Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 1
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv 1
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70 1
rs4432842 1.000 0.080 5 57876251 intergenic variant T/C snv 0.45 1
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs962554
ADGRG6
6 142413067 intron variant T/C snv 0.40 2
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1
rs809871
LOC105374986
6 26256298 downstream gene variant C/G;T snv 1
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 1
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs7849941
LOC107987088
9 85130318 intergenic variant A/T snv 0.27 1
rs930811 9 2696555 intergenic variant G/A snv 0.47 1