List of variants in gene MERTK reported as likely benign for MERTK-related retinopathy

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_006343.3(MERTK):c.2851G>A (p.Ala951Thr)	rs148261231	0.00304
NM_006343.3(MERTK):c.2593C>T (p.Arg865Trp)	rs2230516	0.00274
NM_006343.3(MERTK):c.1493_1494inv (p.Asn498Ser)
NM_006343.3(MERTK):c.669G>A (p.Pro223=)	rs750984679

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