SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs742210 | snp | A/G | 0.225005 | 0.248747 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41139104 | CCTTCCTTCCTCCCA[A/G]TCTCCTCAACTATCT | 5335 |
rs753381 | snp | A/G | 0.473313 | 0.112389 | missense, upstream-variant-2KB, nc-transcript-variant | PLCG1, MIR6871 | GRCh38.p7 | 20:41168825 | ATGATGGCGCTCTTG[A/G]TGAAGGTCAGCTCGT | 5335 |
rs760762 | snp | C/T | 0.456095 | 0.141508 | intron-variant | PLCG1 | GRCh38.p7 | 20:41147406 | AGAACTGGTCTACAC[C/T]GGAAGCATGAAGCTC | 5335 |
rs760763 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PLCG1 | GRCh38.p7 | 20:41164548 | TTGTCTCTGTTCCCT[A/G]TGTCCCATTCCTTCA | 5335 |
rs760764 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PLCG1 | GRCh38.p7 | 20:41171166 | TTGGAGAGGGCACCC[A/G]CAAGCCAAATAGAGA | 5335 |
rs909708 | snp | C/T | 0.145789 | 0.227245 | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41169006 | CTTAGGCATGGGAAC[C/T]CCTACCAAAGGATAC | 5335 |
rs926345 | snp | C/T | 0.461148 | 0.133852 | intron-variant | PLCG1 | GRCh38.p7 | 20:41143307 | CCTTTTCCTGTGGGA[C/T]GTGGCTTCAAGGAGA | 5335 |
rs2072880 | snp | A/T | 0.104539 | 0.203325 | intron-variant | PLCG1 | GRCh38.p7 | 20:41170433 | TGAGAAGAAACAGAC[A/T]CATAAGATGCAATGT | 5335 |
rs2072881 | snp | C/T | 0.493969 | 0.05458 | intron-variant | PLCG1 | GRCh38.p7 | 20:41159297 | TGGGTCCCTATTTCT[C/T]CTTCTGGAGTCTAGC | 5335 |
rs2072882 | snp | A/T | 0.227959 | 0.249026 | intron-variant | PLCG1 | GRCh38.p7 | 20:41159371 | GAAGGGACACCCCAC[A/T]GAACCACCTTTCCCC | 5335 |
rs2076145 | snp | C/T | 0.134968 | 0.221963 | intron-variant | PLCG1 | GRCh38.p7 | 20:41163898 | ATCTGACCATACCTA[C/T]CTGCCTCTCCTTGCC | 5335 |
rs2076146 | snp | C/G | 0.45574 | 0.142025 | intron-variant | PLCG1 | GRCh38.p7 | 20:41169778 | AACAAAGTTGATGCT[C/G]CTGGTTGGCTGACAT | 5335 |
rs2076148 | snp | A/G | 0.463126 | 0.13068 | intron-variant | PLCG1 | GRCh38.p7 | 20:41160215 | TCCAGAACCTTAGCC[A/G]GGCCTCTAAGTAGCT | 5335 |
rs2228246 | snp | A/G | 0.23547 | 0.249577 | missense, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41163423 | CAGGAGTTCATGCTC[A/G]GCTTCCTCCGAGACC | 5335 |
rs2229348 | snp | A/C | 0.000418113 | 0.0144527 | missense, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41162670 | GCAGCGGGGACATCA[A/C]CTACGGGCAGTTTGC | 5335 |
rs2235360 | snp | C/T | 0.234982 | 0.249549 | intron-variant | PLCG1 | GRCh38.p7 | 20:41172070 | GGTGTCTGGAAGGTA[C/T]AGGGGAAGGTGGGAG | 5335 |
rs2235361 | snp | C/T | 0.465374 | 0.126941 | missense, intron-variant, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41172230 | AACGGAGGAAGAAGA[C/T]TGCCCTGGAGCTCTC | 5335 |
rs2866370 | snp | A/G | 0.109814 | 0.206997 | intron-variant | PLCG1 | GRCh38.p7 | 20:41146854 | TGACTTCAGCCTAAG[A/G]CCCAGAGAGTGTGGG | 5335 |
rs2866371 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PLCG1 | GRCh38.p7 | 20:41157134 | GCTTACCTGGTTCCT[A/G]TCTCAGGCACCTGTT | 5335 |
rs3082120 | snp | C/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41157241 | gtgtgtgtgtgtgtg[C/T]ACAGTCACACTCACC | 5335 |
rs3795128 | snp | A/G | 0.460702 | 0.134554 | intron-variant | PLCG1 | GRCh38.p7 | 20:41145523 | CAGAGTAGGCTCAGC[A/G]GGCAGCTCAAGTAGG | 5335 |
rs3795130 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | PLCG1 | GRCh38.p7 | 20:41141396 | GCAGTTAGCTGTTTT[A/C]TTCCGCCACCCTCAC | 5335 |
rs3795131 | snp | A/G | 0.496382 | 0.0423778 | intron-variant | PLCG1 | GRCh38.p7 | 20:41141335 | TCATTGCCTGTTTTC[A/G]TTTCCCTAAAAGCAA | 5335 |
rs6016518 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | PLCG1 | GRCh38.p7 | 20:41142803 | tgtataaagtgctta[A/G]cacctgtataaagtg | 5335 |
rs6016519 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | PLCG1 | GRCh38.p7 | 20:41151715 | ACAGGCTTTGGGCAT[A/T]TGCAGCCAGCTTGGA | 5335 |
rs6016520 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | PLCG1 | GRCh38.p7 | 20:41161260 | GTGGTGAAATCTGAC[C/G]GTTGACCCTTGGATT | 5335 |
rs6016521 | snp | C/G | 0.0052846 | 0.0511309 | intron-variant | PLCG1 | GRCh38.p7 | 20:41165107 | CCTCATCAAGGTGGG[C/G]TGGCGGGCTTATTGC | 5335 |
rs6016522 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41167521 | CAGCAGTGAACCAAC[A/G]AGCCACTGAACTAAA | 5335 |
rs6029554 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PLCG1 | GRCh38.p7 | 20:41143832 | TAAGGGAGATTATAT[A/G]TAAGAGTAAGAGATT | 5335 |
rs6029556 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PLCG1 | GRCh38.p7 | 20:41169643 | AAGTCTGCCCTCACT[C/T]CAAGCTCTCCCCATG | 5335 |
rs6029557 | snp | C/T | 0.0052282 | 0.0508603 | intron-variant | PLCG1 | GRCh38.p7 | 20:41172372 | TAGGTATCCCCCCAA[C/T]ACTTCCTGGGTGGGC | 5335 |
rs6029559 | snp | C/T | 0 | 0 | downstream-variant-500B | PLCG1 | GRCh38.p7 | 20:41176150 | AAGGCCCTTCTCTTC[C/T]TGAAGCTCTGTTTCC | 5335 |
rs6065315 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41139563 | ttaccttctctgagc[C/T]ttgatttcctcatgt | 5335 |
rs6065316 | snp | C/T | | | missense, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41165078 | CCCTCACCCAACCAG[C/T]TTAAGAGGAAGATCC | 5335 |
rs6065317 | snp | A/C/G | 4.94485e-05 | 0.00497214 | intron-variant | PLCG1 | GRCh38.p7 | 20:41166662 | TGACCCTGTGTGACT[A/C/G]TTTTGTCCTTGTGAA | 5335 |
rs6072282 | snp | A/C | 0 | 0 | intron-variant | PLCG1 | GRCh38.p7 | 20:41141825 | AGATAACTGGAGGAG[A/C]TGAGCACACCCAGTC | 5335 |
rs6072285 | snp | A/G | 0.144632 | 0.226711 | intron-variant | PLCG1 | GRCh38.p7 | 20:41147805 | GTGAGCCAAGATCGC[A/G]CCATTGCACTCCAGC | 5335 |
rs6072286 | snp | A/G | 0.163564 | 0.234582 | intron-variant | PLCG1 | GRCh38.p7 | 20:41156589 | AGTGACGGCCTCTTC[A/G]TACCCCTGGCTTTTC | 5335 |
rs6072289 | snp | A/T | 0.0912534 | 0.193131 | intron-variant | PLCG1 | GRCh38.p7 | 20:41161995 | GACCAAACTCCCAGC[A/T]TCCCAGTGGGCAGCA | 5335 |
rs6072292 | snp | A/G | | | splice-acceptor-variant | PLCG1 | GRCh38.p7 | 20:41166475 | CTCTGCCTGTTCTCA[A/G]GTGGTACCACGCGAG | 5335 |
rs6093444 | snp | C/T | 0.108048 | 0.20579 | intron-variant | PLCG1 | GRCh38.p7 | 20:41149968 | ggaggccaagactgg[C/T]gagtcatttgagccc | 5335 |
rs6093446 | snp | A/G | 0.473359 | 0.112298 | intron-variant | PLCG1 | GRCh38.p7 | 20:41152292 | AGGGCGTGGGTGCTC[A/G]GCATCCTGCTGCTTT | 5335 |
rs6102290 | snp | A/G | 0 | 0 | intron-variant | PLCG1 | GRCh38.p7 | 20:41140877 | ATCGTTTGTGCCCAA[A/G]GTGTTGTGTCAGTGT | 5335 |
rs6102291 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PLCG1 | GRCh38.p7 | 20:41153463 | gtctagctaagtttt[C/T]ttaatttttattttt | 5335 |
rs6102292 | snp | G/T | 0.097727 | 0.198275 | intron-variant | PLCG1 | GRCh38.p7 | 20:41156994 | TGGCTTTCAAGAACC[G/T]AGTAGAGCATCTCAC | 5335 |
rs6102294 | snp | C/T | 0.0444908 | 0.142359 | intron-variant, utr-variant-5-prime | PLCG1 | GRCh38.p7 | 20:41162387 | agccCCAGGTGGGCT[C/T]GACCCACAGGTCAGA | 5335 |
rs6102295 | snp | A/G | 0.0883596 | 0.190715 | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41167032 | AGGGTGTCTGCAGGA[A/G]GGGACATCTGAGCAG | 5335 |
rs6124323 | snp | A/G | 0.495811 | 0.045573 | intron-variant | PLCG1 | GRCh38.p7 | 20:41165849 | TTCCCATGCAGATGC[A/G]TATGTTCAGTCAGCG | 5335 |
rs7265284 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PLCG1 | GRCh38.p7 | 20:41158316 | CACTGCATCTGGCTC[C/T]GAAGTTACCAGGCCA | 5335 |
rs7266677 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41164186 | CCATCAAGGAGCATG[C/T]CTTTGTGGCCTCAGA | 5335 |
rs7273590 | snp | C/G | 0 | 0 | intron-variant | PLCG1 | GRCh38.p7 | 20:41155025 | AGTAACTGCTGGTCT[C/G]TAATCTCTGTGGTCT | 5335 |
rs7274650 | snp | A/C | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41151560 | CACCCCTCCACTTTG[A/C]CCTTCCTTTGGTGGC | 5335 |
rs7360710 | snp | C/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41165147 | ACACTTCTCAGTGCC[C/T]TGCCCAGGCCATGGC | 5335 |
rs7361272 | snp | G/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41158452 | TAAATCGGTGATTTC[G/T]GGGCTGGAATGTCTG | 5335 |
rs7363553 | snp | A/C | | | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41168651 | GCAGTGTCATCTCCC[A/C]CTGGCCTGACCCCAG | 5335 |
rs8122204 | snp | A/G | 0.0290588 | 0.116983 | intron-variant | PLCG1 | GRCh38.p7 | 20:41165864 | ATATGTTCAGTCAGC[A/G]TGTGTACACAGACAT | 5335 |
rs8183460 | snp | C/G | | | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41169007 | TTAGGCATGGGAACC[C/G]CTACCAAAGGATACC | 5335 |
rs8183966 | snp | C/T | | | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41138045 | GGGGCATCCGGGTCC[C/T]CGGTCACCTGACAGG | 5335 |
rs11426520 | in-del | -/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41162236 | TTGTTTTGTTTTTGT[-/T]TTTTTTTTTTTTTTT | 5335 |
rs11473325 | in-del | -/TGTA | 0.125742 | 0.216933 | intron-variant | PLCG1 | GRCh38.p7 | 20:41169814 | GCCTAATGGGTTGTA[-/TGTA]CCACAGGGATGTGAC | 5335 |
rs11547263 | snp | A/C/T | 6.5919e-05 | 0.00574073 | synonymous-codon, stop-gained, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41162522 | AACATGCGCTTCCTC[A/C/T]GAGAGCGGCTGACGG | 5335 |
rs11696662 | snp | C/T | 0.079617 | 0.182947 | intron-variant | PLCG1 | GRCh38.p7 | 20:41161795 | TCCTGTTGCCAGGTC[C/T]AGCAGTGTCCCCAGC | 5335 |
rs12106101 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | PLCG1 | GRCh38.p7 | 20:41146297 | GAAAACCGCTAATGC[C/G]CAGGGCTGGCAGGAG | 5335 |
rs12480560 | snp | C/T | 0.225597 | 0.248806 | intron-variant | PLCG1 | GRCh38.p7 | 20:41152242 | CCTGGGACCACTCTC[C/T]TGAATCTCCTCATGG | 5335 |
rs12480979 | snp | C/T | 0 | 0 | intron-variant | PLCG1 | GRCh38.p7 | 20:41141281 | TCACTAGATACTTTT[C/T]TAGATGCCAGGCCCT | 5335 |
rs12624863 | snp | A/G | 0.357024 | 0.225933 | intron-variant | PLCG1 | GRCh38.p7 | 20:41154259 | TCTGTCTGTTGGGCT[A/G]TTTGGAAGTGGCTTT | 5335 |
rs12625708 | snp | A/C | 0.356383 | 0.226236 | intron-variant | PLCG1 | GRCh38.p7 | 20:41154394 | GCCATGTGTCTGCCC[A/C]CTAGGGCAGGATTGG | 5335 |
rs13037246 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41139852 | AGATTGCTACTCAGA[A/G]AAAGGCAGGAAACAG | 5335 |
rs13433162 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | PLCG1 | GRCh38.p7 | 20:41157814 | AGAGGGCAAAAGCTG[A/G]GGAGGTAAATTCCTG | 5335 |
rs16989589 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PLCG1 | GRCh38.p7 | 20:41169941 | GACTTGTTTGAGTTG[C/T]AGCGTCGTCATCTGT | 5335 |
rs28362587 | snp | G/T | 0.220544 | 0.248259 | upstream-variant-2KB, intron-variant | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41137160 | CGCGGGGTAGCGGCC[G/T]CCCGTGCGAGTACGC | 5335 |
rs28479848 | snp | C/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41144208 | GGAGAAAACCAAGCC[C/T]TAAGGGTAAGGTCAC | 5335 |
rs33917926 | snp | A/C | 0.0365129 | 0.130089 | synonymous-codon, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41174174 | TGAGGCATCTGAGCC[A/C]CGCTCCCGCAGGGAC | 5335 |
rs33928471 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | PLCG1, MIR6871 | GRCh38.p7 | 20:41169392 | TTTGTCCCATGCACA[C/T]GGATATCCCCTCACA | 5335 |
rs33943601 | snp | A/G | 0.0247852 | 0.108528 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41172488 | TTTGGCCTTGTTCAC[A/G]TATTTCTCAGCCTTG | 5335 |
rs33947984 | snp | G/T | 0.079617 | 0.182947 | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41167427 | AGGCCTGTTGTCCAC[G/T]GGCACCTGGGACTCA | 5335 |
rs34012203 | snp | C/T | 0.00803863 | 0.0628864 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PLCG1, MIR6871 | GRCh38.p7 | 20:41169148 | GGAAGAGATGGTCAA[C/T]CCCGTGGCCCTGGAG | 5335 |
rs34064713 | snp | A/G | 0.00171464 | 0.0292298 | intron-variant | PLCG1 | GRCh38.p7 | 20:41164218 | TGAGTCGGAGGCTGG[A/G]TGACCCAGGGGTTAA | 5335 |
rs34065911 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | PLCG1 | GRCh38.p7 | 20:41144154 | ACAGCAGCTCCATGA[A/G]TCCATGGAGGGCAGG | 5335 |
rs34068306 | snp | C/T | 0.0105817 | 0.0719645 | intron-variant | PLCG1 | GRCh38.p7 | 20:41170451 | TAAGATGCAATGTGG[C/T]GTGTTTAGGTTGTGT | 5335 |
rs34081340 | snp | C/G | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41136993 | CGCCGCCGCCGGTGT[C/G]AGGCGGCCCGTCCTG | 5335 |
rs34115001 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PLCG1 | GRCh38.p7 | 20:41150681 | CCTCCCTTCTCATCC[A/G]TGATACTCTGAATGC | 5335 |
rs34121619 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PLCG1 | GRCh38.p7 | 20:41148685 | CAAGGAGTTTACGCT[C/G]TAGTGGAGAAAACAA | 5335 |
rs34130768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PLCG1, MIR6871 | GRCh38.p7 | 20:41167085 | CACATAAGCAGAGGG[C/T]TCCTCATGAGTCAAG | 5335 |
rs34150127 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | PLCG1 | GRCh38.p7 | 20:41144301 | CCATTCTGGGGAAAA[A/T]GATAATAGGATGGAC | 5335 |
rs34162104 | in-del | -/G | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41151917 | CTGCCTGTGAAGGGG[-/G]ATCTGCAGTGCAGTG | 5335 |
rs34183705 | snp | C/T | 0.00117448 | 0.0242045 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41170263 | GGCCCAGACAGCAGA[C/T]GCCAGGGTGAGATTC | 5335 |
rs34186698 | snp | C/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41138780 | GGCTGCTTTTGCGCT[C/G]GTCTCTAGTGGGAGG | 5335 |
rs34203315 | snp | C/G | 0.000461194 | 0.0151784 | missense, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41166774 | TTGTTGACCTCATCA[C/G]CTACTATGAGAAACA | 5335 |
rs34206101 | snp | G/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41138957 | ACTGGGTTGCTTCTT[G/T]CAGGGACCCCCGGAG | 5335 |
rs34222470 | snp | C/T | 0.00344727 | 0.0413733 | intron-variant | PLCG1 | GRCh38.p7 | 20:41163362 | CTCTCATCCCCTGCC[C/T]TCCCTACCCCATCAG | 5335 |
rs34234873 | in-del | -/G | 0.0215028 | 0.101435 | intron-variant, upstream-variant-2KB | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41139764 | GGAATGGTGAGGGGG[-/G]TGAGGTGTGGCTATA | 5335 |
rs34255699 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PLCG1, PLCG1-AS1 | GRCh38.p7 | 20:41135955 | TGAGAGATGAAACTG[A/G]TGAGATGGGCAGGTC | 5335 |
rs34270358 | snp | G/T | 0.0105817 | 0.0719645 | intron-variant | PLCG1 | GRCh38.p7 | 20:41154875 | GTATAGCTTCACAGC[G/T]CCCAGAGTGCTTGGG | 5335 |
rs34273582 | snp | A/T | 0.144969 | 0.226867 | intron-variant | PLCG1 | GRCh38.p7 | 20:41150909 | TCTGTTTCCTCCATC[A/T]GGCAGGGGTTTTCTC | 5335 |
rs34278197 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PLCG1 | GRCh38.p7 | 20:41161877 | GTTTCTTTCCTGGAG[C/T]CAGGCCCTGTCTAGC | 5335 |
rs34283671 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PLCG1 | GRCh38.p7 | 20:41159691 | CCCAGCTTTCCGGCC[A/G]GACCAGTCACATTGC | 5335 |
rs34325936 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PLCG1 | GRCh38.p7 | 20:41176054 | AAATGTTGCATTCAG[C/T]TCGTTAACACTGCCA | 5335 |
rs34334432 | in-del | -/T | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41157870 | GCCATAGAAGGTGTT[-/T]GTTGTTTGTTCTCCT | 5335 |
rs34363000 | in-del | -/C | | | intron-variant | PLCG1 | GRCh38.p7 | 20:41146988 | AAGGAATACAACTCC[-/C]ATTCCCTCAGTTGGG | 5335 |