rs1565402473, MYO7A

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
DEAFNESS, AUTOSOMAL RECESSIVE 2
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
135 1.000 0.120 11 77179098 frameshift variant G/- delins 0.700 0
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 1.000 0.120 11 77179098 frameshift variant G/- delins 0.700 0