Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 7
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 6
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 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
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 5