/C | 0.396364 | 0.202676 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838086 | AAAGATACTAATTTT[-/C]TTTTTTTTTTGAGGC | 5336 |
| rs5818355 | in-del | -/T | 0.379354 | 0.213933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854096 | CTCTTGTTTTTTTTT[-/T]GGTAGAATAGTCTGT | 5336 |
| rs5818356 | in-del | -/AAGCAGG | 0.400147 | 0.19989 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858090 | CCCATCTCAGACAAA[-/AAGCAGG]TCCTAGGGCCATGAC | 5336 |
| rs5818357 | in-del | -/GGA | 0.495095 | 0.0492773 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858437 | CATGGGCTACAGGGG[-/GGA]AAAAAAAAAAAAGGG | 5336 |
| rs5818358 | in-del | -/CT | 0.494272 | 0.053207 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888038 | TATTTGGAGCTGAGA[-/CT]CTGCAGTTTACAAGC | 5336 |
| rs5818359 | in-del | -/A | 0.475702 | 0.107512 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892652 | AACTTAAAAAAAAAA[-/A]CTTTTATTTTCAGTT | 5336 |
| rs5818360 | in-del | -/TAA | 0.343924 | 0.231686 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906084 | TTCTCCAAATATTAT[-/TAA]TAACATCCTACATAA | 5336 |
| rs5818361 | in-del | -/TAAG | 0.434976 | 0.168179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928035 | TTCTGCCACCTCTCC[-/TAAG]CCCAGGATATTCTTC | 5336 |
| rs5818362 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81941709 | AACTCCCCCTTTTTT[-/T]TTTTTTGAGATGGAG | 5336 |
| rs6420427 | snp | C/T | 0.460252 | 0.135255 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818702 | GGCAGCAGGAAATGG[C/T]TGAAATAACTTCCAT | 5336 |
| rs6564917 | snp | A/G | 0.336474 | 0.234568 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782756 | AAAATCCCACAAAAC[A/G]ATTCTGTTAAAATGG | 5336 |
| rs6564918 | snp | A/C | 0.342582 | 0.232225 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782914 | GCAGGTGAGAGTGTA[A/C]ATTCCACCCCTGCTC | 5336 |
| rs6564919 | snp | C/G | 0.342134 | 0.232404 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782975 | AAGCAATTGGTGAGA[C/G]GCAGCATGGAAGTCT | 5336 |
| rs6564920 | snp | A/C | 0.497241 | 0.037038 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785455 | TTTGCCAAAGTCTCC[A/C]TGGATGATTCTGAAG | 5336 |
| rs6564923 | snp | C/T | 0.315758 | 0.241197 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826221 | TCATTTCTGGCATCA[C/T]GTCCACCTCCTGGTT | 5336 |
| rs6564924 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PLCG2 | GRCh38.p7 | 16:81836959 | GTTTCCCTTCCCTTT[C/T]CTCCTGTTTGGTTTT | 5336 |
| rs6564925 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837098 | GTAGTTGTCTGTATT[C/T]TGAGAACCTTTCTCT | 5336 |
| rs6564928 | snp | G/T | 0.347253 | 0.230308 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883494 | CATGGAACGATTGCA[G/T]TCTGCCAGATGCCAG | 5336 |
| rs6564932 | snp | A/G | 0.468148 | 0.122112 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899580 | ttcctggtctacagc[A/G]tgaaagcttcaacaa | 5336 |
| rs6564933 | snp | C/T | 0.440746 | 0.161604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900442 | CCCAAGACTTGTGCC[C/T]TCACACCCAGGATGA | 5336 |
| rs6564934 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902732 | cattctcacactgct[C/T]ataaagacataccca | 5336 |
| rs6564935 | snp | G/T | 0.322959 | 0.239117 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905115 | tggtctagaactcct[G/T]agctcaagtgatctg | 5336 |
| rs6564936 | snp | A/G | 0.183886 | 0.241099 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905184 | gagccactgcgcctg[A/G]ccagtatgggcaatt | 5336 |
| rs6564938 | snp | A/C | 0.415563 | 0.18732 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926892 | CCCCAGTAACTCATT[A/C]GTAATTAAAAAATAA | 5336 |
| rs6564940 | snp | A/G | 0.247621 | 0.249989 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930199 | TAAAATAAAGATGCA[A/G]TACATGTAATCTGCT | 5336 |
| rs7184201 | snp | C/T | 0.183886 | 0.241099 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905182 | gtgagccactgcgcc[C/T]gaccagtatgggcaa | 5336 |
| rs7184243 | snp | A/G | 0.333491 | 0.235646 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854739 | CCCCTTTCTAGCTGT[A/G]TGTCTTTAGGTGAGT | 5336 |
| rs7184247 | snp | A/G | 0.482831 | 0.0910472 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874147 | AAATTAATTGCCTAC[A/G]TTTAAAACTTGAGAG | 5336 |
| rs7184713 | snp | A/G | 0.0101008 | 0.0703445 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942979 | GGGACTTGGGCAGCG[A/G]GAGAAGGTACATAGA | 5336 |
| rs7185099 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81796742 | gacagatacagaaat[C/T]tgagtcatgcatctg | 5336 |
| rs7185362 | snp | A/G | 0.338976 | 0.23363 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855300 | GTCCTGAGATCTTCT[A/G]TTGCACACACACATG | 5336 |
| rs7186146 | snp | C/G | 0.333491 | 0.235646 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854973 | CCAGCACTTTGGGAG[C/G]CTGAGGCGGGCAGAT | 5336 |
| rs7186381 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81862014 | CCCTGCTCTCTGTCA[A/G]CATGTGGAAAATCCC | 5336 |
| rs7186586 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81855255 | TTCCAGCAGATGTGG[C/T]TCAGCAAATCTGATT | 5336 |
| rs7186962 | snp | A/C/G | 0.461108 | 0.230926 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885492 | TTATTTCATCCACTT[A/C/G]TAACTTTACACTCCT | 5336 |
| rs7187163 | snp | C/T | 0.499693 | 0.0123764 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871177 | TTCCTGGTGGAAATG[C/T]GAATGGCCATAAGTT | 5336 |
| rs7187837 | snp | A/T | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871172 | ATGCCTTCCTGGTGG[A/T]AATGCGAATGGCCAT | 5336 |
| rs7187863 | snp | A/G | 0.238749 | 0.249747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81931372 | GTAGACGTCCCCATC[A/G]GTGCTAACCGTGGTC | 5336 |
| rs7188227 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815195 | CAGAGGGTGGTTATG[A/C]GAAGGGAGGAGGTTT | 5336 |
| rs7188344 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81822490 | ggctgggggcagtgg[C/T]tcatgcctgtaatcc | 5336 |
| rs7188361 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81888664 | acggtatgtaacttg[C/T]ccaaggtcaactagg | 5336 |
| rs7188577 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866608 | GCTCCACTGGGGCAC[C/T]AGCATGAGAGGATGC | 5336 |
| rs7188588 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866621 | ACTAGCATGAGAGGA[C/T]GCTGGCCTCTCCCTT | 5336 |
| rs7188701 | snp | C/G | 0.322007 | 0.239405 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883578 | TGTCGGGCCTCTTTT[C/G]AAGGCACACATTGAG | 5336 |
| rs7188868 | snp | A/G | 0.293551 | 0.246177 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852530 | CAGAGTTCACTGGTC[A/G]TCTTGTAGGGGGAAG | 5336 |
| rs7189106 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874126 | CTAATGGTTTAAATA[C/T]GTTAAAAATTAATTG | 5336 |
| rs7189462 | snp | G/T | 0.498182 | 0.0300969 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874262 | CATGGAACGGTCCAC[G/T]TTCTCTGTATTGACC | 5336 |
| rs7189468 | snp | C/G | 0.286564 | 0.247312 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788904 | TCCCTTCCCCCACAA[C/G]GGGTGAGAGGGTTGG | 5336 |
| rs7189727 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876857 | CTCCACGGTGCACCC[A/G]TAGCATCTAGAATAT | 5336 |
| rs7189764 | snp | C/G | 0.127944 | 0.218179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907018 | actccagcctggtga[C/G]agagacagactctgt | 5336 |
| rs7189843 | snp | C/G | 0.488241 | 0.0757703 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868534 | TGGCAGGTAGAGTCA[C/G]TAGGAGTCTTGTTCA | 5336 |
| rs7190115 | snp | A/G | 0.113169 | 0.214536 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831496 | aaactggccctctct[A/G]tttgtctcagtttta | 5336 |
| rs7190141 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877087 | ACTGAGACTGTCACC[A/G]TCTTGCCCCAGCTCA | 5336 |
| rs7190729 | snp | C/T | 0.347694 | 0.230122 | intron-variant | PLCG2 | GRCh38.p7 | 16:81906805 | agcaccttgggaggc[C/T]gaggaaggcagatta | 5336 |
| rs7190882 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818504 | CCATTCTTCCTCTGC[G/T]TGCATCTTGGGGATA | 5336 |
| rs7191743 | snp | C/T | 0.333491 | 0.235646 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855038 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 5336 |
| rs7192070 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902247 | TCCACGAGCTCATGG[A/G]GAAGGACAAACAGCT | 5336 |
| rs7192115 | snp | C/T | 0.339203 | 0.233544 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855240 | ATGTAACCTGTTTTC[C/T]TCCAGCAGATGTGGC | 5336 |
| rs7192266 | snp | C/T | 0.330016 | 0.236849 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855269 | GCTCAGCAAATCTGA[C/T]TGATCTGAAGGAACT | 5336 |
| rs7192314 | snp | C/G | 0.335559 | 0.234904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877543 | gttggcagggccaca[C/G]ccctcggaaggctcc | 5336 |
| rs7192423 | snp | A/G | 0.398354 | 0.201224 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902368 | ttctggaggctggaa[A/G]ttcaaggtcagggtg | 5336 |
| rs7192509 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871069 | CATAAATGAGAATGA[C/T]GAAAGCATACCATTT | 5336 |
| rs7192535 | snp | A/T | 0.499673 | 0.0127754 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871106 | ATTAGATTGGCAAAA[A/T]TCTTTAACCATGACA | 5336 |
| rs7192724 | snp | C/G | 0.368938 | 0.219895 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924693 | AACCTCATTGCAAAC[C/G]AATTCATACCTAGAT | 5336 |
| rs7192774 | snp | A/G | 0.397813 | 0.201621 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877390 | gaacctggaggcgga[A/G]cttacagtgagccga | 5336 |
| rs7192802 | snp | C/T | 0.33875 | 0.233717 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783417 | CCCATTAACTCGTTT[C/T]GCTACTTTCTATCTG | 5336 |
| rs7193086 | snp | A/T | 0.448836 | 0.15154 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916092 | AAAATACAAATGGGA[A/T]CATTCTGCAGCTTTT | 5336 |
| rs7193093 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831772 | CCCCAATCCTGCCTT[C/G]TCTGAAAGGGAAGGA | 5336 |
| rs7193188 | snp | C/G | 0.40086 | 0.199352 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902061 | CAGAGCACGGGAAGT[C/G]CAAGGGTGTCCAGGG | 5336 |
| rs7193222 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823445 | TTGAGTGGGGGTAGG[C/G]GCTGCACTGTCTGAT | 5336 |
| rs7193477 | snp | A/T | 0.294064 | 0.246086 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852577 | GTCAGTCAGGTTGCT[A/T]TCCTTGCCTGGTAGG | 5336 |
| rs7193588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815128 | GATAATTGGGGAATT[C/T]AGGCTTAAAATGAAG | 5336 |
| rs7193967 | snp | A/C | 0.495521 | 0.0471118 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872373 | ATCCTCCTTTTGCTC[A/C]TTTTTATGAGCAAGG | 5336 |
| rs7194131 | snp | A/C | 0.132066 | 0.220435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831630 | AGGTAGATTTCAGCC[A/C]CAAGCTGTGGAGTCC | 5336 |
| rs7194366 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823288 | GTGAGCCCCTGTGGC[C/T]GGGGCAGCTGCAGCA | 5336 |
| rs7194497 | snp | C/T | 0.174932 | 0.238463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895553 | CAACAGAGCGAGACT[C/T]TGTCTTAAAAAAAAA | 5336 |
| rs7194672 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB, nc-transcript-variant | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777345 | AAATTATACATATAT[A/G]TGACTGAACTAATAT | 5336 |
| rs7194787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831591 | CTGGCTGGGTCTCTG[A/G]CCAGTGCTGGGAAAG | 5336 |
| rs7195005 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825547 | tgttccacctgcctc[A/G]gtctcccaaagtgct | 5336 |
| rs7195041 | snp | A/C | 0.489024 | 0.0732638 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777513 | CTGGGGAATTGGCCC[A/C]ATGACTTCAAGTGGT | 5336 |
| rs7195281 | snp | C/G | 0.499693 | 0.0123764 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868995 | CTACCCTGTGAGTCT[C/G]CTATGTGACCCATGT | 5336 |
| rs7195470 | snp | A/G | 0.422787 | 0.180679 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789721 | CCCCCGGATGGTCTG[A/G]TAACTAGGCAGGTTT | 5336 |
| rs7196329 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890517 | TACTGACCGTGTTGC[C/T]TGGGTGGGATTATTG | 5336 |
| rs7196410 | snp | A/C | 0.487933 | 0.0767327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868877 | CTCCAGTGTAGGTGC[A/C]TCCTCATTGGGGCAT | 5336 |
| rs7196412 | snp | A/G | 0.124144 | 0.21601 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850371 | CAAACAAACAAAAAA[A/G]TTTCAGTGCACGAAA | 5336 |
| rs7196695 | snp | C/T | 0.380919 | 0.21298 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868474 | CAGCTGGGTCTTTCC[C/T]GGCTGATTCTGCCAA | 5336 |
| rs7196831 | snp | C/T | 0.467946 | 0.122472 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789725 | CGGATGGTCTGGTAA[C/T]TAGGCAGGTTTCACA | 5336 |
| rs7196862 | snp | C/G | 0.0869089 | 0.189476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886751 | CATTTATATAACATG[C/G]AGAATAACCTGTACC | 5336 |
| rs7196980 | snp | A/G | 0.202035 | 0.245356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841162 | TTTTTAACAAAGAAG[A/G]TAAGGGCAGGCCCAC | 5336 |
| rs7197171 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924218 | TGATAGGTTTCTGGG[C/G]AAGTGGTTTTGTGGG | 5336 |
| rs7197601 | snp | A/C | 0.499437 | 0.0167637 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877580 | GGATGTGTTCCAGAC[A/C]TCTTTCATGGCTTCT | 5336 |
| rs7197677 | snp | C/G | 0.499784 | 0.0103811 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872732 | TACCTGGAACTTGGA[C/G]TCAGGTGGCTGTGGT | 5336 |
| rs7197685 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872740 | ACTTGGAGTCAGGTG[A/G]CTGTGGTTTCTGCAG | 5336 |
| rs7197689 | snp | C/G | 0.498034 | 0.0312882 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872752 | GTGGCTGTGGTTTCT[C/G]CAGTTAGCTGCATGA | 5336 |
| rs7197832 | snp | A/G | 0.499424 | 0.0169631 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872772 | TAGCTGCATGATCTT[A/G]GATGAACCACTGACT | 5336 |
| rs7198003 | snp | C/G | 0.213333 | 0.247296 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777792 | AGGCCAAGGTGGGTG[C/G]ATCACTTGAGGTCAG | 5336 |
| rs7198047 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902987 | aattacctcccactg[C/G]gttcctcctatgaca | 5336 |
| rs7198169 | snp | C/G | 0.240765 | 0.249829 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777852 | GAAACCGCGTCTCTA[C/G]TAAAAATACAAAAAA | 5336 |
| rs7198191 | snp | G/T | 0.489142 | 0.0728777 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777880 | AAATTAGCCAAGCAT[G/T]ATGGCATACACCTAT | 5336 |
| rs7198440 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903213 | AATAGGACACACAAG[G/T]GTGTGGTGGTGTCAA | 5336 |
| rs7198768 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856866 | gggttcttagatacc[C/T]gggaaggtcattccc | 5336 |
| rs7198813 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872588 | TGAGACTATTCTGTG[C/T]GATGCACCTAGCACA | 5336 |
| rs7198995 | snp | C/G | 0.489083 | 0.0730708 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777603 | tggtgatgagcacag[C/G]tatacacgccagttg | 5336 |
| rs7199267 | snp | A/T | 0.480223 | 0.0974544 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895134 | ATGACCCATTTCTGT[A/T]TGAAAATATTACTGT | 5336 |
| rs7199278 | snp | C/G | 0.158632 | 0.232706 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902930 | catgagatgtgttca[C/G]tatcacaagaacagc | 5336 |
| rs7199578 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872629 | GGTGGCACACATTCA[A/G]TAAGTAGGGGCTGCT | 5336 |
| rs7199605 | snp | C/T | 0.488965 | 0.0734569 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81777873 | ATACAAAAAATTAGC[C/T]AAGCATGATGGCATA | 5336 |
| rs7199820 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895580 | AAAAAAAAATGAAAA[A/G]AAAAGCAGCATTGAA | 5336 |
| rs7199941 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872818 | CTTCTCCTCTGTGCA[A/G]TGGGAGGTTGGGAGT | 5336 |
| rs7200056 | snp | C/T | 0.15698 | 0.23205 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903340 | CCGTCAACAGAGAAA[C/T]ACCAAACAGTGCAAG | 5336 |
| rs7200218 | snp | C/G | 0.388964 | 0.20782 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825907 | ATAGGGTGTTAGGTG[C/G]ATCGTAGAGAAAGAA | 5336 |
| rs7200324 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | PLCG2 | GRCh38.p7 | 16:81872995 | AGTTAGAGAAATGGG[A/G]GGGCCATTTCCTATC | 5336 |
| rs7200358 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903138 | ataaattttgggagg[A/G]cacagacattcagac | 5336 |
| rs7200626 | snp | C/T | 0.498369 | 0.0285077 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874699 | GTTCATGCTTATCAG[C/T]AGCCAAATGGTTTCC | 5336 |
| rs7200783 | snp | C/G | 0.495745 | 0.0459295 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874766 | CCTGCCTACGTTCCA[C/G]CTCTCGAGCTTCAGA | 5336 |
| rs7201045 | snp | A/G | 0.365439 | 0.221752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926347 | CTGGCTGCGGAAAAT[A/G]GCTCAAGAGATGGGC | 5336 |
| rs7201402 | snp | C/T | 0.460477 | 0.134905 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840928 | GGTCCCTTCCTCCCT[C/T]GGGGATGGGGAGTCC | 5336 |
| rs7201405 | snp | G/T | 0.460813 | 0.134379 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840934 | TTCCTCCCTTGGGGA[G/T]GGGGAGTCCCAGAGG | 5336 |
| rs7201504 | snp | G/T | 0.231775 | 0.249335 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957720 | CACATTATTCTCATT[G/T]AATCTTCATGTCAGC | 5336 |
| rs7201531 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825298 | Atttttttttttttt[G/T]ttttttttgagacag | 5336 |
| rs7201604 | snp | A/G | 0.401215 | 0.199083 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850731 | TGGCACCTGCACAGT[A/G]TAACAGCATAGAGAG | 5336 |
| rs7201677 | snp | C/T | 0.155987 | 0.23165 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890900 | gggtgcagtggctca[C/T]gcctgtaatcccagc | 5336 |
| rs7202169 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890788 | ATTTCCTGCCCTTTC[A/G]ACATTCTGATATGGA | 5336 |
| rs7202174 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820887 | cagcctcctgagtag[G/T]tgggattacaggtgc | 5336 |
| rs7202205 | snp | A/G | 0.271432 | 0.24908 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851034 | CAGCTTGTAGTAGAA[A/G]TCCTCAGTGGGGTGT | 5336 |
| rs7202250 | snp | C/T | 0.498392 | 0.028309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868965 | GAGACCAGCCCTCCT[C/T]ATTGGGGCATCACCC | 5336 |
| rs7202665 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81957597 | GGGGTGCGGGGCGGC[C/T]GGGGTTGCCAAGTGT | 5336 |
| rs7202834 | snp | C/T | 0.343701 | 0.231776 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789852 | CACCTTTGCCCCCCC[C/T]CCATTGCCTCCCCTC | 5336 |
| rs7203405 | snp | C/T | 0.414741 | 0.188044 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878036 | acccaggctggagtg[C/T]agtggcgccatctcg | 5336 |
| rs7203619 | snp | C/T | 0.486133 | 0.082104 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923904 | TTGCTTTCCATGCAT[C/T]GTCTAACCAAATCTT | 5336 |
| rs7203893 | snp | A/G | 0.495963 | 0.0447464 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830199 | ttggcacgcatctgt[A/G]gtcccagctacttag | 5336 |
| rs7204115 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930344 | GAGAACCCACGCCAC[A/G]TTTCTCTCCTAGTTT | 5336 |
| rs7204457 | snp | G/T | 0.00952359 | 0.0683454 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866580 | CGTGGCCTCTCCCTT[G/T]CTCCCAAGATGAGCT | 5336 |
| rs7204645 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851224 | cctggcaaaaatagt[A/G]cagtttctgtgaacc | 5336 |
| rs7204834 | snp | A/G | 0.110519 | 0.207473 | intron-variant | PLCG2 | GRCh38.p7 | 16:81821239 | gggattcagtgagtt[A/G]acatgtgagtgatta | 5336 |
| rs7205202 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830192 | aggcatgttggcacg[C/T]atctgtggtcccagc | 5336 |
| rs7205376 | snp | C/T | 0.220246 | 0.248223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948237 | AGTAAATAGTTTCTC[C/T]TAAGTTGTCGTATTA | 5336 |
| rs7205843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793901 | CTTGTTCTTCCCAGT[C/T]TCAGTCTCAAGTCTT | 5336 |
| rs7206344 | snp | C/G | 0.48679 | 0.0801892 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888515 | GCACTTTCTGTGCAC[C/G]AGGTGCTGCATTAGG | 5336 |
| rs7206437 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848416 | GTGTGCGGATGTGCA[A/G]GGCTGCTTGTATCAT | 5336 |
| rs7206563 | snp | A/T | 0.429238 | 0.174281 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866646 | TCCCTTGCTCCCAGG[A/T]TGAGCTCCACTGGGG | 5336 |
| rs7206632 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818398 | tcagctctttgaaag[A/G]gggctgtttgttcca | 5336 |
| rs7206834 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888388 | gctgatttaaagaaa[A/C]aaaaaatgtttgtat | 5336 |
| rs7342692 | snp | G/T | 0.277334 | 0.248501 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870119 | TCCACATTAATCCAA[G/T]AATAGAAAAAGAGAA | 5336 |
| rs7342694 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870195 | TGATTGCTACACAGT[C/T]GCCATTTAATTCTTT | 5336 |
| rs7350826 | snp | A/G | 0.473174 | 0.112665 | intron-variant | PLCG2 | GRCh38.p7 | 16:81840309 | CAGAGCAGCAGTCCC[A/G]GACTTTTTTGGCACC | 5336 |
| rs7404289 | snp | C/T | 0.335101 | 0.23507 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782625 | ATTCATGTTCTTGTA[C/T]CTCACAAGCTTATTT | 5336 |
| rs7404552 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81815923 | aaaaattagccaggc[A/G]tggtgacttgcgcct | 5336 |
| rs7404636 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811552 | aggccccagtgtgtg[A/G]tgttcccctccctgt | 5336 |
| rs7405072 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811674 | ggtttccagcttcat[C/G]catgtccctgcaaag | 5336 |
| rs7405096 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811873 | gatttacaatccttt[C/T]ggtttatacccagta | 5336 |
| rs7405099 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811928 | tttctggtgctagat[A/C]ctcgaggaattgcaa | 5336 |
| rs7405103 | snp | C/T | 0.117886 | 0.21224 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811954 | tgcaacgctgtcttc[C/T]acaatggttgaactg | 5336 |
| rs7405168 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811942 | tcctcgaggaattgc[A/C]acgctgtcttccaca | 5336 |
| rs7499005 | snp | G/T | 0.484421 | 0.0868729 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827807 | AAAAAAAGCGTTGAC[G/T]CCgccaggcacggtg | 5336 |
| rs7499232 | snp | C/T | 0.17461 | 0.238362 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930934 | TTTTTAAAATGAACA[C/T]GTATTGTTTTAGTAA | 5336 |
| rs7499275 | snp | A/C | 0.488057 | 0.0763479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827778 | AGGTTGTTACTGTGA[A/C]ATCTCCTCATTTAAA | 5336 |
| rs7499440 | snp | A/C | 0.300673 | 0.244811 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932442 | TGTTCTTGTGGCTGC[A/C]GAACTGGAAAGAAAT | 5336 |
| rs7499585 | snp | G/T | 0.499368 | 0.0177603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780821 | CACTTGAGGTCAAGC[G/T]TTCCAGACCAGCCTC | 5336 |
| rs7500286 | snp | A/G | 0.47934 | 0.0995154 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932590 | TCCTCCAAGATAGTC[A/G]CCCACCAGTGGCCAG | 5336 |
| rs7500467 | snp | A/G | 0.314301 | 0.241589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853767 | AGGGCAGCTGGCTAT[A/G]TAAGGCATAAATACT | 5336 |
| rs7500567 | snp | C/T | 0.139225 | 0.224118 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904994 | ccaggttcaagcaat[C/T]ttactgtctcagcct | 5336 |
| rs7500570 | snp | C/T | 0.143622 | 0.226238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905032 | agctgggattacagg[C/T]gcgtgccaccatgcc | 5336 |
| rs8043593 | snp | G/T | 0.44252 | 0.159487 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842674 | GTTCCTGGTGTCAGG[G/T]GTGGGAGGACGTTCC | 5336 |
| rs8043619 | snp | C/T | 0.435119 | 0.16802 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935831 | TCCCAAGATCTTCTC[C/T]TACCCAAAACCATTC | 5336 |
| rs8043706 | snp | C/T | 0.158632 | 0.232706 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833615 | gctcactgtaccttc[C/T]acctcctaggatcaa | 5336 |
| rs8043845 | snp | C/T | 0.242201 | 0.249878 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787926 | tttgtggcagaatca[C/T]gatacgttgtatggg | 5336 |
| rs8043949 | snp | A/C | 0.460027 | 0.135605 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882706 | TCTGGTTTCCTTGCC[A/C]GGTACTCTCTGCACC | 5336 |
| rs8044282 | snp | C/G | 0.141596 | 0.225274 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826660 | TTAACCACGTCCTCT[C/G]AGTGGTCTTATTAAC | 5336 |
| rs8044333 | snp | C/G | 0.0766824 | 0.180169 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861632 | TTGGAAGATTTGGTA[C/G]ACACTGGTCTCTTTC | 5336 |
| rs8044681 | snp | A/C | 0.0726307 | 0.176182 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826930 | TGGAGATCCGCAGAA[A/C]CAGCCTCCTGCCTCC | 5336 |
| rs8045054 | snp | A/G | 0.365646 | 0.221644 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879570 | GATAGTCCCCATGAC[A/G]TCCTGGGCTGCAAGG | 5336 |
| rs8045609 | snp | A/T | 0.107341 | 0.205301 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805226 | aataaaaggccaggc[A/T]cggtagctcatgcct | 5336 |
| rs8045964 | snp | C/T | 0.49925 | 0.0193488 | intron-variant | PLCG2 | GRCh38.p7 | 16:81783128 | TGTCCTGGTTTCTGT[C/T]TAATTGAAGGTGTTA | 5336 |
| rs8047206 | snp | A/C | 0.484771 | 0.0859212 | intron-variant | PLCG2 | GRCh38.p7 | 16:81785017 | AGGATCCTTCTGGCT[A/C]TGCATCTGAGAATTG | 5336 |
| rs8047356 | snp | A/G | 0.232943 | 0.249417 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949494 | GTGGACTAGGAAGAC[A/G]GAATAATTCAGTGTC | 5336 |
| rs8047417 | snp | A/T | 0.36606 | 0.221428 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822108 | TTTCTTCCTTTTTCA[A/T]TTTTATCCTCTGTGC | 5336 |
| rs8047437 | snp | C/G | 0.273587 | 0.248885 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830916 | GATGGACAGGCACTG[C/G]GGGTCATGAGGGTTT | 5336 |
| rs8047444 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | PLCG2 | GRCh38.p7 | 16:81830943 | GTTTCAGAGAGCATA[C/T]GCAGTGTGTCCCAGC | 5336 |
| rs8047633 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PLCG2 | GRCh38.p7 | 16:81831031 | TGCATTTACTATTTG[C/T]TCTGCCTGAAATATT | 5336 |
| rs8047817 | snp | G/T | 0.108048 | 0.20579 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928083 | CTGGGATGGTTCAAG[G/T]GTGCAATGGGAGGCA | 5336 |
| rs8048100 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896927 | CTCAGGTGTAATCCT[C/T]TTCTGTCCCACCAGA | 5336 |
| rs8048389 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845490 | tgaagttactgtcca[A/G]agctatctgctataa | 5336 |
| rs8048471 | snp | C/T | 0.458084 | 0.138567 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882709 | GGTTTCCTTGCCAGG[C/T]ACTCTCTGCACCTCC | 5336 |
| rs8049024 | snp | G/T | 0.438526 | 0.164189 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884265 | ctgaggcaggagaat[G/T]gcttgaacctgggag | 5336 |
| rs8049305 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897798 | gatcctcccgcctca[A/G]cctcccaaagtgtgg | 5336 |
| rs8049604 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861686 | TGACTTTTCTTTCTC[G/T]GTGGCTTATGATGAT | 5336 |
| rs8050257 | snp | A/C | 0.49962 | 0.0137727 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952896 | tatcaattagaaaga[A/C]aaaaatagcagcttt | 5336 |
| rs8050292 | snp | A/C | 0.483272 | 0.0899109 | intron-variant | PLCG2 | GRCh38.p7 | 16:81849390 | GGAAGACAATGTTAC[A/C]TTGTCTAAAAAAGTT | 5336 |
| rs8050528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81932109 | CGGTTCTTTCCGGTG[A/G]AGGAACTTCCCCTCT | 5336 |
| rs8050597 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81922985 | GTAGATAGGGGACTG[C/G]TGACCTACAAAAACA | 5336 |
| rs8051199 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837378 | ACGAGTGGGCACCCT[A/G]CAGGCCACTTCCTCT | 5336 |
| rs8051345 | snp | A/T | 0.157972 | 0.232445 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901226 | CAGCTTCCAGTTGTG[A/T]GGGAGGCGGGCAGTT | 5336 |
| rs8052218 | snp | A/G/T | 0.582026 | 0.106045 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784001 | CAGATTAAATTTAGG[A/G/T]TTCCTTCTTGCTGCT | 5336 |
| rs8052319 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837032 | GTTCTCCATGGGAAG[A/G]CTCAACATCAGTTAC | 5336 |
| rs8052576 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837531 | GTAAGGGATGCTCTC[C/T]GCAGGGACCCCCGTG | 5336 |
| rs8053021 | snp | A/C | 0.125874 | 0.217008 | intron-variant | PLCG2 | GRCh38.p7 | 16:81911199 | AAGCTGCAAAAATGT[A/C]CATTTCCGAGGAGGC | 5336 |
| rs8053344 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PLCG2 | GRCh38.p7 | 16:81881263 | TTTTTTTTTTAATTA[C/G]AAAAACTAATGTTAA | 5336 |
| rs8053418 | snp | C/T | 0.153997 | 0.230832 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949433 | CTAATATCAGACTTG[C/T]CCTCTTTGGTGCTGA | 5336 |
| rs8053636 | snp | C/T | 0.424659 | 0.17887 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897757 | actatgttggccagg[C/T]tggtcttgaactcat | 5336 |
| rs8054878 | snp | A/G | 0.473174 | 0.112665 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828767 | TGATTGAACAATGTG[A/G]CATTTTCCTGAGTGC | 5336 |
| rs8054962 | snp | A/G | 0.473909 | 0.111197 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950457 | ACAACTGTATAAAGA[A/G]AAAATCTTTCAGAAT | 5336 |
| rs8055043 | snp | G/T | 0.465788 | 0.126237 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946833 | TAATTTAGCTGAATG[G/T]TAAAACTGTAAAACC | 5336 |
| rs8055576 | snp | G/T | 0.426354 | 0.177198 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886925 | TACCCTACACCAAGT[G/T]GATGCATTTTATAAC | 5336 |
| rs8055919 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790101 | CATTGGTGTCTACCC[C/T]ACAGGCTCATGGTTG | 5336 |
| rs8056205 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828814 | CATAGAAGGTTTCAA[C/T]AAATGTGAATTTATT | 5336 |
| rs8056564 | snp | C/T | 0.436123 | 0.166908 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946414 | AGAATTCCTTTTTGC[C/T]AATTCCCCAGAGTGT | 5336 |
| rs8056721 | snp | C/T | 0.480618 | 0.0965156 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829149 | agtctggctctgtca[C/T]ccaggctggagtgca | 5336 |
| rs8056796 | snp | A/C | 0.491577 | 0.0643472 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828827 | AACAAATGTGAATTT[A/C]TTTCCCCTTAACTTG | 5336 |
| rs8056821 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902594 | cctcatTCCCATTCA[C/T]TGGAGCTCTACTCTC | 5336 |
| rs8057026 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829263 | acatgcacacaccaa[C/T]gtgcccggctaattt | 5336 |
| rs8057305 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829066 | CCCTGTCTTTTTTGT[A/G]TCTGTGATTTTCATT | 5336 |
| rs8057373 | snp | C/G | 0.430434 | 0.173042 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887250 | TCAGCCTCCCGAGTA[C/G]CTGGGACTACAGGCA | 5336 |
| rs8057634 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81902463 | aaagggtgaggcagc[A/T]ctctgggacctcttt | 5336 |
| rs8057683 | snp | A/G | 0.497473 | 0.0354532 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829258 | ggattacatgcacac[A/G]ccaacgtgcccggct | 5336 |
| rs8058099 | snp | A/G | 0.495855 | 0.045338 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875067 | cttccgggttcaagc[A/G]attctcctgcctcag | 5336 |
| rs8058287 | snp | G/T | 0.495963 | 0.0447464 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875156 | tttaattgaaacggg[G/T]tttcaccgtgttggc | 5336 |
| rs8058290 | snp | A/G | 0.49533 | 0.0480965 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875164 | aaacggggtttcacc[A/G]tgttggccaggctag | 5336 |
| rs8058331 | snp | A/G | 0.495927 | 0.0449436 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875211 | tcaggtgatcctccc[A/G]ccttggcctcccaag | 5336 |
| rs8059316 | snp | C/T | 0.147991 | 0.228242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833040 | AGGGAAGTCCAGAAG[C/T]GGAAGGCAACCTCTC | 5336 |
| rs8059606 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81951066 | gatcatggctcactg[C/G]agccttgacctcctg | 5336 |
| rs8059924 | snp | A/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81832977 | TGGGGCCATGACAGT[A/C]ACTGAGGGAAACAAG | 5336 |
| rs8060444 | snp | C/G/T | 0.58 | 0.116619 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781870 | TCATGTCCTTTCCCC[C/G/T]CCCCCCCCCGCCCGC | 5336 |
| rs8060951 | snp | C/G | 0.465368 | 0.126951 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887607 | GCATGTCACCAGCCT[C/G]CTGGTCACCACCTGA | 5336 |
| rs8061071 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826391 | TAGGGGTCCATGGGC[A/G]GGTTCCCTGGGCTCC | 5336 |
| rs8061623 | snp | C/T | 0.496968 | 0.0388195 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828969 | TCCTGTGTGGGCCAT[C/T]CTCTCAAACATTGCT | 5336 |
| rs8061846 | snp | A/T | 0.480618 | 0.0965156 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829138 | ttttgagacggagtc[A/T]ggctctgtcacccag | 5336 |
| rs8062052 | snp | A/C/T | 0.0146728 | 0.0844358 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879063 | TACCTCTGCCATTGT[A/C/T]CGAGCTCCCTGAGTG | 5336 |
| rs8062268 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896764 | cccacctggggccag[A/G]ctctgtgctaggttc | 5336 |
| rs8062348 | snp | A/G | 0.093417 | 0.194889 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878900 | TGCGTCCCAGGGGCC[A/G]ATTCCTGCAAACACG | 5336 |
| rs8062633 | snp | C/T | 0.165527 | 0.235296 | intron-variant | PLCG2 | GRCh38.p7 | 16:81879378 | TAAATTACACATCAA[C/T]GAAAGGAAGTACTTC | 5336 |
| rs8062699 | snp | G/T | 0.474453 | 0.110094 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897045 | tgttgcaactattca[G/T]ccctgttgctgaagt | 5336 |
| rs8063063 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954967 | accgacagtgtaaaa[C/G]tgttcctatttctcc | 5336 |
| rs8063260 | snp | C/T | 0.39009 | 0.207062 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903929 | ATAGCGTTGGCCACA[C/T]GGTCACTTTGTACCA | 5336 |
| rs8063355 | snp | A/G | 0.380919 | 0.21298 | intron-variant | PLCG2 | GRCh38.p7 | 16:81883033 | TTGGAGCAGCTAAAT[A/G]TAGACACCAGGGCCT | 5336 |
| rs8063604 | snp | A/G | 0.42574 | 0.177808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926595 | ACTCAGCTTATGTTA[A/G]TTTAGAGTCCTAATA | 5336 |
| rs8063637 | snp | C/G | 0.410399 | 0.191761 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788067 | tgtctgtttttattt[C/G]ttttgggtatatacc | 5336 |
| rs8063728 | snp | A/G | 0.42574 | 0.177808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926658 | ATTTTTCAGATGGAG[A/G]GTTGGAGGCACAGAA | 5336 |
| rs8063813 | snp | A/G | 0.473266 | 0.112482 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948381 | ATGGGCAAACTGGCC[A/G]TTTCTGGAGGGCACA | 5336 |
| rs8182116 | snp | C/T | 0.223225 | 0.248562 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844876 | GAGTTTTTGTCATGT[C/T]GGTACATAAGGATCT | 5336 |
| rs9319571 | snp | C/T | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782110 | CTTGATCTCCTGACC[C/T]CATGATCCGCCCACC | 5336 |
| rs9673682 | snp | G/T | 0.468349 | 0.121752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846169 | TCTCACTAGAAGAAA[G/T]CTGCATCACCTAGGA | 5336 |
| rs9673861 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874956 | CCTATGTGTTTTTTT[G/T]TTTTTTTTTTTTTTT | 5336 |
| rs9674313 | snp | A/G | 0.444267 | 0.157354 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882183 | ACCCTGGGAAGCCCC[A/G]TGTAGCAGAATGTAC | 5336 |
| rs9674332 | snp | C/T | 0.306927 | 0.243432 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859635 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 5336 |
| rs9674362 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781892 | cccgcccgcccccga[A/G]acggagtcttgctct | 5336 |
| rs9674372 | snp | A/T | 0.140581 | 0.224783 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860221 | CCAGACATTTTTTTT[A/T]AAAAAAAGCAAACGC | 5336 |
| rs9674414 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812110 | gctggactgcagtgg[C/T]gctatctcagctcac | 5336 |
| rs9674416 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812135 | gctcactgcaagctc[C/T]gcctcctgggttcac | 5336 |
| rs9708320 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81813005 | tgtgatgttatttct[A/G]aggtctgtgttctgt | 5336 |
| rs9708339 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812717 | ttaattttgccattg[C/G]ttttggtgttttagt | 5336 |
| rs9746764 | snp | A/T | 0.359787 | 0.224604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878062 | tctcggctcactgca[A/T]gctctgcctcccggg | 5336 |
| rs9746892 | snp | A/G | 0.221141 | 0.248329 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812251 | agacgaagtttcacc[A/G]tgttagccaggatgg | 5336 |
| rs9746937 | snp | C/G | 0.227369 | 0.248974 | intron-variant | PLCG2 | GRCh38.p7 | 16:81812101 | tttgcccaggctgga[C/G]tgcagtggcgctatc | 5336 |
| rs9788863 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81816470 | TGAGAAGGAGACCTT[G/T]TCCCTCATTATAAtt | 5336 |
| rs9806889 | snp | A/G | 0.348794 | 0.229651 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811745 | tggtgtatatgtgcc[A/G]cattttctttatcca | 5336 |
| rs9806938 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810328 | TAGTCTATAGAACAC[A/G]TAACGTGGCCATGAG | 5336 |
| rs9806949 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810388 | GCATCTATGCTTGGC[C/T]Ttcgttatttgcagc | 5336 |
| rs9806951 | snp | C/G | 0.387832 | 0.208572 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810456 | tttgcaacctgcaaa[C/G]cagtagttctggccc | 5336 |
| rs9806965 | snp | C/G | 0.141934 | 0.225437 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811429 | CCTGAGAAGATGATG[C/G]ATTCCCTAGGCTGGG | 5336 |
| rs9806968 | snp | A/G | 0.445987 | 0.155207 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811503 | TAGGTATTTCTCCTA[A/G]TGCTATCCCTCCTCT | 5336 |
| rs9807001 | snp | C/G | 0.352504 | 0.228019 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811692 | tgtccctgcaaagga[C/G]atgagctcatccttt | 5336 |
| rs9921809 | snp | C/G | 0.4087 | 0.193169 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875793 | GAGAAGGCTGCTAAC[C/G]TATCTCTGGTTGTTC | 5336 |
| rs9922016 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873805 | AAAAAGAAGATTTGC[A/G]CAAAAGCTGTTTCAC | 5336 |
| rs9922182 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873951 | TGTCTATGAGGGAGA[A/T]ACATAAATTGGAATC | 5336 |
| rs9922196 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825678 | ctttaatggcaaaaa[C/T]tgtgacaacttttgc | 5336 |
| rs9922216 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943019 | AGCTGGTCATGAGGG[C/G]AGAGCTCATGTCTCC | 5336 |
| rs9922366 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874189 | TATTAAAATCTAGAT[A/T]TTTGGCTTCCCTTAG | 5336 |
| rs9923149 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835777 | gttggtagggcagtg[C/T]tcccgctggaggctc | 5336 |
| rs9923151 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827000 | CCTGGACTTGTTTCT[A/G]CTTCCAGCCTCCCTG | 5336 |
| rs9923199 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790771 | GGTGATTTTTGCCTC[C/T]CCCTCCCTACTCCAG | 5336 |
| rs9923424 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791056 | CCTGTTTGGATGGAA[C/T]TTTCTCATTTGTTCA | 5336 |
| rs9923780 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871431 | GCAACCTTTGCCTCC[C/T]GGGTTCAAGCGATTC | 5336 |
| rs9924101 | snp | C/T | 0.499325 | 0.0183582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873757 | CAACATAGTGAGACC[C/T]AGTCTGTATTATTAA | 5336 |
| rs9924213 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | PLCG2 | GRCh38.p7 | 16:81888875 | accatgcccatttgc[C/G]tacggatcatctgtg | 5336 |
| rs9924401 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889107 | GCGACTGGATGGACC[C/T]TGGGAAATGAAGAAT | 5336 |
| rs9924890 | snp | A/C | 0.211819 | 0.247067 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818742 | CCTTGTCATGAGTTT[A/C]CATGGAAACTGAGGG | 5336 |
| rs9925255 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914229 | ACTGAGGTGCCCAAG[C/T]GGTGAGACAGCTCTG | 5336 |
| rs9925328 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827126 | ATAAGACTCAGGGGA[C/T]GCCCCTCAACGGGAT | 5336 |
| rs9926920 | snp | C/G | 0.35207 | 0.228214 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825447 | gcatggcatgcgcca[C/G]cacacctggctagtt | 5336 |
| rs9928191 | snp | G/T | 0.498852 | 0.0239341 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953291 | GAATAAGATCTGTAG[G/T]TTTAGTATTGCACCG | 5336 |
| rs9928597 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896036 | CCTCCCTCCAAATGC[A/G]GGAAGGCCTGGGCCC | 5336 |
| rs9929503 | snp | C/G | 0.438806 | 0.163867 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926377 | CAGGTTGAAGGAGGG[C/G]GTTTGCATGTCTGGG | 5336 |
| rs9930054 | snp | C/T | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811010 | TGGCCTTCCTGGCCC[C/T]AGTGGCTGTGCTTTG | 5336 |
| rs9930295 | snp | A/G | 0.114738 | 0.210248 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790895 | GCTGTTAAATGTTCT[A/G]TAGTGCACAGGACAG | 5336 |
| rs9930647 | snp | C/G | 0.142609 | 0.225759 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790583 | GTTAGCAGGAACTTG[C/G]TGGTTACTGTGGGGT | 5336 |
| rs9930679 | snp | A/T | 0.084728 | 0.187577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899755 | gaaaacacctgtgtc[A/T]gatacgcttggttca | 5336 |
| rs9931137 | snp | A/G | 0.438806 | 0.163867 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926684 | CAGAAAGCCTCCACC[A/G]TCAGTGGTAGAGCTG | 5336 |
| rs9931756 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896577 | AGCGAGACCCTGTCT[C/G]AAAGGAAAAAAACCC | 5336 |
| rs9932049 | snp | C/T | 0.202959 | 0.245534 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961948 | agggcgatctggctg[C/T]gacatctgtcacccc | 5336 |
| rs9932181 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PLCG2 | GRCh38.p7 | 16:81912247 | ctattttatttttta[C/T]agagatgggggtctc | 5336 |
| rs9932209 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918433 | TGCTATTATTTCTAT[A/G]TAGGAATTTATTTCA | 5336 |
| rs9932299 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PLCG2 | GRCh38.p7 | 16:81918530 | cctggtgtgttctag[A/G]catctttattgaaga | 5336 |
| rs9932398 | snp | A/G | 0.197703 | 0.244469 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884831 | CAAAAGCAGACAGAC[A/G]GTTTAATGAACCACC | 5336 |
| rs9932427 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827088 | GGCCTAGGGCTGCAT[C/G]TCCTTGTTGACCTTG | 5336 |
| rs9932555 | snp | C/T | 0.440884 | 0.161442 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897523 | gatcgattatttttT[C/T]TCTTTTTTTCttttc | 5336 |
| rs9932652 | snp | A/C | 0.408871 | 0.193029 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875623 | TTGCAGCAGACATCA[A/C]GCAGCGTATCAGGTC | 5336 |
| rs9932716 | snp | A/C | 0.401037 | 0.199218 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875660 | CAATACTGTAATTTA[A/C]TACCTGGCTACGTGA | 5336 |
| rs9932725 | snp | A/C | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875681 | GGCTACGTGACTGCT[A/C]CCCTGCTACCTCCTG | 5336 |
| rs9932871 | snp | A/G | 0.465158 | 0.127307 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943319 | CTCAGGAAATTTACA[A/G]TCCTGGTAGAAGGGG | 5336 |
| rs9933031 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81827104 | TCCTTGTTGACCTTG[C/T]GCTGAAATAAGACTC | 5336 |
| rs9933601 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870700 | TTCCTTTCAAAAGCC[A/G]TGACACTGAAACAAT | 5336 |
| rs9933977 | snp | C/T | 0.158962 | 0.232835 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887833 | TGGGATTTCAGGGCA[C/T]GGAGAGGAAAGCAAC | 5336 |
| rs9934030 | snp | A/G | 0.467439 | 0.123371 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806207 | TGGCTAGTGGCTACC[A/G]TATTGGATAGCACAG | 5336 |
| rs9934119 | snp | C/G | 0.0912534 | 0.193131 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910157 | gtgcagtggcgtgat[C/G]tcggctcactgcaac | 5336 |
| rs9934788 | snp | A/C | 0.121717 | 0.214577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949174 | GATGCCAAGGACCTA[A/C]TATGAAAGCATGTCC | 5336 |
| rs9935242 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876132 | cctggctcagatgat[C/T]ctcccacctcagcct | 5336 |
| rs9935951 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | PLCG2 | GRCh38.p7 | 16:81901032 | ttgctgggagcatga[A/T]gtgagggaaggcgtg | 5336 |
| rs9936371 | snp | G/T | 0 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81786011 | ACCACGGTCAATGTA[G/T]ATTCCCTTGCGGAAT | 5336 |
| rs9936650 | snp | A/C | 0.24134 | 0.24985 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880698 | TGCTTCTTGGGAATA[A/C]GACTGTGGAGGGAAT | 5336 |
| rs9937124 | snp | C/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810956 | AGGTTATGCACCTGA[C/G]AAGCAGCCCAGGGAA | 5336 |
| rs9937223 | snp | A/G | 0.216649 | 0.247765 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811086 | TGCACTTCCTGGAAT[A/G]ACCCTGAGGTGTTCA | 5336 |
| rs9937776 | snp | C/T | 0.210909 | 0.246925 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780918 | TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA | 5336 |
| rs9937779 | snp | C/T | 0.348794 | 0.229651 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811002 | TCTAACAGTGGCCTT[C/T]CTGGCCCTAGTGGCT | 5336 |
| rs9937840 | snp | A/G | 0.146985 | 0.227789 | intron-variant | PLCG2 | GRCh38.p7 | 16:81890132 | cgtctcaaaaggcca[A/G]tcttaggttaaacca | 5336 |
| rs9938104 | snp | C/T | 0.158962 | 0.232835 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811369 | GATGGTTTTGCACGT[C/T]GGGGTTCAGGACTCA | 5336 |
| rs9938212 | snp | A/C | 0.480618 | 0.0965156 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795452 | CCTAATTGCAGTAAC[A/C]AGTTATTTCTTCCTG | 5336 |
| rs9938232 | snp | C/T | 0.264084 | 0.249603 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953622 | TTTTAAGTGAAAACT[C/T]AGACTCAAAAGAAAT | 5336 |
| rs9938253 | snp | A/G | 0.093777 | 0.195178 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886906 | TTACAGGTATCTAGT[A/G]CAATACCCTACACCA | 5336 |
| rs9938365 | snp | A/G | 0.148996 | 0.228688 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887047 | TGCCTTTTGATAAAT[A/G]CAAAAACTTTGTAGG | 5336 |
| rs9938623 | snp | C/T | 0.465368 | 0.126951 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924568 | GAACCGCCAGGCCTT[C/T]TGACTCCAGAGCTTA | 5336 |
| rs9939843 | snp | C/G | 0.404035 | 0.196909 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875508 | AATGTAAAGCATATA[C/G]AAGTAGAGAGAATAG | 5336 |
| rs9940275 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PLCG2 | GRCh38.p7 | 16:81787487 | ccctccttggcctcc[A/C]aaagcattgggatta | 5336 |
| rs9940401 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899609 | aagtgtcctcaccat[C/G]tgttgactgccatgt | 5336 |
| rs9940420 | snp | C/T | 0.401747 | 0.198678 | intron-variant | PLCG2 | GRCh38.p7 | 16:81875463 | AGCCATGGAATACTT[C/T]TTAATTTTTGAATCC | 5336 |
| rs9940462 | snp | A/G | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825856 | GGTTCAAGTCTTAGG[A/G]AGACAGAGACAAGAT | 5336 |
| rs9940492 | snp | A/G | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81825942 | TAGAAATCAGATGGC[A/G]TTGGACCAGAGAAAT | 5336 |
| rs9940772 | snp | A/G | 0.447162 | 0.153712 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796143 | GGGAAGTGGTGAGCC[A/G]CTGGCACTGAGGACT | 5336 |
| rs9941266 | snp | A/C | 0.412917 | 0.189626 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790700 | ACAATCCCTGTGCAG[A/C]CCTGGGTAAAATACC | 5336 |
| rs9944338 | snp | A/G | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782146 | CTCCCAAAGTGCTGG[A/G]ATTACAGTCATAAGC | 5336 |
| rs9944351 | snp | G/T | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782154 | GTGCTGGAATTACAG[G/T]CATAAGCCACCGTGC | 5336 |
| rs9944386 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782086 | TTTCATCGTGTTAGC[C/T]AGGATGGTCTTGATC | 5336 |
| rs9944387 | snp | A/C | 0.499994 | 0.00179711 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782174 | AGCCACCGTGCCTGG[A/C]CCATTTTATGCCTTT | 5336 |
| rs10163388 | snp | A/G | 0.108402 | 0.206034 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928203 | GAAGGTTCTTGAGCC[A/G]GGCTTTAGTAGGCAA | 5336 |
| rs10459875 | snp | C/G | 0.28578 | 0.247426 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945490 | TTGGGTGGGAGTGAC[C/G]GTTCTGTTTCAGCCC | 5336 |
| rs10514519 | snp | A/G | 0.318415 | 0.240457 | intron-variant | PLCG2 | GRCh38.p7 | 16:81941460 | GATGGCACTTTGACA[A/G]AACCAAACTATGTCA | 5336 |
| rs10514520 | snp | A/T | 0.299411 | 0.245069 | intron-variant | PLCG2 | GRCh38.p7 | 16:81953853 | CTCAGGAAAGGTGAT[A/T]AAGGGTTGCAGTTAT | 5336 |
| rs10530802 | in-del | -/CCCGCCC | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781877 | CTTTCCCCCCCCCCC[-/CCCGCCC]GCCCCCGAGACGGAG | 5336 |
| rs10549962 | in-del | -/ATATATATAT | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81838779 | TTAAAGTAAAATTAA[-/ATATATATAT]ATATATATATATATA | 5336 |
| rs10555890 | in-del | -/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81785497 | TTTTCGTTTATTTCA[-/T]TTTTTTTTTTTTTTT | 5336 |
| rs10579049 | in-del | -/AA | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81853331 | GTGAGATTCTGTCTC[-/AA]AAAAAAAAAACAAAA | 5336 |
| rs10580524 | in-del | -/A | 0.309648 | 0.24278 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853331 | GTGAGATTCTGTCTC[-/A]AAAAAAAAAAACAAA | 5336 |
| rs10580537 | in-del | -/ATAT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81838805 | TATATATATATATAT[-/ATAT]GTAAATAACATAGAT | 5336 |
| rs10622560 | in-del | -/GT | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81782245 | GAGATACAAGAAAAA[-/GT]CCTTTAGAAGGACAT | 5336 |
| rs10652557 | in-del | -/AT | 0.491629 | 0.0641526 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900107 | TAAATGTATGCATGC[-/AT]ACACATGCAAATTAC | 5336 |
| rs10685528 | in-del | -/AT | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900113 | TATGCATGCACACAT[-/AT]GCAAATTACATATGT | 5336 |
| rs10686622 | in-del | -/TG | 0.37778 | 0.214877 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852016 | GCCTTTGCTCACCTC[-/TG]TGGACTTCGTTCTGT | 5336 |
| rs10706670 | in-del | -/A | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81858868 | AGCTTTTTGGGGATT[-/A]AATGACTATCATCAG | 5336 |
| rs10710027 | in-del | -/T | 0.482747 | 0.0912627 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897549 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 5336 |
| rs10871422 | snp | C/T | 0.429837 | 0.173662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863303 | gactagcagaatatt[C/T]gtccttttgtatctg | 5336 |
| rs10871423 | snp | A/T | 0.499958 | 0.00459246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867709 | TCCCTTTTCTTTTTT[A/T]TTTTTGGAGATGGAG | 5336 |
| rs11150411 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793395 | CCTCTTGCATCTTGT[C/G]CATTTGAAAGGCTTG | 5336 |
| rs11150413 | snp | A/G | 0.476487 | 0.105846 | intron-variant | PLCG2 | GRCh38.p7 | 16:81809268 | CTGCTAGCCTGTGGT[A/G]CAGGATAGGCTGGGA | 5336 |
| rs11150414 | snp | A/G | 0.449473 | 0.150701 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811040 | GTGGTCTAAGGCCAC[A/G]TTTAACCTGTGTACC | 5336 |
| rs11150415 | snp | A/G | 0.471863 | 0.115225 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828538 | CCACCGCACCCGGCC[A/G]AGAAGCGTCATTTTT | 5336 |
| rs11150416 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829988 | GTGGACCCATGAACG[A/G]GCAGTGCTGTCTTGC | 5336 |
| rs11150417 | snp | C/T | 0.392881 | 0.205147 | intron-variant | PLCG2 | GRCh38.p7 | 16:81848347 | ATGCCTGCAGCTCTT[C/T]CCTGGGGCAGGGCTG | 5336 |
| rs11150418 | snp | A/C | 0.471388 | 0.116136 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861068 | AAACCAAAACCAAAA[A/C]CAAACCCTACCATTT | 5336 |
| rs11150419 | snp | C/T | 0.306927 | 0.243432 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867738 | AGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGTGCA | 5336 |
| rs11150420 | snp | A/G | 0.487933 | 0.0767327 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867843 | GCTGGGACTACAGGC[A/G]CCTGCTACCATGCCT | 5336 |
| rs11150421 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868299 | TAGGCCTTGTTCCTT[C/T]CCACTTCCCCTCCCT | 5336 |
| rs11150422 | snp | C/G | 0.323671 | 0.238899 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882227 | CGGGGGTGGCTCGTG[C/G]TGGCCCAGTGAGGCC | 5336 |
| rs11150423 | snp | C/G | 0.31503 | 0.241394 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885460 | TGAGGCACTGTGCCC[C/G]GCCCACTTTGCCAGT | 5336 |
| rs11150424 | snp | A/G | 0.31014 | 0.242659 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885866 | TGTTGTAATCATCAT[A/G]CCTTCCTAGTGCCGG | 5336 |
| rs11150425 | snp | C/T | 0.174932 | 0.238463 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939837 | ATGCGGAGATTGTCT[C/T]ACCAGAAGGGGGCAG | 5336 |
| rs11150426 | snp | C/G | 0.495999 | 0.0445491 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952978 | aaccacctggaataa[C/G]gcaggttgaaatcac | 5336 |
| rs11150427 | snp | C/T | 0.382279 | 0.212137 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955288 | CTGAGTCCGTGTTTT[C/T]CTAAAAGTAAATGAC | 5336 |
| rs11305035 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820626 | GGAAACATTACCCAA[-/T]TTTTTTTTTTTTGAG | 5336 |
| rs11355840 | in-del | -/C | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81781879 | TTCCCCCCCCCCCCC[-/C]GCCCGCCCCCGAGAC | 5336 |
| rs11362228 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920755 | GCTCTCAGCGGGGTA[-/G]GGGGAAGGCACTGGT | 5336 |
| rs11401096 | in-del | -/A | 0.397633 | 0.201754 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846235 | GGCAGGGAGGACAAG[-/A]AGGACTGGCCTCCCT | 5336 |
| rs11415278 | in-del | -/G | 0.488846 | 0.0738428 | upstream-variant-2KB, downstream-variant-500B | PLCG2, LOC105369213 | GRCh38.p7 | 16:81777659 | GATCTTGTGAAGTCA[-/G]CAAACGAGTCCTATG | 5336 |
| rs11548654 | snp | C/G/T | 1.70516e-05 | 0.00291985 | missense, synonymous-codon | PLCG2 | GRCh38.p7 | 16:81908556 | CCTGGTTCGGGAGAG[C/G/T]GAGACCTTCCCCAAT | 5336 |
| rs11548655 | snp | A/G | | | missense | PLCG2 | GRCh38.p7 | 16:81931512 | TGAAAGCCCCTCAGG[A/G]AAAAAACCAGAAGTC | 5336 |
| rs11548656 | snp | A/G | 0.0494433 | 0.149255 | missense | PLCG2 | GRCh38.p7 | 16:81883307 | CTGCTGTTTACCTGC[A/G]TGACTTCCAGAGGTT | 5336 |
| rs11548657 | snp | A/G | 0.00975586 | 0.0691575 | missense | PLCG2 | GRCh38.p7 | 16:81908479 | AAGGTGGAGAAGAGG[A/G]CGAGTGCCGAGAAGT | 5336 |
| rs11639517 | snp | C/T | 0.264906 | 0.249555 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878476 | taCTAgctataactt[C/T]ttctatctttagaac | 5336 |
| rs11639666 | snp | A/G | 0.115438 | 0.210697 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942789 | TTAATTTCGAACCCC[A/G]TGTTCCTCCTCTGCA | 5336 |
| rs11639731 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925974 | TAAGATGTGGCTGCT[C/T]GGATGACTGTGGGGA | 5336 |
| rs11639811 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865954 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGGGCT | 5336 |
| rs11640294 | snp | C/T | 0.368529 | 0.220116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861140 | GCTCTTCAGTCCTTG[C/T]CTCATGTTAGCCTCA | 5336 |
| rs11640363 | snp | C/T | 0.432504 | 0.170857 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861306 | CTGTCAGCTCTCTTA[C/T]TTTGTTCCTGAAAAT | 5336 |
| rs11640429 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876376 | AGAACCAAATGGTTT[A/C]TACAGCCTAAGTACC | 5336 |
| rs11640476 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876539 | CCTTCTCTTGTCCAG[A/C]TGGTAACTTCTCCTG | 5336 |
| rs11640578 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81804241 | tttttggttatcacc[A/G]tcctagtggaggtga | 5336 |
| rs11640696 | snp | G/T | 0.486 | 0.0824865 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878856 | GGCTCTTGGCTTTCA[G/T]TTGTTCTTTTTCATT | 5336 |
| rs11641105 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910116 | ttgttgttgagatgg[A/G]gtctcgctctgtcgc | 5336 |
| rs11641484 | snp | A/G | 0.165289 | 0.235211 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907305 | TAAATTTCATCGGGG[A/G]AAAAAAAAAAGAAGT | 5336 |
| rs11641776 | snp | A/C | 0.25045 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907262 | AGCTAAGAACTTAAC[A/C]CTGGTACTTTACAAT | 5336 |
| rs11642139 | snp | C/T | 0.485392 | 0.0842056 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784107 | CTGTTTCCCCATGGG[C/T]AGAGAGCAGGTGTAA | 5336 |
| rs11642172 | snp | C/T | 0.459004 | 0.137176 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852253 | GTAGTCCTGGCCAAA[C/T]AAGTCCCAGGAGGAT | 5336 |
| rs11642412 | snp | C/G | 0.457154 | 0.139954 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860115 | agctgggaactacag[C/G]tgtgtttcaccatgc | 5336 |
| rs11642558 | snp | A/T | 0.221737 | 0.248397 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793185 | CCAGGGGTGTTGGAT[A/T]AGATGGTGCTGGGAT | 5336 |
| rs11642588 | snp | A/T | 0.212122 | 0.247114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81793274 | GAGGGAGCTTGTGGT[A/T]CTGTTGGGCATGTTG | 5336 |
| rs11643258 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925975 | AAGATGTGGCTGCTT[A/G]GATGACTGTGGGGAC | 5336 |
| rs11643356 | snp | C/G | 0.488726 | 0.0742286 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778237 | aattagccaagtgtg[C/G]tgtgcctctatagtc | 5336 |
| rs11643670 | snp | C/G | 0.488666 | 0.0744214 | upstream-variant-2KB | PLCG2 | GRCh38.p7 | 16:81778243 | ccaagtgtggtgtgc[C/G]tctatagtcccagct | 5336 |
| rs11643838 | snp | A/G | 0.474723 | 0.109542 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861162 | TTAGCCTCACGTGAG[A/G]CACCTTATTTTTTTG | 5336 |
| rs11643875 | snp | A/G | 0.431769 | 0.17164 | intron-variant | PLCG2 | GRCh38.p7 | 16:81861269 | TGTGTCATTATCCTA[A/G]TTAATATCCAATAAC | 5336 |
| rs11643895 | snp | A/T | 0.210301 | 0.246828 | intron-variant | PLCG2 | GRCh38.p7 | 16:81780651 | CAGTTCCTCTGGAAG[A/T]GGAAAAGCACAGACC | 5336 |
| rs11644053 | snp | A/G | 0.303438 | 0.244222 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847357 | tgagagcctaattac[A/G]aaggcatgattgatt | 5336 |
| rs11644436 | snp | C/T | 0.247053 | 0.249983 | intron-variant | PLCG2 | GRCh38.p7 | 16:81878673 | gcacgtcagccatca[C/T]ctccatgtgttgcga | 5336 |
| rs11644646 | snp | A/C | 0.103503 | 0.202807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81870391 | TCTGTCTGACTCCCA[A/C]TGCTTTACAAAATGA | 5336 |
| rs11644729 | snp | G/T | 0.0872718 | 0.189788 | intron-variant | PLCG2 | GRCh38.p7 | 16:81917362 | ctatgaacatgggag[G/T]gcagctttctctttg | 5336 |
| rs11645217 | snp | C/T | 0.41325 | 0.18934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81833733 | AGAGGTGGGAACTTA[C/T]AGCCAAGGTGAGGGT | 5336 |
| rs11645251 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867356 | CTCATATTCTTGACC[C/T]ACCCACCCCACTAAT | 5336 |
| rs11645253 | snp | C/T | 0.084728 | 0.187577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867359 | ATATTCTTGACCCAC[C/T]CACCCCACTAATTTC | 5336 |
| rs11645421 | snp | G/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939556 | TGGATGTGGCTCCCA[G/T]GCTCTCCTCCCCTTT | 5336 |
| rs11645637 | snp | A/G | 0.490007 | 0.0699769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852218 | AGCTTGGGAGCAGCC[A/G]TGGAGGGGAGGTTTT | 5336 |
| rs11646017 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81910131 | agtctcgctctgtcg[C/G]ccaggctggagtgca | 5336 |
| rs11646189 | snp | C/G | 0.375 | 0.216506 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867855 | ggcgcctgctaccat[C/G]cctggctaatttttt | 5336 |
| rs11646370 | snp | A/T | 0.349452 | 0.229367 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942923 | AAAAACAATTATTTT[A/T]TTTTTTTTTATACAA | 5336 |
| rs11646670 | snp | G/T | 0.224116 | 0.248656 | intron-variant | PLCG2 | GRCh38.p7 | 16:81893075 | TATGTTGGCCAGGCT[G/T]GTCTTGAACACCTGA | 5336 |
| rs11646679 | snp | C/G | 0.436692 | 0.166271 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923205 | AACCCTAACCCCAGC[C/G]CTAAACCCTAGCCCC | 5336 |
| rs11646832 | snp | C/G | 0.182933 | 0.240836 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952932 | ggatagaccctgcag[C/G]taccatcttaatcag | 5336 |
| rs11646976 | snp | A/G | 0.128976 | 0.218754 | intron-variant | PLCG2 | GRCh38.p7 | 16:81907107 | GTAAGAAACCTGCAC[A/G]GTGTACACATGTACC | 5336 |
| rs11646981 | snp | A/G | 0.493432 | 0.0569306 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886524 | CCTAAGGAAATAATG[A/G]CAGCATTTTTAATAG | 5336 |
| rs11647099 | snp | C/T | 0.467744 | 0.122832 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828355 | agtacacgccattct[C/T]ctgcctcagcctcct | 5336 |
| rs11647261 | snp | C/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81886510 | TCCCAGACACTTATC[C/T]TAAGGAAATAATGGC | 5336 |
| rs11647603 | snp | C/T | 0.26078 | 0.249767 | intron-variant | PLCG2 | GRCh38.p7 | 16:81801372 | AATATGTTTTGCAGG[C/T]CTTTACATAAAAGAC | 5336 |
| rs11647768 | snp | C/T | 0.286303 | 0.24735 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898581 | ATTTCTATTGAGTGA[C/T]GTGATTTCCTATTTA | 5336 |
| rs11648071 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860352 | AATGCTGCTGTGGAA[A/G]CCTTTGGGTCTATCT | 5336 |
| rs11648542 | snp | C/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81816799 | tagccacggtgccca[C/G]ccAGAAATTATGACT | 5336 |
| rs11648561 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824051 | ttcctttcctttcct[G/T]tcctgtcctgtcctg | 5336 |
| rs11648625 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925240 | TCTCTCTGATGGCAG[C/T]AGTGCTACCTAGGGG | 5336 |
| rs11648862 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81925895 | TGTCTCAAAAAAAAA[A/G]AAAAAAAAATCCAGA | 5336 |
| rs11649062 | snp | C/T | 0.384976 | 0.210431 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847331 | ctaagccctgtcatc[C/T]tgggtttttatgaga | 5336 |
| rs11649130 | snp | A/T | 0.48 | 0.0979796 | intron-variant | PLCG2 | GRCh38.p7 | 16:81860175 | attattattattatt[A/T]ttttttttttttgta | 5336 |
| rs11649360 | snp | A/C | 0.499996 | 0.00139776 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781872 | ATGTCCTTTCCCCCC[A/C]CCCCCCCGCCCGCCC | 5336 |
| rs11649448 | snp | A/C | 0.324145 | 0.238752 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782111 | ttgatctcctgacct[A/C]atgatccgcccacct | 5336 |
| rs11649462 | snp | A/T | 0.499035 | 0.0219437 | intron-variant | PLCG2 | GRCh38.p7 | 16:81826309 | ATCCTAGGCTCAGAG[A/T]TGGGGGAACCGAGAA | 5336 |
| rs11859107 | snp | A/C | 0.216649 | 0.247765 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909090 | ATGTCTCAGTGCATT[A/C]AAAGATACTTCTTGA | 5336 |
| rs11859176 | snp | G/T | 0.126984 | 0.217653 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905552 | GCGGCCACGCCCCTT[G/T]CAGCTGCTTCTTGGA | 5336 |
| rs11859219 | snp | C/T | 0.248755 | 0.249997 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808155 | tcttgggtgtacacc[C/T]aggagtggaattgct | 5336 |
| rs11859255 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | PLCG2 | GRCh38.p7 | 16:81903558 | ctggctggggtcaca[A/G]gttaacaaaatagct | 5336 |
| rs11860342 | snp | C/T | 0.219049 | 0.248077 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904162 | cCCATGCCTGTATCA[C/T]GCTGCCATTCACAAG | 5336 |
| rs11860765 | snp | A/G | 0.342358 | 0.232314 | intron-variant | PLCG2 | GRCh38.p7 | 16:81868266 | CCAGGGCAGCCTGGC[A/G]CACAGTAGGTGCTCA | 5336 |
| rs11860917 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915651 | ACCCTGAATAAGCTA[A/G]TAGACGATGATCCTA | 5336 |
| rs11861143 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916252 | AAATCGCTTAAAGCA[A/T]TATATTTTTTTTTTC | 5336 |
| rs11861147 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784294 | TGATTAATGCCTTCC[C/T]CAATGGCTGATTAAT | 5336 |
| rs11862076 | snp | C/T | 0.119281 | 0.213102 | intron-variant | PLCG2 | GRCh38.p7 | 16:81790475 | GGCCCTGGGTGGGGA[C/T]TGTCAGTGTCACCGC | 5336 |
| rs11862261 | snp | A/G | 0.446249 | 0.154875 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894187 | TAATCCCAGCACTTC[A/G]GGAGGCTGAAGTGGG | 5336 |
| rs11862662 | snp | A/C | 0.372189 | 0.218105 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942287 | GCATCAAAGTGTGTC[A/C]ATTCATCTGCAGAAT | 5336 |
| rs11862758 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882350 | CTGCTTGGTCCAGGG[A/T]AGTGTCTTTCACACT | 5336 |
| rs11863080 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900157 | AGAATATATAAAACC[A/G]ATATACTTTATAAAT | 5336 |
| rs11863115 | snp | A/C/T | 0.0711985 | 0.176439 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909098 | GTGCATTAAAAGATA[A/C/T]TTCTTGAGGGCGTGC | 5336 |
| rs11863149 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930514 | gcactttgggaggcc[A/C]aggtgagtggatcgc | 5336 |
| rs11863412 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | PLCG2 | GRCh38.p7 | 16:81934048 | CTGGGGTCCACAGAG[A/C]CCCCGAGGATTTGAA | 5336 |
| rs11863650 | snp | A/G | 0.45692 | 0.1403 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882558 | CTGTCTGGGTATTGG[A/G]TAGGCACACTCACAT | 5336 |
| rs11863870 | snp | C/T | 0.109108 | 0.206518 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899882 | tcagatattgattca[C/T]tgaggaaaatgttgt | 5336 |
| rs11864384 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927932 | GCCCTTGCTTCCTCT[C/G]TACTGAGTTGCCCTT | 5336 |
| rs11864533 | snp | A/T | 0.493247 | 0.0577133 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882645 | CGCTCCTACTCCTCT[A/T]TCTTTCCTCCCCTCC | 5336 |
| rs11864701 | snp | A/G | 0.136506 | 0.222754 | intron-variant | PLCG2 | GRCh38.p7 | 16:81915680 | TAATGCTCCCCATGC[A/G]ACGGGTTGTGGATCC | 5336 |
| rs11864728 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81892899 | gttgcccaggctgga[G/T]tgcattggtgcgatc | 5336 |
| rs11864983 | snp | A/G | 0.115438 | 0.210697 | intron-variant | PLCG2 | GRCh38.p7 | 16:81789102 | ctgcatgctcttcac[A/G]tgtatcccggaactt | 5336 |
| rs11865090 | snp | C/T | 0.104504 | 0.2033 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916173 | TATTTAATAAAATAT[C/T]ACTGGAAATAAACCA | 5336 |
| rs11865395 | snp | C/T | 0.429785 | 0.173717 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880978 | CTCTTGTGTGTCGTT[C/T]GGGGCGGCTGTGCCG | 5336 |
| rs11866195 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PLCG2 | GRCh38.p7 | 16:81784302 | GCCTTCCCCAATGGC[C/T]GATTAATGCTAACTG | 5336 |
| rs11866355 | snp | A/G | 0.40853 | 0.193309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81807848 | aggagcaagagagag[A/G]gggagggaggtgcca | 5336 |
| rs11866488 | snp | A/G | 0.123452 | 0.215605 | intron-variant | PLCG2 | GRCh38.p7 | 16:81808180 | attgctgggccatgc[A/G]gtaaccattcattta | 5336 |
| rs11866585 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926353 | GCGGAAAATAGCTCA[A/G]GAGATGGGCAGGTTG | 5336 |
| rs11866777 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781705 | AACTGTTGGAGGGGC[C/G]CTTACCACTCAAGTA | 5336 |
| rs12102309 | snp | C/T | 0.499325 | 0.0183582 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873441 | GAACATGTCATAGAA[C/T]AATGATGACAGTGTG | 5336 |
| rs12102535 | snp | C/G | 0.283684 | 0.24772 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864777 | GCtgccatccttaat[C/G]gtttggtgatggctg | 5336 |
| rs12102881 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866875 | CCTGCCCTGGCCCAG[C/T]TGTTCCTTGGACCAC | 5336 |
| rs12149470 | snp | G/T | 0.270621 | 0.249148 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961938 | ATCGGATGTGAGGGC[G/T]ATCTGGCTGCGACAT | 5336 |
| rs12149858 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935487 | TTGATGATGCTGTAC[A/G/T]TATTTTTTTCTTTGG | 5336 |
| rs12325079 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895065 | GTAAAGCTTGAAGCA[A/G]TCAGCTCCTGTGCCC | 5336 |
| rs12325308 | snp | C/G/T | 0.0319951 | 0.122379 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927054 | GCCACCTGGTGACAG[C/G/T]GCCCCCATGTCCTCT | 5336 |
| rs12325524 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937161 | CCAAACTGCCCTCCA[C/T]AGAGATCGTGGGCGG | 5336 |
| rs12325585 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895231 | TTTCAACAGGTAAAG[A/T]CAGAAAATAAAACAC | 5336 |
| rs12325609 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802181 | gcagtggcgctatct[C/T]ggctcactgcaagct | 5336 |
| rs12443578 | snp | C/T | 0.384593 | 0.210677 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857695 | CCACTCTCATTACTT[C/T]ATCTAAACCTAAATA | 5336 |
| rs12444401 | snp | C/G | 0.499937 | 0.0055907 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949019 | ATTCAGAGAATAGAC[C/G]TGATTTGTTGCATTA | 5336 |
| rs12444459 | snp | C/G | 0.450985 | 0.148678 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919162 | GCAGGTGGTGGGACA[C/G]ATTTGGCCTACTCTT | 5336 |
| rs12445050 | snp | C/T | 0.175897 | 0.238765 | intron-variant | PLCG2 | GRCh38.p7 | 16:81837364 | TTTGCCTTTTCCAAA[C/T]GAGTGGGCACCCTGC | 5336 |
| rs12445314 | snp | C/G | 0.426481 | 0.183681 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802345 | tctcgatctcctgac[C/G]tcgtgatccacccgc | 5336 |
| rs12445395 | snp | A/T | 0.275464 | 0.2487 | intron-variant | PLCG2 | GRCh38.p7 | 16:81810650 | AATTTCTTTCTTTTT[A/T]TTTTTTGCTGGTGAT | 5336 |
| rs12445489 | snp | A/C | 0.451234 | 0.14834 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928969 | GCCTGGCTGAAATGC[A/C]GCGTGGAGTTGGGAG | 5336 |
| rs12445580 | snp | A/G | 0.483041 | 0.0905082 | intron-variant | PLCG2 | GRCh38.p7 | 16:81869192 | CCTCAAGGTGACAGA[A/G]CTGGGTCTCCCTCTT | 5336 |
| rs12445597 | snp | C/T | 0.41141 | 0.19091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798081 | AGTGATCTGCCTGCA[C/T]TGGCCTCCCAAAGTG | 5336 |
| rs12445621 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820350 | ctccctgccccaggc[C/T]accccaacctacttt | 5336 |
| rs12446070 | snp | A/G | 0.40157 | 0.198813 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882054 | ACAACAGACTCCTGG[A/G]CCCTGAGTGTTTAGT | 5336 |
| rs12446127 | snp | C/G | 0.499218 | 0.0197529 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921184 | TCCATTTCTTTCTTT[C/G]TTTTTTTTTCCAGGA | 5336 |
| rs12446501 | snp | G/T | 0.440884 | 0.161442 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799530 | cctggcctcaagaga[G/T]cctcccatcttggcc | 5336 |
| rs12446549 | snp | C/T | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857435 | ctctggctactgtaa[C/T]gaaatgctgtagact | 5336 |
| rs12446576 | snp | A/G | 0.385359 | 0.210185 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857706 | ACTTCATCTAAACCT[A/G]AATACCTCACAAAGG | 5336 |
| rs12446596 | snp | C/T | 0.43978 | 0.162738 | intron-variant | PLCG2 | GRCh38.p7 | 16:81926760 | AATTCACAACCTCCC[C/T]GAAATAGGGGTGAAC | 5336 |
| rs12446621 | snp | A/G | 0.384593 | 0.210677 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857870 | GTGTTAAATGGGAAT[A/G]TAATAGTACTTCCCT | 5336 |
| rs12447177 | snp | A/T | 0.384401 | 0.210799 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857611 | ttcctcagggtgtgc[A/T]tggatagagagggag | 5336 |
| rs12447311 | snp | A/G | 0.398174 | 0.201356 | intron-variant | PLCG2 | GRCh38.p7 | 16:81800708 | tattTCCAACCCTCt[A/G]tgataggcagaataa | 5336 |
| rs12447670 | snp | C/T | 0.431325 | 0.172108 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797888 | CAGGCTGAAGTGCAG[C/T]GGCACAATTTCAGTT | 5336 |
| rs12447699 | snp | C/T | 0.423726 | 0.179776 | intron-variant | PLCG2 | GRCh38.p7 | 16:81798047 | TGTTGACCAGGCTGG[C/T]CTTGAACTTCTGACC | 5336 |
| rs12447917 | snp | A/G | 0.498632 | 0.0261223 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871899 | tggtctatccatatt[A/G]tgtgacattatgcag | 5336 |
| rs12448055 | snp | C/T | 0.449218 | 0.151037 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919219 | AGTCAAGTCCTGTAG[C/T]TGGGGAGGAGAGGAA | 5336 |
| rs12448088 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929016 | CAGCTCTGCCTCTCT[C/G]TCGCTGTGAGACTAC | 5336 |
| rs12448089 | snp | A/G | 0.427727 | 0.175821 | intron-variant | PLCG2 | GRCh38.p7 | 16:81929022 | TGCCTCTCTGTCGCT[A/G]TGAGACTACAGGCCT | 5336 |
| rs12448118 | snp | A/C | 0.487241 | 0.0788465 | intron-variant | PLCG2 | GRCh38.p7 | 16:81865448 | CCCAAAGAAGCTCTC[A/C]GCCTCCAGTGTTTAC | 5336 |
| rs12448130 | snp | C/T | 0.00613496 | 0.055044 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919476 | ACCCTGTGTTCTTCC[C/T]GCTCCAGGGCTAGGG | 5336 |
| rs12448152 | snp | A/G | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81919763 | GAGTATTCACCATGT[A/G]TCTGATACTGCTGTA | 5336 |
| rs12448334 | snp | A/G | 0.491263 | 0.0655142 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795414 | AGGGCATAGCAACAA[A/G]GCTTTCCTATTAGTG | 5336 |
| rs12448393 | snp | G/T | 0.497473 | 0.0354532 | intron-variant | PLCG2 | GRCh38.p7 | 16:81829270 | CACACCAACGTGCCC[G/T]GCTAATTTTTGTATT | 5336 |
| rs12596249 | snp | A/G | 0.491368 | 0.0651254 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921762 | GGCAGAGGAAGAACC[A/G]CAGCGAATTTTCTGT | 5336 |
| rs12596299 | snp | G/T | 0.482083 | 0.0929373 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938678 | GGCTTTTCCAGTGAA[G/T]CTAGGAAAATTAGGG | 5336 |
| rs12596494 | snp | A/G | 0.366679 | 0.221102 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845023 | AGCCTCAAACTCCTG[A/G]GCTCAAGCAATTCTC | 5336 |
| rs12596533 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | PLCG2 | GRCh38.p7 | 16:81822338 | gtcctgctccccgga[A/G]cctgtgggtatgtca | 5336 |
| rs12596639 | snp | C/T | 0.203882 | 0.245709 | intron-variant | PLCG2 | GRCh38.p7 | 16:81859308 | ATGCCATGTTGGGTC[C/T]TGGGGTTGAGGATGA | 5336 |
| rs12596690 | snp | A/T | 0.144969 | 0.226867 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921634 | GCAGTGCAAATGCTA[A/T]CTCATATTCCCACCC | 5336 |
| rs12596760 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877442 | cctgggcgacacagc[A/G]agactccgtctcaaa | 5336 |
| rs12596817 | snp | A/C | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81914390 | AGGATGGCCCCCTCC[A/C]TGAGCCAGGTGGCAT | 5336 |
| rs12596830 | snp | C/G | 0.140242 | 0.224618 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924786 | CTGTTTGGCCTCCTT[C/G]CTGACATTGCTGTTC | 5336 |
| rs12597078 | snp | A/G | 0.406641 | 0.194842 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845613 | ATTTGCAGCCCCTGC[A/G]CTAGAATCTTGTTCC | 5336 |
| rs12598147 | snp | A/G | 0.126909 | 0.217598 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81961572 | ggctaaaattttgag[A/G]gagaagtggtatgaa | 5336 |
| rs12598194 | snp | C/T | 0.272241 | 0.249009 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791449 | GGCAATTCTTCTACT[C/T]TTTGTAGCCTGGACT | 5336 |
| rs12598402 | snp | C/T | 0.428182 | 0.17536 | intron-variant | PLCG2 | GRCh38.p7 | 16:81935243 | GCTGCTGGCATTCCT[C/T]GGCCTTCTCCTCTTC | 5336 |
| rs12598613 | snp | C/T | 0.2776 | 0.248472 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892365 | GGATACAGGATGTTG[C/T]GCTGATGTTCCAGTA | 5336 |
| rs12598645 | snp | G/T | 0.127599 | 0.217986 | intron-variant | PLCG2 | GRCh38.p7 | 16:81805366 | tagccgggtgtggtg[G/T]cgggtgcctatagtc | 5336 |
| rs12598676 | snp | C/T | 0.249886 | 0.25 | intron-variant | PLCG2 | GRCh38.p7 | 16:81791689 | CCCACCTCAGCCCCC[C/T]GAGTAGCTGGGATTA | 5336 |
| rs12598745 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PLCG2 | GRCh38.p7 | 16:81792103 | GCAGCCAAGCTCCCA[C/T]ATGAGCATGTCGACT | 5336 |
| rs12599032 | snp | C/G | 0.471673 | 0.115589 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828029 | TGGGAGGCGGAGCTT[C/G]CACTGAGCCGAGATC | 5336 |
| rs12599254 | snp | A/G | 0.00930212 | 0.0675613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81924597 | tacactcttaactcc[A/G]ttcatctgctaAGTC | 5336 |
| rs12599264 | snp | G/T | 0.497558 | 0.0348586 | intron-variant | PLCG2 | GRCh38.p7 | 16:81806517 | TCTTGGGGGTTGCTT[G/T]TGACCCAGGCAGCAC | 5336 |
| rs12599272 | snp | A/T | 0.184838 | 0.241358 | intron-variant | PLCG2 | GRCh38.p7 | 16:81844118 | agtagctgggactac[A/T]ggtgcccgccaccac | 5336 |
| rs12599660 | snp | C/G | 0.431473 | 0.171952 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841526 | GATTACAGGCATGAA[C/G]CACTGCGCCCGGCTG | 5336 |
| rs12600081 | snp | G/T | 0.154993 | 0.231244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842194 | AGAACTCCCTACAAA[G/T]GGAGGCTTTCTCCTC | 5336 |
| rs12600082 | snp | A/G | 0.154993 | 0.231244 | intron-variant | PLCG2 | GRCh38.p7 | 16:81842195 | GAACTCCCTACAAAG[A/G]GAGGCTTTCTCCTCT | 5336 |
| rs12600281 | snp | A/C | 0.495445 | 0.0475058 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835449 | aaaaatacaaaaatt[A/C]gccgggtgtggtgac | 5336 |
| rs12716920 | snp | A/G | 0.107341 | 0.205301 | intron-variant | PLCG2 | GRCh38.p7 | 16:81788747 | CTGGTTTTGGAGCCC[A/G]GTGGGTCTCTTGTGG | 5336 |
| rs12716921 | snp | A/T | 0.499631 | 0.0135733 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873038 | GGGAAAACATATTTC[A/T]TAGAGTGGATCATTG | 5336 |
| rs12716922 | snp | A/C | 0.499703 | 0.0121769 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873161 | ACTGGATTCTAGACC[A/C]ACTTGACCTCTAACT | 5336 |
| rs12716923 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925811 | AGAATTGCTTGAACC[C/T]GGGAGGCGAAGGTTG | 5336 |
| rs12716924 | snp | C/G | 0.426201 | 0.177351 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927415 | GGCTTGGAAGGATTT[C/G]ATTATGCAGGAGAAT | 5336 |
| rs12716925 | snp | A/T | 0.426201 | 0.177351 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927417 | CTTGGAAGGATTTCA[A/T]TATGCAGGAGAATTC | 5336 |
| rs12716926 | snp | A/G | 0.424503 | 0.179021 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927655 | CACTTTCAGCGTGCT[A/G]GCACTCCACCAAGGA | 5336 |
| rs12716927 | snp | C/T | 0.439224 | 0.163383 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927660 | TCAGCGTGCTAGCAC[C/T]CCACCAAGGATGATA | 5336 |
| rs12716928 | snp | A/G | 0.170408 | 0.236992 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945447 | AAGATACTGTTAACC[A/G]TGGTTCCTTTTAGGA | 5336 |
| rs12917731 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81835357 | tcccagcactttggg[A/T]ggccaaagcgggcag | 5336 |
| rs12917936 | snp | G/T | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856976 | GCTGGGAAAGGTGAG[G/T]AAACAGATTCTTCCC | 5336 |
| rs12917955 | snp | C/T | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857011 | gctttcagaaggaat[C/T]cagagatctcatgca | 5336 |
| rs12918090 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81805528 | aaaaaacaaaaCGCA[A/G]GAAAACAAcaaaaaa | 5336 |
| rs12918182 | snp | A/T | 0.396182 | 0.202807 | intron-variant | PLCG2 | GRCh38.p7 | 16:81799382 | TTCATTTTGTACTAC[A/T]TTGTGACCATGTTAG | 5336 |
| rs12918369 | snp | A/G | 0.479421 | 0.0993283 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939297 | TCAGCCTAACCTGGG[A/G]GATCTTAGCCCCTAG | 5336 |
| rs12918486 | snp | A/T | 0.499933 | 0.00579035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873021 | CTATCTGCCCAGATT[A/T]GGGGAAAACATATTT | 5336 |
| rs12918716 | snp | A/T | 0.358303 | 0.225323 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846691 | aatattttcaagata[A/T]cagttcttcctggct | 5336 |
| rs12919270 | snp | C/T | 0.379158 | 0.214052 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847642 | tggattctgcgtctg[C/T]ggatttaagctatgg | 5336 |
| rs12920068 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841553 | gctGTAAACTTTACT[G/T]TTTGCAAAGTTTTTT | 5336 |
| rs12920079 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803620 | ttttcttttcttttc[C/T]tttcttttcttcttc | 5336 |
| rs12921234 | snp | A/G | 0.476401 | 0.106032 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884645 | catgtCTTTTCACAT[A/G]TAAATCTCAAATTTT | 5336 |
| rs12921605 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | PLCG2 | GRCh38.p7 | 16:81952281 | TATATATATATTCAC[A/G]CGTAGATGAATAAAT | 5336 |
| rs12921746 | snp | C/T | 0.474091 | 0.11083 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885272 | caggtgatccacccg[C/T]cttggcctcccaaag | 5336 |
| rs12921764 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PLCG2 | GRCh38.p7 | 16:81885309 | gattacaggtgtgag[A/C]caccacgcccagccc | 5336 |
| rs12921780 | snp | C/T | 0.343477 | 0.231866 | intron-variant | PLCG2 | GRCh38.p7 | 16:81945520 | CTGTGTTCTTTTATA[C/T]TAAAACAAGCCAGCA | 5336 |
| rs12921791 | snp | G/T | 0.49681 | 0.0398085 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852436 | ATCCCATGAAAAGAT[G/T]ATTGTTGTTGTAGTT | 5336 |
| rs12921938 | snp | C/G | 0.489665 | 0.0711382 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852473 | AAGAAAGGGAAAGAA[C/G]GGACTGGTTGAGCTT | 5336 |
| rs12922252 | snp | C/G | 0.34659 | 0.230587 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855489 | GGGACATTTACTTTT[C/G]GGTCAAATAACTTAT | 5336 |
| rs12922444 | snp | C/G | 0.289942 | 0.246789 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852105 | TTCTCACTCTCATCT[C/G]CAGGAGTGCTGGAGT | 5336 |
| rs12923110 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852157 | ATAACACTTTCTTCC[A/G]TGGTAGACAAGGTGG | 5336 |
| rs12923387 | snp | A/T | 0.312837 | 0.241974 | intron-variant | PLCG2 | GRCh38.p7 | 16:81940200 | GGTGGCTTGGAGAGC[A/T]GGTGTACAGCCTGTC | 5336 |
| rs12923488 | snp | A/T | 0.495745 | 0.0459295 | intron-variant | PLCG2 | GRCh38.p7 | 16:81852448 | GATGATTGTTGTTGT[A/T]GTTTTTCAGAAGAAA | 5336 |
| rs12923507 | snp | G/T | 0.483126 | 0.0902898 | intron-variant | PLCG2 | GRCh38.p7 | 16:81867946 | CCTCGTGATCCGCCC[G/T]CCTCAGCCTCCCAAA | 5336 |
| rs12923776 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | PLCG2 | GRCh38.p7 | 16:81818757 | CCATGGAAACTGAGG[C/G]CTGCTGAGCCTGTCA | 5336 |
| rs12923859 | snp | A/G | 0.423881 | 0.179625 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880298 | CCAGTGGAGGTGCCT[A/G]TCTCAACTGTTTTGA | 5336 |
| rs12924097 | snp | C/G | 0.482757 | 0.0912364 | intron-variant | PLCG2 | GRCh38.p7 | 16:81898357 | GGTTCAGATTTTGCT[C/G]TCAGTTACATTTTGA | 5336 |
| rs12924530 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81803587 | ctttcctttcctttc[C/T]tttcttttctccttt | 5336 |
| rs12924579 | snp | A/T | 0.499996 | 0.00139776 | intron-variant | PLCG2 | GRCh38.p7 | 16:81913139 | CCCAACTGCAGCTGC[A/T]GCCCAACCACCTCTA | 5336 |
| rs12924928 | snp | C/G | 0.488466 | 0.0952725 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884503 | cacagccaccgacag[C/G]tggtttacccttttt | 5336 |
| rs12925104 | snp | C/G | 0.437824 | 0.164991 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944136 | AAGTAATACTGAGCT[C/G]TGGGTGGTGAGATGC | 5336 |
| rs12925139 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PLCG2 | GRCh38.p7 | 16:81876699 | GCTGTTTCTCCTGAC[C/T]TCACTGGCCCTTTGC | 5336 |
| rs12926118 | snp | C/G | 0.338069 | 0.233974 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855652 | AGACAGATGTGTGTA[C/G]TGGGATAAGACCTAG | 5336 |
| rs12926234 | snp | C/G | 0.358303 | 0.225323 | intron-variant | PLCG2 | GRCh38.p7 | 16:81845668 | TGAATGCACTGCGTT[C/G]AGCGCAGTGGGCCTG | 5336 |
| rs12926653 | snp | A/G | 0.185472 | 0.241529 | intron-variant | PLCG2 | GRCh38.p7 | 16:81853194 | aaactagccgggcat[A/G]gtggcacatgcctgt | 5336 |
| rs12927160 | snp | A/G/T | 0.499853 | 0.008585 | intron-variant | PLCG2 | GRCh38.p7 | 16:81910020 | tggggtggggtgggg[A/G/T]ggggGAAGTAGGTAG | 5336 |
| rs12927930 | snp | C/T | 0.240478 | 0.249819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81880395 | TCTAGGACTCTACTC[C/T]GTAGAAAAACTGGCA | 5336 |
| rs12928126 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949692 | TTTGCAGTACAGTTA[C/G]ATCTTACAGGATGAT | 5336 |
| rs12930443 | snp | G/T | 0.384785 | 0.210554 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856894 | CCCAGAGAAAGAGAT[G/T]TGAGGATGGAAACAA | 5336 |
| rs12930505 | snp | C/T | 0.338976 | 0.23363 | intron-variant | PLCG2 | GRCh38.p7 | 16:81855650 | GGAGACAGATGTGTG[C/T]ACTGGGATAAGACCT | 5336 |
| rs12930646 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81923247 | CCTAACCCCTAACCC[C/T]TAACCCCAACCCAGG | 5336 |
| rs12930760 | snp | C/G | 0.385168 | 0.210309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857135 | gcagaggagactgat[C/G]ACTGAACCTTTGATA | 5336 |
| rs12930890 | snp | A/G | 0.138207 | 0.223612 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857193 | CCTGTTGATGTCTCC[A/G]TCATCCCTCTCTTCT | 5336 |
| rs12931199 | snp | C/T | 0.380138 | 0.213458 | intron-variant | PLCG2 | GRCh38.p7 | 16:81856706 | GGAAGCTGAATACTG[C/T]CCTCCCACGATGCCC | 5336 |
| rs12931309 | snp | C/G | 0.4944 | 0.0526182 | intron-variant | PLCG2 | GRCh38.p7 | 16:81894120 | TGGATTGGGGGGTCT[C/G]TGAGCAAATGTGAAA | 5336 |
| rs12931658 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896237 | TCAGAACCCCCGAAA[A/G]AGAGGGAAAggctgg | 5336 |
| rs12931725 | snp | C/T | 0.385168 | 0.210309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857046 | gtctattttagactt[C/T]tggcctctctaacag | 5336 |
| rs12931737 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81863945 | CCTATTTGAGACTCC[A/T]GAATGTTAGAGTCAC | 5336 |
| rs12932057 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896485 | TGGGAAGCTGAGGTG[A/G]GAGGATTGCTTGAAC | 5336 |
| rs12932333 | snp | A/G | 0.385168 | 0.210309 | intron-variant | PLCG2 | GRCh38.p7 | 16:81857077 | tctgaaaataaatct[A/G]tattactttaagtca | 5336 |
| rs12932436 | snp | C/T | 0.383053 | 0.211653 | intron-variant | PLCG2 | GRCh38.p7 | 16:81823928 | ttccatcctttcttc[C/T]ttccttcctcccttc | 5336 |
| rs12932636 | snp | C/G | 0.17461 | 0.238362 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846859 | tctctttcctcttcc[C/G]tctgtactcaacact | 5336 |
| rs12932761 | snp | C/T | 0.135825 | 0.222405 | intron-variant | PLCG2 | GRCh38.p7 | 16:81854215 | AGCGGAAACCCCAAA[C/T]TCTTCAGACTCCAGG | 5336 |
| rs12932808 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896293 | cggcactttgggagg[C/G/T]tgaggtgtgatcact | 5336 |
| rs12932861 | snp | C/T | 0.116488 | 0.211364 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950002 | TAACCACTGTCAGAA[C/T]TGAAAAACAGACAAG | 5336 |
| rs12932903 | snp | A/G | 0.359787 | 0.224604 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846709 | gttcttcctggcttc[A/G]tctatagattcaaca | 5336 |
| rs12932964 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81896356 | atggtgaaacccctt[C/T]tctaccaaaacacac | 5336 |
| rs12933001 | snp | A/T | 0.430583 | 0.172886 | intron-variant | PLCG2 | GRCh38.p7 | 16:81794806 | GTAGAAAGGATGGGA[A/T]AAATACTACATTTTC | 5336 |
| rs12933012 | snp | C/G | 0.181659 | 0.240478 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847121 | ttccaataacccact[C/G]cttggatttgattaa | 5336 |
| rs12933067 | snp | C/T | 0 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81802094 | CAGGTGAGTACAGTC[C/T]TTTTTTTtttttttt | 5336 |
| rs12933078 | snp | C/G | 0.404907 | 0.196224 | intron-variant | PLCG2 | GRCh38.p7 | 16:81904916 | ttactgggacagagt[C/G]tcactctgttgccca | 5336 |
| rs12933299 | snp | A/G | 0.457969 | 0.138741 | intron-variant | PLCG2 | GRCh38.p7 | 16:81803477 | ttgatggacatttag[A/G]tagttctctcttttt | 5336 |
| rs12933303 | snp | C/G | 0.109108 | 0.206518 | intron-variant | PLCG2 | GRCh38.p7 | 16:81834767 | GGGCTCCCAGGACGA[C/G]GACAATCTCCTTTAA | 5336 |
| rs12933380 | snp | A/G | 0.361617 | 0.225138 | intron-variant | PLCG2 | GRCh38.p7 | 16:81846976 | TTCAATTCTGATACT[A/G]TCTACTTGGAGCTAG | 5336 |
| rs12933526 | snp | A/T | 0.353154 | 0.227726 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847055 | TTTCAGGTGCCAGTC[A/T]CAAGCCCAAGTTGTG | 5336 |
| rs12933559 | snp | A/G | 0.444799 | 0.156695 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847127 | taacccactccttgg[A/G]tttgattaatttgct | 5336 |
| rs12933648 | snp | C/G | 0.379942 | 0.213577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81847547 | agatacttatcactg[C/G]agattccaagggtgt | 5336 |
| rs12933680 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | PLCG2 | GRCh38.p7 | 16:81896457 | GTGGCATGTGCCTGT[A/G]GTCCCAGTTACTTGG | 5336 |
| rs12933962 | snp | A/G | 0.114387 | 0.210022 | intron-variant | PLCG2 | GRCh38.p7 | 16:81820763 | gtagctgggattaca[A/G]gtgcacaccatcatg | 5336 |
| rs12934301 | snp | G/T | 0.190519 | 0.242821 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851057 | TGGGGTGTGACGGGG[G/T]ATGAGTCCTTTCTCT | 5336 |
| rs12934353 | snp | C/G | 0.489376 | 0.0721049 | intron-variant | PLCG2 | GRCh38.p7 | 16:81782464 | TGGTGCTCTCTCCTG[C/G]GCTCAAGGTCTTGGA | 5336 |
| rs12934982 | snp | C/T | 0.372592 | 0.217879 | intron-variant | PLCG2 | GRCh38.p7 | 16:81900109 | AAATGTATGCATGCA[C/T]ACATGCAAATTACAT | 5336 |
| rs12934992 | snp | A/G | 0.212122 | 0.247114 | intron-variant | PLCG2 | GRCh38.p7 | 16:81851534 | gttgttgttgttgag[A/G]cgaagtctcactctg | 5336 |
| rs13330054 | snp | G/T | 0.484209 | 0.0874434 | intron-variant | PLCG2 | GRCh38.p7 | 16:81873290 | TACTCTTTAATCCCC[G/T]CTCCTTTAGACAGGA | 5336 |
| rs13330258 | snp | A/C | 0.308661 | 0.24302 | intron-variant | PLCG2 | GRCh38.p7 | 16:81882713 | TCCTTGCCAGGTACT[A/C]TCTGCACCTCCTTCT | 5336 |
| rs13330508 | snp | A/G | 0.0861826 | 0.188849 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962369 | ATTATACAGAATTAG[A/G]AAATTGGCATTTAAA | 5336 |
| rs13331425 | snp | C/T | 0.296109 | 0.245711 | intron-variant | PLCG2 | GRCh38.p7 | 16:81954775 | TCCATGTCTTTGCTG[C/T]TGTACATGGTGCTGC | 5336 |
| rs13331678 | snp | C/T | 0.130694 | 0.219696 | intron-variant | PLCG2 | GRCh38.p7 | 16:81921693 | AGGGATGGATTTTAC[C/T]TTCAGCCCTCGGCTC | 5336 |
| rs13331697 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | PLCG2 | GRCh38.p7 | 16:81877235 | caaggcgggcggatc[A/G]cgaggtcaggagatc | 5336 |
| rs13331991 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884416 | AAGAAGTATTCAGCA[C/G]CAAGTACCTACAGTG | 5336 |
| rs13333255 | snp | A/G | 0.280256 | 0.248162 | intron-variant | PLCG2 | GRCh38.p7 | 16:81899272 | GAGGAGtatgtgtgt[A/G]tatatatatatatat | 5336 |
| rs13333348 | snp | A/G | 0.0970459 | 0.19775 | intron-variant | PLCG2 | GRCh38.p7 | 16:81895774 | TGTCAGTGAACACAC[A/G]TGGTATTGAGGCTGC | 5336 |
| rs13333420 | snp | A/T | 0.493432 | 0.0569306 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923781 | GAAAATGGATAAACA[A/T]CAATATTAACAGGTA | 5336 |
| rs13333641 | snp | C/T | 0.0146672 | 0.084371 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960730 | CATGTTCTAATACTT[C/T]GTATGCTTTGTGACC | 5336 |
| rs13333713 | snp | C/T | 0.00130739 | 0.0255341 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895886 | GATCAAGTTTGACGA[C/T]GTCGTGCAGGCCATC | 5336 |
| rs13333716 | snp | C/G | 0.0981236 | 0.198579 | synonymous-codon | PLCG2 | GRCh38.p7 | 16:81895922 | CCACGCCTTTGTTAC[C/G]TCGAGGTCAGTTGGC | 5336 |
| rs13334290 | snp | C/T | 0.240478 | 0.249819 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841389 | AGGCACCCAGGCGCT[C/T]ACTACCATGCCCAGC | 5336 |
| rs13334419 | snp | A/G | 0.356169 | 0.226336 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841878 | GGGTCCTTGGCTGAG[A/G]TCAGTAAGCAACGCT | 5336 |
| rs13334467 | snp | C/G | 0.039522 | 0.134904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81850823 | agtattataatgcag[C/G]caaggtggaggactg | 5336 |
| rs13334750 | snp | A/T | 0.407158 | 0.194426 | intron-variant | PLCG2 | GRCh38.p7 | 16:81864190 | GGCTGATTGAGTAGG[A/T]GGTGGGCAGGGCTCA | 5336 |
| rs13334875 | snp | A/T | 0.14933 | 0.228835 | intron-variant | PLCG2 | GRCh38.p7 | 16:81887290 | acgcccagctaattt[A/T]ttgtgtttttagtag | 5336 |
| rs13334984 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874414 | TAAAAATTTAATTTA[A/G]TGACAGATTTGAATA | 5336 |
| rs13335020 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874544 | TTACTTCCTGTTCCT[A/G]GCTGGAAGCACAGGG | 5336 |
| rs13335046 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824046 | ttcctttcctttcct[G/T]tcctgtcctgtcctg | 5336 |
| rs13335168 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824294 | atgcgtcaccacacc[C/T]ggctaatttgtgtat | 5336 |
| rs13335344 | snp | C/T | 0.231482 | 0.249313 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841552 | GGCTGTAAACTTTAC[C/T]TTTTGCAAAGTTTTT | 5336 |
| rs13335473 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81944725 | aagtgatcctcctgc[A/C]ttgccctccccaagt | 5336 |
| rs13336519 | snp | G/T | 0.242775 | 0.249896 | intron-variant | PLCG2 | GRCh38.p7 | 16:81905864 | gggatttagtcgtgt[G/T]gcccagggtgatttc | 5336 |
| rs13337013 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | PLCG2 | GRCh38.p7 | 16:81884419 | AAGTATTCAGCACCA[A/G]GTACCTACAGTGCTG | 5336 |
| rs13337974 | snp | G/T | 0.498693 | 0.0255257 | intron-variant | PLCG2 | GRCh38.p7 | 16:81916591 | AACCATTTTTTTTTT[G/T]TGTGTGGTGAGACTT | 5336 |
| rs13338037 | snp | C/G | 0.229723 | 0.249176 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841381 | GGGATTACAGGCACC[C/G]AGGCGCTTACTACCA | 5336 |
| rs13338629 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824354 | ggccaggctggtctt[A/G]aactcctgatcttaa | 5336 |
| rs13338981 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PLCG2 | GRCh38.p7 | 16:81811910 | ttgctggatcaaatg[A/G]tatttctggtgctag | 5336 |
| rs13339067 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PLCG2 | GRCh38.p7 | 16:81832743 | TCTGTGAGTGGTATG[A/G]TATCCAGTTGACTGC | 5336 |
| rs13339274 | snp | C/T | 0.215144 | 0.247558 | intron-variant | PLCG2 | GRCh38.p7 | 16:81841954 | TGTTGCAAGGTGGTA[C/T]AGAAAACCATTCAGC | 5336 |
| rs13380692 | snp | A/G | 0.454904 | 0.143228 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797746 | CTTTAACCATACACC[A/G]TGGTTCCACTCGTGG | 5336 |
| rs13380701 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | PLCG2 | GRCh38.p7 | 16:81797646 | AAGGCCCTGGCTGCC[A/C]CTTTCAGCCTCGGAC | 5336 |
| rs16955980 | snp | G/T | 0.490908 | 0.0689722 | intron-variant | PLCG2 | GRCh38.p7 | 16:81923698 | CCCCCTTTGTCATCC[G/T]GGGCTGGCTTTGACC | 5336 |
| rs16955993 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | PLCG2 | GRCh38.p7 | 16:81927469 | AATGGGGAATTTGTC[C/G]TTTGCTTAAGCAACT | 5336 |
| rs16955997 | snp | G/T | 0.039522 | 0.134904 | intron-variant | PLCG2 | GRCh38.p7 | 16:81928347 | ATTGGAAAATGAAAC[G/T]CCGAACCTCCTGGCA | 5336 |
| rs16956005 | snp | A/T | 0.262435 | 0.249691 | intron-variant | PLCG2 | GRCh38.p7 | 16:81930855 | TGAAACAGTTCACAA[A/T]ATTTTATGTATTGTA | 5336 |
| rs16956011 | snp | A/G | 0.328382 | 0.237395 | intron-variant | PLCG2 | GRCh38.p7 | 16:81936748 | CAGAGACATTTACAT[A/G]CTGGCATAACTAACA | 5336 |
| rs16956018 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PLCG2 | GRCh38.p7 | 16:81937630 | CTTTGAGTGAGATAC[C/T]TATTTGAACAGCTGC | 5336 |
| rs16956020 | snp | A/G | 0.216649 | 0.247765 | intron-variant | PLCG2 | GRCh38.p7 | 16:81938663 | GCAGAAGGTTGCTCC[A/G]GCTTTTCCAGTGAAT | 5336 |
| rs16956026 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | PLCG2 | GRCh38.p7 | 16:81939793 | GCATATTTATTTACA[G/T]GGTTGCTAAGGGGAT | 5336 |
| rs16956034 | snp | G/T | 0.369346 | 0.219673 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942359 | AACCTCAAGGGAGAT[G/T]AAAAATGTGACCTTC | 5336 |
| rs16956040 | snp | C/T | 0.306679 | 0.24349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81942572 | TTAAACCAGTTGGAG[C/T]GCAGGAAGGAAAGCA | 5336 |
| rs16956064 | snp | C/T | 0.222035 | 0.248431 | intron-variant | PLCG2 | GRCh38.p7 | 16:81946523 | CGGTACTTGTAAGTT[C/T]CCCATAGTTTCACTT | 5336 |
| rs16956065 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | PLCG2 | GRCh38.p7 | 16:81947221 | ATGCAGATTTGACTT[C/T]CTTGATGAGGGAAGC | 5336 |
| rs16956070 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PLCG2 | GRCh38.p7 | 16:81948020 | TGCCTGTTTCATCAG[A/G]TATGGGTCCCTAATT | 5336 |
| rs16956082 | snp | A/T | 0.230603 | 0.249246 | intron-variant | PLCG2 | GRCh38.p7 | 16:81949889 | CTTTGACGACTAGGG[A/T]ATCAGTCAGTAAATA | 5336 |
| rs16956085 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PLCG2 | GRCh38.p7 | 16:81950306 | TCAATCTAGAATTTA[A/C]GATCAGAAGTACTAC | 5336 |
| rs16956096 | snp | A/G | 0.182614 | 0.240747 | intron-variant | PLCG2 | GRCh38.p7 | 16:81956296 | TTTAGTTCTCATGTC[A/G]TGCTGTTTTTTTCTC | 5336 |
| rs16956102 | snp | A/C | 0.0256215 | 0.110247 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81960123 | CCTTCTCCTGGTGCT[A/C]CAACCGGAATCCACC | 5336 |
| rs16956106 | snp | C/G | 0.121369 | 0.214369 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81962404 | CTCAATAATTTGTCC[C/G]TGGTTTTTAATTTTC | 5336 |
| rs17202240 | snp | C/G | 0.17654 | 0.238964 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925272 | CCGCCTGGGTGAAAC[C/G]GGCTTTTTTGCATAC | 5336 |
| rs17202296 | snp | C/G | 0.363776 | 0.222609 | intron-variant | PLCG2 | GRCh38.p7 | 16:81925586 | ACGGAGCACAGACTT[C/G]ATTAAGATCCAGAAA | 5336 |
| rs17203303 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943766 | AACTAGCAGCAAAAA[C/T]CACATTGTAGCGATA | 5336 |
| rs17203310 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PLCG2 | GRCh38.p7 | 16:81943767 | ACTAGCAACAAAAAT[C/T]ACATTGTAGCGATAG | 5336 |
| rs17793122 | snp | A/G | 0.396364 | 0.202676 | intron-variant | PLCG2 | GRCh38.p7 | 16:81955879 | ATTTATGATACCTTG[A/G]CTTTTTTGGGTAACA | 5336 |
| rs17793218 | snp | C/T | 0.0513262 | 0.151752 | utr-variant-3-prime | PLCG2 | GRCh38.p7 | 16:81959867 | AGGTGTTGCTGTCAT[C/T]ACCTCCTTTCAGCTC | 5336 |
| rs17856213 | snp | G/T | 0 | 0 | missense | PLCG2 | GRCh38.p7 | 16:81931562 | CCCAAGCAGCAGGGC[G/T]ATCCTCCGGTGGAGT | 5336 |
| rs28366533 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874830 | GAAATGTAATCTCAC[A/G]TTTGTGTCTCCCTGG | 5336 |
| rs28376278 | snp | A/G | 0.402806 | 0.197864 | intron-variant | PLCG2 | GRCh38.p7 | 16:81796844 | GGTCTCCAGAACTGT[A/G]AGACAAACTTCTGTT | 5336 |
| rs28380426 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824531 | GCCAGGTGTGGCTGG[C/G]ACTTTTCGTTGGGAT | 5336 |
| rs28394704 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81900072 | CCTTATAGAAATATA[C/T]ATATATACACATACA | 5336 |
| rs28405634 | snp | A/G | 0.472896 | 0.113214 | intron-variant | PLCG2 | GRCh38.p7 | 16:81795293 | CACTAGCCTAGCTGG[A/G]GAAGGCCTCAGGGTG | 5336 |
| rs28406173 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PLCG2 | GRCh38.p7 | 16:81824442 | CATGGCCCCAGCCAC[C/T]TATTTTCTTGTGATT | 5336 |
| rs28415183 | snp | C/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81866343 | ATGAGAGGACGCTGG[C/T]CTCTCCCTTGCTCCC | 5336 |
| rs28426998 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PLCG2 | GRCh38.p7 | 16:81874892 | AACAGTATCATTAAC[A/G]AAGATGATAGCCAAC | 5336 |
| rs28430364 | snp | G/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81824076 | GTCCTGTCCTGTCCT[G/T]TCCTGTCCTGTCCTG | 5336 |
| rs28446814 | snp | A/T | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81877972 | CCCTCTTTTTTTTTT[A/T]ATTTTTTTTTTTTTT | 5336 |
| rs28452625 | snp | A/G | 0.286825 | 0.247273 | intron-variant | PLCG2 | GRCh38.p7 | 16:81897410 | ATAGAGGTGATAACT[A/G]TGTGCACCTCACAGG | 5336 |
| rs28463426 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | PLCG2 | GRCh38.p7 | 16:81781906 | AGACGGAGTCTTGCT[C/G]TGTCGCCCAGGCTGG | 5336 |
| rs28464754 | snp | A/G | 0.48 | 0.0979796 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866251 | CTTTCTCCCAGGATG[A/G]GCTCCACTGGGGCAC | 5336 |
| rs28481521 | snp | C/T | 0.273318 | 0.24891 | intron-variant | PLCG2 | GRCh38.p7 | 16:81909584 | ACGACACCTGAATAA[C/T]TTTTAAATTTTTTGT | 5336 |
| rs28482417 | snp | C/T | 0.0285453 | 0.116008 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889296 | GGCTGGGCTTGTTGT[C/T]GCTTGGGGGTGACTT | 5336 |
| rs28489594 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PLCG2 | GRCh38.p7 | 16:81871235 | AAAAAGTGCAACTCA[A/C]TCTACTGCATTATTT | 5336 |
| rs28516048 | snp | A/G | | | intron-variant | PLCG2 | GRCh38.p7 | 16:81950081 | AAAATAATGTAAAGA[A/G]TCAGAATAAGTTAAA | 5336 |
| rs28520093 | snp | C/G | 0.123798 | 0.215808 | intron-variant | PLCG2 | GRCh38.p7 | 16:81892890 | TCTCACTCTGTTGCC[C/G]AGGCTGGAGTGCATT | 5336 |
| rs28530725 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | PLCG2 | GRCh38.p7 | 16:81920049 | AGAGAGGATAGCATG[C/T]GCAAAGGTCCTGAGG | 5336 |
| rs28531390 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PLCG2 | GRCh38.p7 | 16:81828490 | TGATCCACCCATCTC[A/G]GCCTCCCAAAGTGGT | 5336 |
| rs28531953 | snp | G/T | 0.5 | 0 | intron-variant | PLCG2 | GRCh38.p7 | 16:81866296 | GCTGGCCTCTCCCTT[G/T]CTCCCAGGATGAGCT | 5336 |
| rs28534531 | snp | A/G | 0.117886 | 0.21224 | intron-variant | PLCG2 | GRCh38.p7 | 16:81889410 | GACTGGTTAGCTGGG[A/G]TTGTTTCTTTTCTTT | 5336 |