List of variants in gene NHS reported as likely benign by Eurofins NTD LLC (GA)

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001291867.2(NHS):c.2593G>A (p.Ala865Thr)	rs149609550	0.00131
NM_001291867.2(NHS):c.828G>A (p.Glu276=)	rs147497359	0.00096
NM_001291867.2(NHS):c.2330T>C (p.Phe777Ser)	rs143081492	0.00089
NM_001291867.2(NHS):c.4832G>C (p.Ser1611Thr)	rs140651691	0.00086
NM_001291867.2(NHS):c.3929G>T (p.Gly1310Val)	rs41304731	0.00074
NM_001291867.2(NHS):c.1965T>G (p.Pro655=)	rs151009077	0.00069
NM_001291867.2(NHS):c.666C>T (p.Cys222=)	rs138104885	0.00055

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