List of variants in gene SMC1A reported as likely pathogenic by Baylor Genetics

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_006306.4(SMC1A):c.110G>T (p.Gly37Val)	rs1569359540
NM_006306.4(SMC1A):c.128A>T (p.Asp43Val)	rs1569359535
NM_006306.4(SMC1A):c.1546-2A>C	rs2520930904
NM_006306.4(SMC1A):c.3103C>T (p.Arg1035Ter)	rs1556886124
NM_006306.4(SMC1A):c.3196C>A (p.Arg1066Ser)	rs797044896
NM_006306.4(SMC1A):c.586C>T (p.Arg196Cys)	rs587784422

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