Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11051061
LOC645485 ; LINC00941
12 30761734 intron variant G/A snv 0.19 1
rs11055030
APOLD1 ; LOC107984129 ; LOC105369663
12 12725415 upstream gene variant G/C snv 0.23 1
rs11055034
APOLD1 ; LOC107984129
1.000 0.080 12 12737692 intron variant C/A;T snv 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs11085720
DNMT1
19 10207087 intron variant A/G snv 0.54 1
rs11096402
PLAC1
X 134693838 intron variant G/A snv 0.52 1
rs1112718 10 92719350 intergenic variant A/G snv 0.43 1
rs112139215
MLXIPL
7 73620229 intron variant C/A snv 4.1E-02 1
rs1129156
MAP3K10
19 40213169 synonymous variant T/C snv 0.73 0.75 1
rs113086489 17 7268037 upstream gene variant C/A;G;T snv 1
rs113510833 6 29703290 downstream gene variant C/T snv 6.7E-02 1
rs1151200
TENM4
11 79281641 intron variant T/C snv 0.50 1
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs116276359
THEM5 ; C2CD4D-AS1
1 151848954 intron variant C/A snv 1.5E-02 1
rs11630479
IGF1R
15 98697252 intron variant G/A snv 0.39 1
rs11641308 16 75278125 intergenic variant T/C snv 0.52 1
rs11646700
SMPD3
16 68387765 intron variant A/G snv 0.38 1
rs116807401
PABPC4L
4 134200566 missense variant T/C snv 8.8E-03 9.5E-03 1
rs11680809 2 112813232 downstream gene variant C/A snv 0.55 1
rs116964396
NKX6-3
8 41648330 intron variant C/A;T snv 1
rs11698914
COMMD7
20 32739337 intron variant C/A;G snv 1
rs11704481
FAM118A
22 45336447 intron variant G/A snv 0.49 0.42 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs11711420
LOC105374248
3 183631222 upstream gene variant T/A;G snv 1
rs11719201
ADCY5
3 123349897 intron variant C/T snv 0.20 1