Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2835931 | 1.000 | 0.120 | 21 | 37749345 | intron variant | C/A;T | snv | 4 | |||
rs477145 | 1.000 | 0.120 | 21 | 31390097 | intron variant | C/A;T | snv | 4 | |||
rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
rs1040411 | 1.000 | 0.120 | 6 | 106150148 | intron variant | G/A | snv | 0.47 | 3 | ||
rs1051660 | 1.000 | 0.080 | 8 | 53251002 | synonymous variant | C/A;T | snv | 0.11 | 3 | ||
rs1196644309 | 1.000 | 0.080 | 1 | 145995155 | missense variant | G/A | snv | 3 | |||
rs12881063 | 1.000 | 0.080 | 14 | 20788017 | downstream gene variant | G/C | snv | 7.4E-02 | 3 | ||
rs1340026226 | 1.000 | 0.080 | X | 67711662 | missense variant | G/A | snv | 9.5E-06 | 3 | ||
rs200081710 | 1.000 | 0.120 | 4 | 121154648 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
rs41281081 | 1.000 | 0.080 | 7 | 116796211 | 3 prime UTR variant | G/A | snv | 2.5E-03 | 3 | ||
rs4946728 | 1.000 | 0.120 | 6 | 106142488 | intron variant | A/C | snv | 0.72 | 3 | ||
rs754854286 | 1.000 | 0.120 | 10 | 31520432 | missense variant | G/C | snv | 3 | |||
rs76322625 | 1.000 | 0.080 | 7 | 116798111 | 3 prime UTR variant | C/A;T | snv | 3 | |||
rs10420252 | 1.000 | 0.080 | 19 | 35648270 | upstream gene variant | G/A | snv | 9.7E-02 | 2 | ||
rs11246050 | 1.000 | 0.080 | 11 | 284257 | synonymous variant | G/A;C | snv | 0.16; 4.0E-06 | 2 | ||
rs1131692237 | 1.000 | 0.040 | 17 | 39725161 | missense variant | T/G | snv | 2 | |||
rs1347591 | 1.000 | 0.080 | 16 | 56834788 | intron variant | A/G | snv | 0.47 | 0.47 | 2 | |
rs140451238 | 1.000 | 0.080 | 5 | 157208978 | synonymous variant | T/C | snv | 1.6E-04 | 7.8E-04 | 2 | |
rs1410727652 | 1.000 | 0.080 | 6 | 160348669 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs2118593 | 1.000 | 0.080 | 3 | 72447740 | upstream gene variant | G/A;C;T | snv | 2 | |||
rs2286742 | 1.000 | 0.080 | 10 | 113580733 | intron variant | G/A;C | snv | 0.57; 8.2E-06 | 2 | ||
rs2336219 | 1.000 | 0.080 | 19 | 45409148 | missense variant | G/A | snv | 0.21 | 0.19 | 2 | |
rs33954691 | 1.000 | 0.080 | 5 | 1255405 | synonymous variant | G/A | snv | 0.13 | 9.0E-02 | 2 | |
rs353630 | 1.000 | 0.080 | 11 | 35166644 | intron variant | G/A | snv | 0.33 | 2 | ||
rs367722824 | 1.000 | 0.120 | 4 | 54278512 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 2 |