ClinVar Miner

List of variants in gene PAPSS1 reported as uncertain significance by Undiagnosed Diseases Network, NIH

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_005443.5(PAPSS1):c.331C>T (p.Arg111Ter)	rs142366340	0.00035
NM_005443.5(PAPSS1):c.286A>G (p.Asn96Asp)	rs2530212591

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