ClinVar Miner

List of variants in gene SLC30A10 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_018713.3(SLC30A10):c.137C>A (p.Ser46Tyr)	rs2527885316

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