List of variants in gene MITF reported as benign by Clinical Genetics, Academic Medical Center

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001354604.2(MITF):c.880+9C>G	rs181810413	0.00203
NM_001354604.2(MITF):c.1569G>A (p.Glu523=)	rs200830148	0.00092
NM_001354604.2(MITF):c.1280T>C (p.Val427Ala)	rs2055006	0.00091
NM_001354604.2(MITF):c.104+24216T>C	rs781087974	0.00001

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