Source: GWASDB ×
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 25
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs4820599
LRRC75B ; GGT1
0.925 0.160 22 24594246 intron variant A/G snv 0.43 3
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 2
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 2
rs12145922
PKN2-AS1
1 88680551 intron variant C/A snv 0.57 2
rs10908458 1 155154472 intergenic variant T/A;C snv 1
rs1497406 1 16178825 intergenic variant A/G snv 0.47 1
rs2739330 22 23953099 intron variant T/C snv 0.58 1
rs4503880 18 58416822 non coding transcript exon variant T/A;C snv 1
rs6888304 5 31020414 intergenic variant A/G snv 0.30 1
rs7786376 7 73628284 upstream gene variant A/G snv 0.28 1
rs12968116
ATP8B1 ; LOC100505549
18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 1
rs8038465
CD276
15 73685996 intron variant C/T snv 0.31 1