Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758946412
rs758946412
Entrez Id: 57526
Gene Symbol: PCDH19
PCDH19
CUI: C4024965
Disease:
Frontal cortical atrophy
CG 0.700 CausalMutation CLINVAR