ClinVar Miner

List of variants in gene PIAS3 reported as benign

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006099.3(PIAS3):c.552T>C (p.Cys184=)	rs112106951	0.01135
NM_006099.3(PIAS3):c.1783A>C (p.Ser595Arg)	rs112103191	0.00077

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