List of variants in gene ATXN2 reported as likely benign for Huntington disease and related disorders

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001372574.1(ATXN2):c.42G>A (p.Gln14=)	rs4098854	0.75596
NM_001372574.1(ATXN2):c.3043-12G>A	rs2073950	0.19844
NM_001372574.1(ATXN2):c.289-11del	rs144235483

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