ClinVar Miner

List of variants in gene SIN3A 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001145358.2(SIN3A):c.942C>T (p.Ile314=)	rs147885320	0.00096
NM_001145358.2(SIN3A):c.3438A>G (p.Glu1146=)	rs372034400	0.00020

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