List of variants in gene SMARCC1 reported as likely benign for Inborn genetic diseases

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_003074.4(SMARCC1):c.1252G>A (p.Ala418Thr)
NM_003074.4(SMARCC1):c.3262G>A (p.Ala1088Thr)
NM_003074.4(SMARCC1):c.349G>A (p.Ala117Thr)	rs746514755

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