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rs796052835

From SNPedia

ClinVar
Risk rs796052835(CT;CT)
Alt rs796052835(CT;CT)
Reference rs796052835(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661637_99661638dupAG
CLNSRC
CLNACC RCV000188396.1,