List of variants in gene NHLRC1 reported as likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_198586.3(NHLRC1):c.46A>G (p.Met16Val)	rs146636139	0.00108
NM_198586.3(NHLRC1):c.969C>T (p.Ser323=)	rs142941035	0.00022
NM_198586.3(NHLRC1):c.990G>A (p.Gln330=)	rs148553723	0.00021
NM_198586.3(NHLRC1):c.513C>T (p.Ala171=)	rs148907696	0.00013
NM_198586.3(NHLRC1):c.478T>C (p.Cys160Arg)	rs200595273	0.00011
NM_198586.3(NHLRC1):c.1017T>C (p.Ser339=)	rs747655441	0.00003
NM_198586.3(NHLRC1):c.1065G>A (p.Pro355=)	rs752799460	0.00001
NM_198586.3(NHLRC1):c.741G>A (p.Ala247=)	rs571973789	0.00001
NM_198586.3(NHLRC1):c.138C>T (p.Cys46=)	rs1489142985
NM_198586.3(NHLRC1):c.216G>A (p.Arg72=)	rs1561882237
NM_198586.3(NHLRC1):c.372G>C (p.Gly124=)
NM_198586.3(NHLRC1):c.399G>A (p.Ala133=)
NM_198586.3(NHLRC1):c.738C>T (p.Phe246=)	rs1561881781

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