Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 1
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1
rs7849941
LOC107987088
9 85130318 intergenic variant A/T snv 0.27 1
rs339969
RORA ; RORA-AS1
15 60591082 intron variant C/A snv 0.68 1
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs809871
LOC105374986
6 26256298 downstream gene variant C/G;T snv 1
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 1
rs2960051 18 30276169 intergenic variant C/T snv 0.84 1
rs3107997
LOC105372047 ; LOC105372046
18 30340278 intron variant C/T snv 0.21 1