Variants in gene MERTK with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_006343.3(MERTK):c.102A>G (p.Leu34=)	rs143215350	0.00763
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.231C>T (p.Asn77=)	rs137909193	0.00169
NM_006343.3(MERTK):c.960+9C>A	rs373198570	0.00116
NM_006343.3(MERTK):c.1297-4C>A	rs141641623	0.00009
NM_006343.3(MERTK):c.1340G>A (p.Arg447Gln)	rs753693755	0.00002
NM_006343.3(MERTK):c.1960+8C>T	rs112541306

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