Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs962554
ADGRG6
6 142413067 intron variant T/C snv 0.40 2
rs10788038 10 120117008 intergenic variant T/C snv 0.61 1
rs1151200
TENM4
11 79281641 intron variant T/C snv 0.50 1
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs12461110
NLRP11
19 55809297 missense variant G/A snv 0.32 0.26 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 1
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 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
rs339969
RORA ; RORA-AS1
15 60591082 intron variant C/A snv 0.68 1
rs4564656 18 30301067 intron variant G/A snv 0.76 1
rs6508654 18 30302598 intron variant T/C snv 0.81 1
rs753381
PLCG1 ; MIR6871
20 41168825 missense variant T/C snv 0.61 0.67 1
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs7849941
LOC107987088
9 85130318 intergenic variant A/T snv 0.27 1
rs7968682 12 65978100 intergenic variant G/T snv 0.56 1