List of variants in gene SRCAP reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006662.3(SRCAP):c.4603C>G (p.Pro1535Ala)	rs117804715	0.00599
NM_006662.3(SRCAP):c.132C>T (p.Gly44=)	rs149628651	0.00180
NM_006662.3(SRCAP):c.8755C>T (p.Leu2919Phe)	rs149217909	0.00130
NM_006662.3(SRCAP):c.5303T>C (p.Leu1768Pro)	rs587784443	0.00004
NM_006662.3(SRCAP):c.8455A>G (p.Thr2819Ala)	rs779992354	0.00004
NM_006662.3(SRCAP):c.5300C>T (p.Thr1767Met)	rs181491375	0.00003

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