ClinVar Miner

List of variants in gene SMARCA2 reported by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003070.5(SMARCA2):c.3768G>T (p.Met1256Ile)	rs370403102
NM_003070.5(SMARCA2):c.4045C>T (p.Arg1349Ter)
NM_003070.5(SMARCA2):c.67C>T (p.Pro23Ser)

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