Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753381
PLCG1 ; MIR6871
20 41168825 missense variant T/C snv 0.61 0.67 1
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs12461110
NLRP11
19 55809297 missense variant G/A snv 0.32 0.26 1
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs2960051 18 30276169 intergenic variant C/T snv 0.84 1
rs3107997
LOC105372047 ; LOC105372046
18 30340278 intron variant C/T snv 0.21 1
rs4564656 18 30301067 intron variant G/A snv 0.76 1
rs6508654 18 30302598 intron variant T/C snv 0.81 1
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 1
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 1
rs339969
RORA ; RORA-AS1
15 60591082 intron variant C/A snv 0.68 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs7968682 12 65978100 intergenic variant G/T snv 0.56 1
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs1151200
TENM4
11 79281641 intron variant T/C snv 0.50 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs10788038 10 120117008 intergenic variant T/C snv 0.61 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1