Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-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
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
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
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs7085433
TIMM23
1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 4
rs73728279
PRKAG2
1.000 0.080 7 151714408 intron variant G/A;T snv 4