Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115460205
FSTL5
1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs12482570
LOC107985507 ; KCNJ6
1.000 0.080 21 37705475 intron variant A/G snv 0.30 3
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs1316543
GRK5
1.000 0.080 10 119445148 intron variant G/A snv 0.15 3
rs1399590
KCNJ6
1.000 0.080 21 37681768 intron variant G/A snv 0.56 3
rs1399591
KCNJ6
1.000 0.080 21 37681654 intron variant C/T snv 0.50 3
rs1399592
KCNJ6
1.000 0.080 21 37681559 intron variant T/A;G snv 0.52 3
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1475839
KCNJ6
1.000 0.080 21 37649639 intron variant C/T snv 0.31 3
rs1515050
KCNJ6
1.000 0.080 21 37630840 intron variant T/C snv 0.75 3
rs1515056
LOC107985507 ; KCNJ6
1.000 0.080 21 37710283 intron variant C/G;T snv 0.28 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81 3
rs1709817
KCNJ6
1.000 0.080 21 37664047 intron variant T/A;C snv 3
rs1709818
KCNJ6
1.000 0.080 21 37663909 intron variant T/C snv 0.57 3
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3
rs1709820
KCNJ6
1.000 0.080 21 37663669 intron variant A/C snv 0.57 3
rs1709826
KCNJ6
1.000 0.080 21 37677171 intron variant G/A;C snv 3
rs1709832
KCNJ6
1.000 0.080 21 37665865 intron variant T/G snv 0.57 3
rs1709833
KCNJ6
1.000 0.080 21 37665503 intron variant A/G snv 0.57 3