List of variants in gene SMC1A reported as likely benign for not specified

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006306.4(SMC1A):c.1323C>T (p.Tyr441=)	rs144850468	0.00183
NM_006306.4(SMC1A):c.3450C>T (p.Ala1150=)	rs142611198	0.00183
NM_006306.4(SMC1A):c.2824C>T (p.Leu942=)	rs139654605	0.00039
NM_006306.4(SMC1A):c.1098G>A (p.Thr366=)	rs140585416	0.00015
NM_006306.4(SMC1A):c.298+12T>C	rs782781148	0.00004
NM_006306.4(SMC1A):c.1254+4G>A	rs781824288	0.00002
NM_006306.4(SMC1A):c.3618+7C>T	rs782267492	0.00002
NM_006306.4(SMC1A):c.2191C>T (p.Leu731=)	rs782301753	0.00001
NM_006306.4(SMC1A):c.480T>A (p.Arg160=)	rs782369322	0.00001
NM_006306.4(SMC1A):c.2456T>G (p.Ile819Ser)	rs587784413
NM_006306.4(SMC1A):c.616-6G>A	rs587784424

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