Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs10033366
ENPEP
4 110409934 intron variant T/C snv 0.92 1
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 2
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs148636776
ATXN2 ; SH2B3
0.790 0.280 12 111447491 missense variant G/A snv 1.5E-04 2.4E-04 1
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 3
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs2072134
OAS3
12 112971371 3 prime UTR variant G/A snv 3.7E-03 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs419598
IL1RN
0.742 0.280 2 113129630 synonymous variant T/C snv 0.26 0.21 1
rs180912 10 113982069 regulatory region variant T/G snv 0.56 1