Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 13 | ||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 6 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 6 | |
rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 6 | ||
rs34712979 | 1.000 | 0.040 | 4 | 105897896 | splice region variant | G/A;T | snv | 0.17 | 5 | ||
rs755249 | 1 | 39529402 | 3 prime UTR variant | C/A;T | snv | 5 | |||||
rs13116999 | 4 | 144521212 | intron variant | G/A | snv | 0.65 | 4 | ||||
rs1513272 | 7 | 28160478 | intron variant | C/T | snv | 0.40 | 4 | ||||
rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 4 | |||
rs6780171 | 3 | 185785668 | intron variant | T/A | snv | 0.39 | 4 | ||||
rs7424771 | 2 | 160419867 | intron variant | G/A | snv | 0.44 | 4 | ||||
rs7752448 | 6 | 28333322 | intron variant | A/G | snv | 0.15 | 4 | ||||
rs1008833 | 1 | 204457167 | intron variant | A/G | snv | 0.12 | 3 | ||||
rs10998018 | 10 | 68203197 | intron variant | G/A | snv | 0.41 | 3 | ||||
rs1102077 | 6 | 139950220 | intron variant | A/C | snv | 0.21 | 3 | ||||
rs11176001 | 12 | 66015587 | regulatory region variant | C/A | snv | 9.6E-02 | 3 | ||||
rs11191841 | 10 | 103879853 | 3 prime UTR variant | T/C | snv | 0.47 | 3 | ||||
rs11722225 | 4 | 105845273 | intron variant | T/C | snv | 5.5E-02 | 3 | ||||
rs12096239 | 1 | 26470431 | 3 prime UTR variant | G/C | snv | 0.23 | 3 | ||||
rs12331869 | 4 | 55145982 | intergenic variant | A/G | snv | 0.76 | 3 | ||||
rs12481092 | 20 | 46858178 | upstream gene variant | C/T | snv | 0.21 | 3 | ||||
rs12698403 | 7 | 156334552 | intergenic variant | G/A | snv | 0.40 | 3 | ||||
rs12707691 | 7 | 84940194 | non coding transcript exon variant | C/G | snv | 0.24 | 3 |