List of variants in gene combination ATXN1, LOC108663993 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001128164.2(ATXN1):c.624G>T (p.Gln208His)	rs28555263	0.00374
NM_001128164.2(ATXN1):c.621G>T (p.Gln207His)	rs201030692	0.00057
NM_001128164.2(ATXN1):c.630G>T (p.Gln210His)	rs368218879	0.00014
NM_001128164.2(ATXN1):c.636G>T (p.Gln212His)	rs376233432	0.00010
NM_001128164.2(ATXN1):c.588GCA[12] (p.Gln208del)	rs193922926
NM_001128164.2(ATXN1):c.633_635del (p.His211del)	rs759132871

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