Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894408
rs104894408
GJB2
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		G 0.850 CausalMutation CLINVAR

dbSNP: rs104894408
rs104894408
GJB2
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		A 0.850 GeneticVariation CLINVAR