Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 5
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11