Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11945758 1.000 0.040 4 117746079 intergenic variant G/A;T snv 1
rs11952719 1.000 0.040 5 106755127 regulatory region variant C/T snv 0.45 1
rs1198588 1.000 0.040 1 98087276 intergenic variant A/T snv 0.78 1
rs1198589 1.000 0.040 1 98084855 intergenic variant T/C snv 0.85 1
rs12001041 1.000 0.040 9 135600269 upstream gene variant A/G snv 0.20 1
rs12071951 1.000 0.040 1 96648359 intergenic variant T/G snv 0.27 1
rs12129037 1.000 0.040 1 150519638 downstream gene variant T/C;G snv 1
rs12139672 1.000 0.040 1 190971497 intron variant A/G snv 0.19 1
rs12140439 1.000 0.040 1 177753772 intron variant C/A snv 0.24 1
rs12190758 1.000 0.040 6 92438623 intergenic variant A/G snv 0.21 1
rs12325245 1.000 0.040 16 58647489 intergenic variant A/T snv 0.15 1
rs12360997 1.000 0.040 11 24364023 intergenic variant A/G snv 0.41 1
rs12363019 1.000 0.040 11 24352999 intergenic variant T/A snv 0.37 1
rs12374311 1.000 0.040 4 160303402 intergenic variant A/G;T snv 1
rs12434701 1.000 0.040 14 77643001 intergenic variant C/G;T snv 1
rs12446487 1.000 0.040 16 58637911 regulatory region variant A/C;T snv 1
rs12526618 1.000 0.040 6 145001120 intergenic variant A/T snv 0.26 1
rs12567918 1.000 0.040 1 204057325 regulatory region variant T/C snv 0.49 1
rs12625774 1.000 0.040 20 57412108 downstream gene variant C/A;T snv 1
rs12732868 1.000 0.040 1 5274577 regulatory region variant T/G snv 6.0E-02 1
rs12908161 1.000 0.040 15 84664594 downstream gene variant A/G snv 0.20 1
rs12915820 1.000 0.040 15 81716770 intron variant T/G snv 0.31 1
rs12965304 1.000 0.040 18 59420831 intergenic variant C/T snv 0.14 1
rs13008971 1.000 0.040 2 8840342 upstream gene variant A/C snv 0.58 1
rs13027106 1.000 0.040 2 76228042 intron variant T/C snv 0.18 1