Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17 4
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17 4
rs9261129
ZNRD1ASP
1.000 6 30011802 intron variant T/C snv 0.17 4
rs9261174
ZNRD1ASP
1.000 6 30029078 intron variant T/C snv 0.17 4
rs4313034
HLA-J ; ZNRD1ASP ; HLA-A
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 2
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23 2
rs3757333
ZNRD1 ; ZNRD1ASP
1.000 0.040 6 30060829 non coding transcript exon variant C/A snv 9.8E-02 1
rs4711207
ZNRD1ASP
1.000 0.120 6 30037977 intron variant C/A snv 0.23 1
rs166327
ZNRD1ASP
1.000 0.120 6 30035104 non coding transcript exon variant T/C snv 0.44 1
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 1
rs16896923
ZNRD1ASP ; ETF1P1
1.000 0.120 6 30032910 non coding transcript exon variant T/C snv 5.0E-02 1