List of variants in gene SPTBN2 reported as likely benign for Autosomal recessive spinocerebellar ataxia 14

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006946.4(SPTBN2):c.5950-8G>A	rs201759431	0.00277
NM_006946.4(SPTBN2):c.6896+11G>A	rs141969559	0.00203
NM_006946.4(SPTBN2):c.1807+13C>T	rs151122248	0.00132
NM_006946.4(SPTBN2):c.1351-7G>A	rs116078747

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