Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356460
rs80356460
Entrez Id: 6495;113218481
Gene Symbol: SIX1;MIR9718
SIX1;MIR9718
CUI: C1854594
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 23
T 0.700 CausalMutation CLINVAR