Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1709832
KCNJ6
1.000 0.080 21 37665865 intron variant T/G snv 0.57 3
rs1787331
KCNJ6
1.000 0.080 21 37631223 intron variant T/G snv 0.68 3
rs4452239
KCNJ6
1.000 0.080 21 37680353 intron variant T/G snv 0.50 3
rs73220491
KCNJ6
1.000 0.080 21 37616021 3 prime UTR variant T/G snv 0.31 3
rs857975
KCNJ6
1.000 0.080 21 37629311 intron variant T/G snv 0.71 3
rs1800759
LOC100507053 ; ADH4
0.925 0.120 4 99144358 intron variant T/G snv 0.49 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs8040009
C15orf32
1.000 0.080 15 92501109 non coding transcript exon variant T/C;G snv 3
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 11
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs10483038
KCNJ6
1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs11075992
FTO
1.000 0.080 16 53786154 intron variant T/C snv 0.41 3
rs1515050
KCNJ6
1.000 0.080 21 37630840 intron variant T/C snv 0.75 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1709818
KCNJ6
1.000 0.080 21 37663909 intron variant T/C snv 0.57 3
rs17125651 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 3
rs1867877
LOC105376579 ; IGSF22
1.000 0.080 11 18705901 missense variant T/C snv 3.5E-02 4.2E-02 3
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24 3
rs2835831
KCNJ6
1.000 0.080 21 37614931 3 prime UTR variant T/C snv 0.29 3
rs2835839
KCNJ6
1.000 0.080 21 37618732 3 prime UTR variant T/C snv 0.25 3
rs2835849
KCNJ6
1.000 0.080 21 37639222 intron variant T/C snv 0.27 3