ClinVar Miner

List of variants in gene SLC34A3 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_001177316.2(SLC34A3):c.1060G>A (p.Val354Met)	rs534880363	0.00005
NM_001177316.2(SLC34A3):c.632G>A (p.Ser211Asn)	rs760863723

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