Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs281875330
rs281875330
ACTG1 ; FSCN2
1.000 0.120 17 81511626 missense variant T/C snv
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.010 1.000 1 2008 2008