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rs387906942

From SNPedia

ClinVar
Risk rs387906942(G;G)
Alt rs387906942(G;G)
Reference rs387906942(C;C)
Significance Other
Disease Parkinson disease 13
Variation info
Gene HTRA2 AUP1
CLNDBN Parkinson disease 13
Reversed 0
HGVS NC_000002.11:g.74757560C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023546.3,