ClinVar Miner

List of variants in gene HTRA2, LOC129934140 studied for Parkinson disease 13, autosomal dominant, susceptibility to

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_013247.5(HTRA2):c.507-10T>A rs747756166
NM_013247.5(HTRA2):c.507-9C>A rs151291127

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