ClinVar Miner

List of variants in gene combination MVP-DT, PRRT2 reported by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_145239.3(PRRT2):c.125C>T (p.Pro42Leu)	rs1166053009	0.00001
NM_145239.3(PRRT2):c.173C>G (p.Pro58Arg)	rs1567378768

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