Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs7155454
FNTB ; MAX ; CHURC1-FNTB
14 65035521 intron variant G/A snv 0.61 4
rs4466998
MAX ; CHURC1-FNTB ; FNTB
14 65008822 intron variant C/A;G snv 2