List of variants in gene LINS1 reported as benign by Ambry Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001040616.3(LINS1):c.1899C>T (p.Asp633=)	rs12460	0.49059
NM_001040616.3(LINS1):c.1128T>C (p.Ser376=)	rs12592868	0.39066
NM_001040616.3(LINS1):c.1452A>T (p.Thr484=)	rs2411836	0.38324
NM_001040616.3(LINS1):c.660C>T (p.Phe220=)	rs8039437	0.38092
NM_001040616.3(LINS1):c.1923G>C (p.Glu641Asp)	rs12157	0.37874
NM_001040616.3(LINS1):c.2040G>T (p.Arg680Ser)	rs8451	0.37872
NM_001040616.3(LINS1):c.1824G>T (p.Gly608=)	rs6598356	0.37869
NM_001040616.3(LINS1):c.85A>G (p.Ile29Val)	rs11247226	0.36216
NM_001040616.3(LINS1):c.1415G>C (p.Ser472Thr)	rs2411837	0.31881
NM_001040616.3(LINS1):c.1621A>G (p.Ile541Val)	rs12915007	0.03296
NM_001040616.3(LINS1):c.992C>T (p.Ala331Val)	rs34967129	0.02291

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