List of variants in gene SMC3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_005445.4(SMC3):c.92-19A>G	rs140102981	0.00310
NM_005445.4(SMC3):c.255A>G (p.Ser85=)	rs146433240	0.00287
NM_005445.4(SMC3):c.2329T>C (p.Leu777=)	rs76625999	0.00132
NM_005445.4(SMC3):c.3495T>A (p.Ala1165=)	rs142395521	0.00064
NM_005445.4(SMC3):c.1280A>G (p.Lys427Arg)	rs142524280	0.00057
NM_005445.4(SMC3):c.837A>G (p.Thr279=)	rs151335692	0.00018
NM_005445.4(SMC3):c.2062G>C (p.Glu688Gln)	rs201162818	0.00013
NM_005445.4(SMC3):c.2782C>A (p.Arg928=)	rs202034783	0.00011
NM_005445.4(SMC3):c.2493T>C (p.Tyr831=)	rs112525060	0.00007
NM_005445.4(SMC3):c.2982C>T (p.Ser994=)	rs201308737	0.00003
NM_005445.4(SMC3):c.1410-30_1410-25del	rs147070453
NM_005445.4(SMC3):c.1410-6_1410-3del	rs546049291
NM_005445.4(SMC3):c.1647C>T (p.Cys549=)
NM_005445.4(SMC3):c.198+3G>A	rs533706811
NM_005445.4(SMC3):c.270+8A>G
NM_005445.4(SMC3):c.3298-3dup	rs750133429
NM_005445.4(SMC3):c.588T>C (p.Ile196=)
NM_005445.4(SMC3):c.714A>G (p.Lys238=)
NM_005445.4(SMC3):c.867A>G (p.Glu289=)
NM_005445.4(SMC3):c.951A>T (p.Ala317=)

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