Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62 4
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 4
rs9399136
HBS1L
6 135081201 intron variant T/C snv 0.18 4
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 4
rs4791641
PFAS
17 8257831 missense variant C/T snv 0.43 0.41 4
rs73728279
PRKAG2
1.000 0.080 7 151714408 intron variant G/A;T snv 4