List of variants in gene PIAS3 reported as likely benign for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006099.3(PIAS3):c.1036C>T (p.Leu346=)	rs114124194	0.00463
NM_006099.3(PIAS3):c.105C>T (p.His35=)	rs143409313	0.00164
NM_006099.3(PIAS3):c.1335C>G (p.Val445=)	rs781828952

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