List of variants in gene NHS reported as benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001291867.2(NHS):c.211C>T (p.Pro71Ser)	rs398124605	0.03116
NM_001291867.2(NHS):c.2831A>T (p.His944Leu)	rs149244552	0.00386
NM_001291867.2(NHS):c.3545C>T (p.Pro1182Leu)	rs145977627	0.00189
NM_001291867.2(NHS):c.4168G>A (p.Asp1390Asn)	rs142186771	0.00081
NM_001291867.2(NHS):c.3929G>T (p.Gly1310Val)	rs41304731	0.00074
NM_001291867.2(NHS):c.766C>G (p.Leu256Val)	rs200598087	0.00009
NM_001291867.2(NHS):c.207GCC[3] (p.Pro73del)	rs10590816
NM_001291867.2(NHS):c.310_345del (p.Pro104_Ala115del)	rs797045741

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