List of variants in gene SRCAP 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006662.3(SRCAP):c.493-20C>T	rs72793372	0.15242
NM_006662.3(SRCAP):c.4603C>G (p.Pro1535Ala)	rs117804715	0.00599
NM_006662.3(SRCAP):c.5705A>G (p.Glu1902Gly)	rs117480926	0.00402
NM_006662.3(SRCAP):c.3388C>T (p.Pro1130Ser)	rs143519723	0.00290
NM_006662.3(SRCAP):c.7121C>A (p.Thr2374Asn)	rs142242633	0.00093
NM_006662.3(SRCAP):c.3532C>T (p.Arg1178Cys)	rs200261271	0.00019
NM_006662.3(SRCAP):c.2760C>T (p.Gly920=)	rs527275720	0.00006

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