List of variants in gene SIN3A reported as likely benign for chromosomal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001145358.2(SIN3A):c.3466A>T (p.Met1156Leu)	rs60213317	0.00716
NM_001145358.2(SIN3A):c.1428T>C (p.Ser476=)	rs58376508	0.00645
NM_001145358.2(SIN3A):c.3653C>G (p.Thr1218Ser)

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