Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7148590
CHURC1-FNTB ; FNTB ; MAX
14 65006478 intron variant G/A snv 0.57 3
rs2120019
PPCDC
15 75041843 intron variant T/C snv 0.31 2
rs11232535 11 81217766 intron variant T/C snv 0.15 1
rs11763353 7 15591246 intergenic variant A/G snv 0.21 1
rs1532423
CA1
8 85356084 intron variant A/G;T snv 1
rs4826508
NBDY
X 56785262 intron variant C/T snv 1