ClinVar Miner

List of variants in gene LOC129388752, SLC30A10 studied for Hypermanganesemia with dystonia, polycythemia, and cirrhosis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
nsv1067840

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