ClinVar Miner

List of variants in gene SLC52A3 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
NC_000020.11:g.759188G>A	rs544939272	0.00113
NM_033409.4(SLC52A3):c.-52+394T>C	rs750886042	0.00004

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