Source: CLINVAR

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: rs879253799
rs879253799
DCAF17
0.882 0.320 2 171443559 frameshift variant A/- delins
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.700 1.000 1 2016 2016