List of variants in gene MERTK reported as benign for not specified

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006343.3(MERTK):c.353G>A (p.Ser118Asn)	rs13027171	0.20460
NM_006343.3(MERTK):c.2608G>A (p.Val870Ile)	rs2230517	0.08379
NM_006343.3(MERTK):c.2916G>A (p.Ser972=)	rs10205793	0.06012
NM_006343.3(MERTK):c.61+19G>A	rs115821982	0.03962
NM_006343.3(MERTK):c.60A>T (p.Arg20Ser)	rs35898499	0.03355
NM_006343.3(MERTK):c.102A>G (p.Leu34=)	rs143215350	0.00763
NM_006343.3(MERTK):c.1353A>G (p.Gln451=)	rs35981104	0.00693
NM_006343.3(MERTK):c.2851G>A (p.Ala951Thr)	rs148261231	0.00304
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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