Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3088078
NFS1 ; ROMO1 ; RBM39
20 35700932 3 prime UTR variant C/T snv 6.0E-02 3.7E-02 2
rs17343651
RBM39
20 35708244 intron variant G/C snv 2.0E-02 2
rs6121037
RBM39
20 35742661 upstream gene variant G/C snv 0.11 2