rs80338941, GJB2

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.
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 1.000 0.120 13 20189526 missense variant C/A;G snv 2.8E-05; 1.2E-05 0.710 1.000 1 2005 2005
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
98 1.000 0.120 13 20189526 missense variant C/A;G snv 2.8E-05; 1.2E-05 0.700 0