ClinVar Miner

List of variants in gene SMC1A reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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_006306.4(SMC1A):c.1546-5C>T	rs1556889651	0.00002
NM_006306.4(SMC1A):c.171G>C (p.Arg57=)
NM_006306.4(SMC1A):c.412-9C>T	rs2075720879

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