List of variants in gene SMC3 reported as 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005445.4(SMC3):c.3039A>G (p.Ser1013=)	rs2419565	0.98861
NM_005445.4(SMC3):c.2116+23G>A	rs7075340	0.96693
NM_005445.4(SMC3):c.350+21T>A	rs11195194	0.11880
NM_005445.4(SMC3):c.2644+48A>G	rs11195213	0.11786
NM_005445.4(SMC3):c.970-8G>A	rs11195199	0.11151
NM_005445.4(SMC3):c.1092-18T>C	rs11195200	0.11131
NM_005445.4(SMC3):c.548-45A>C	rs2275570	0.11128
NM_005445.4(SMC3):c.351-9T>C	rs78663177	0.06159
NM_005445.4(SMC3):c.1365T>C (p.Tyr455=)	rs75323904	0.06157
NM_005445.4(SMC3):c.1410-48T>C	rs3737293	0.06060
NM_005445.4(SMC3):c.2007T>C (p.Tyr669=)	rs147404470	0.00501
NM_005445.4(SMC3):c.548-5_548-4dup	rs199906378
NM_005445.4(SMC3):c.724-6dup	rs11380915

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