STRC, stereocilin, 161497

N. diseases: 25; N. variants: 12
Disease: Deafness, Autosomal Recessive 16 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727503443
rs727503443
Entrez Id: 1159;161497
Gene Symbol: CKMT1B;STRC
CKMT1B;STRC
CUI: C1863561
Disease:
Deafness, Autosomal Recessive 16 		G 0.700 GeneticVariation CLINVAR