List of variants in gene combination ATXN2, LOC130008791 reported as likely benign for dementia

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Gene type: Distinguish antisense genes from sense genes
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_001372574.1(ATXN2):c.57A>G (p.Gln19=)	rs76696028	0.13779
NM_001372574.1(ATXN2):c.59AGC[8] (p.Gln28del)	rs10560189

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