Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs11021221 11 95575690 intron variant T/A;G snv 4
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs778387 1 56158423 intron variant C/A;G;T snv 4
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs1694068
ARL15
5 53987800 intron variant T/A snv 0.62 4
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 4
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4