List of variants in gene SMARCA4 reported as uncertain significance by New York Genome Center

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.4876G>A (p.Val1626Met)	rs757412819	0.00001
NM_003072.5(SMARCA4):c.731C>T (p.Pro244Leu)	rs587778683	0.00001
NM_003072.5(SMARCA4):c.3383-36C>T	rs2146595699
NM_003072.5(SMARCA4):c.3557C>T (p.Ala1186Val)	rs1600388982
NM_003072.5(SMARCA4):c.4732G>C (p.Glu1578Gln)	rs1555795999

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