List of variants in gene NHS reported as uncertain significance 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001291867.2(NHS):c.765C>G (p.Pro255=)	rs143119491	0.00086
NM_001291867.2(NHS):c.1603G>A (p.Val535Met)	rs367856134	0.00028
NM_001291867.2(NHS):c.513C>T (p.Leu171=)	rs398124610	0.00028
NM_001291867.2(NHS):c.1143C>T (p.Cys381=)	rs727504042	0.00012
NM_001291867.2(NHS):c.3408G>A (p.Thr1136=)	rs370811549	0.00009
NM_001291867.2(NHS):c.1175G>A (p.Arg392Gln)	rs372969054	0.00007
NM_001291867.2(NHS):c.1327G>A (p.Gly443Arg)	rs371229391	0.00006
NM_001291867.2(NHS):c.152C>T (p.Ala51Val)	rs727504039	0.00005
NM_001291867.2(NHS):c.3515C>T (p.Thr1172Met)	rs149099378	0.00005
NM_001291867.2(NHS):c.618G>A (p.Pro206=)	rs200952266	0.00005
NM_001291867.2(NHS):c.827A>G (p.Glu276Gly)	rs886042656	0.00005
NM_001291867.2(NHS):c.4860G>C (p.Arg1620=)	rs761212213	0.00003
NM_001291867.2(NHS):c.1155T>C (p.His385=)	rs727504043	0.00002
NM_001291867.2(NHS):c.1998G>A (p.Glu666=)	rs1278511688	0.00002
NM_001291867.2(NHS):c.2234C>T (p.Ala745Val)	rs139037690	0.00002
NM_001291867.2(NHS):c.2348G>A (p.Gly783Glu)	rs398124606	0.00002
NM_001291867.2(NHS):c.2921T>C (p.Val974Ala)	rs747843383	0.00001
NM_001291867.2(NHS):c.3891C>T (p.Asp1297=)	rs761463158	0.00001
NM_001291867.2(NHS):c.49C>T (p.Arg17Trp)	rs794726963	0.00001
NM_001291867.2(NHS):c.660A>C (p.Pro220=)	rs794727314	0.00001
NM_001291867.2(NHS):c.1108G>A (p.Gly370Arg)	rs727504041
NM_001291867.2(NHS):c.147C>T (p.Val49=)	rs794726961
NM_001291867.2(NHS):c.302_337dup (p.Glu101_Ala112dup)	rs398124607
NM_001291867.2(NHS):c.401G>A (p.Arg134His)	rs794726962
NM_001291867.2(NHS):c.4428_4430dup (p.Ser1480dup)	rs398124609
NM_001291867.2(NHS):c.4783A>C (p.Thr1595Pro)	rs794727936
NM_001291867.2(NHS):c.565+7A>C	rs794726960

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