ClinVar Miner

List of variants in gene MITF reported as uncertain significance by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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_001354604.2(MITF):c.881-7T>A	rs200580325	0.00041
NM_001354604.2(MITF):c.329C>T (p.Thr110Met)	rs190215588	0.00019

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