List of variants in gene LRMDA reported as benign for disorder of melanin metabolism

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001305581.2(LRMDA):c.364T>C (p.Leu122=)	rs1898071	0.42882
NM_001305581.2(LRMDA):c.516+53C>T	rs7924288	0.40010
NM_001305581.2(LRMDA):c.398+31A>C	rs1898070	0.37753

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