Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs540606 1.000 0.080 2 44911368 intergenic variant A/G snv 0.66 3
rs1995364 1.000 0.080 5 10903669 intergenic variant A/G snv 0.62 1
rs7777391 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 1
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 3
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs1787394
KCNJ6
1.000 0.080 21 37663874 intron variant C/A snv 0.58 3
rs1709818
KCNJ6
1.000 0.080 21 37663909 intron variant T/C snv 0.57 3
rs1709820
KCNJ6
1.000 0.080 21 37663669 intron variant A/C snv 0.57 3
rs1787397
KCNJ6
1.000 0.080 21 37665076 intron variant A/G snv 0.57 3
rs8134288
KCNJ6
1.000 0.080 21 37664687 intron variant T/C snv 0.57 3
rs1787399
KCNJ6
1.000 0.080 21 37665581 intron variant A/G snv 0.57 3
rs1709832
KCNJ6
1.000 0.080 21 37665865 intron variant T/G snv 0.57 3
rs1787400
KCNJ6
1.000 0.080 21 37665915 intron variant G/C snv 0.57 3
rs1709833
KCNJ6
1.000 0.080 21 37665503 intron variant A/G snv 0.57 3
rs1787398
KCNJ6
1.000 0.080 21 37665202 intron variant A/C snv 0.57 3
rs1709835
KCNJ6
1.000 0.080 21 37665334 intron variant A/C;G snv 0.57 3
rs1787396
KCNJ6
1.000 0.080 21 37664185 intron variant A/C snv 0.57 3
rs1399590
KCNJ6
1.000 0.080 21 37681768 intron variant G/A snv 0.56 3
rs9512637 1.000 0.080 13 27346474 upstream gene variant T/C snv 0.55 3
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs3736802
TRPC4AP
1.000 0.080 20 35016239 intron variant T/C snv 0.53 3
rs4817881
KCNJ6
1.000 0.080 21 37659600 non coding transcript exon variant C/T snv 0.53 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3