ClinVar Miner

List of variants in gene MARVELD2 reported as pathogenic for obsolete rare genetic deafness

Included ClinVar conditions (7):

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_001038603.3(MARVELD2):c.1498C>T (p.Arg500Ter)	rs118203957	0.00009
NM_001038603.3(MARVELD2):c.1331+1G>A	rs762352115	0.00001

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