ClinVar Miner

List of variants reported as benign for Huntington disease and related disorders by Mendelics

Included ClinVar conditions (18):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001386393.1(PANK2):c.2T>A	rs71647828	0.06976
NM_001128164.2(ATXN1):c.772G>T (p.Gly258Cys)	rs144962740

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