List of variants in gene IVD reported as uncertain significance by Natera, Inc.

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_002225.5(IVD):c.164A>T (p.Lys55Met)	rs145999491	0.00093
NM_002225.5(IVD):c.408G>C (p.Gln136His)	rs569537063	0.00021
NM_002225.5(IVD):c.490A>G (p.Met164Val)	rs574434706	0.00006
NM_002225.5(IVD):c.832A>C (p.Ser278Arg)	rs552272986	0.00005
NM_002225.5(IVD):c.1243G>A (p.Gly415Ser)	rs150855952	0.00004
NM_002225.5(IVD):c.52C>T (p.Arg18Trp)	rs375138989	0.00004
NM_002225.5(IVD):c.1001T>C (p.Met334Thr)	rs368041528	0.00003
NM_002225.5(IVD):c.264C>T (p.Gly88=)	rs377199313	0.00003
NM_002225.5(IVD):c.334A>T (p.Met112Leu)	rs772021923	0.00003
NM_002225.5(IVD):c.895C>G (p.Leu299Val)	rs149247895	0.00003
NM_002225.5(IVD):c.268T>A (p.Leu90Met)	rs780854004	0.00002
NM_002225.5(IVD):c.357C>T (p.Ser119=)	rs776924775	0.00002
NM_002225.5(IVD):c.865G>A (p.Gly289Arg)	rs568885234	0.00002
NM_002225.5(IVD):c.1010G>A (p.Arg337Gln)	rs139908696	0.00001
NM_002225.5(IVD):c.1160A>G (p.Asp387Gly)	rs1163816425	0.00001
NM_002225.5(IVD):c.202A>G (p.Ile68Val)	rs758926864	0.00001
NM_002225.5(IVD):c.307C>G (p.Leu103Val)	rs1465206137	0.00001
NM_002225.5(IVD):c.456G>A (p.Lys152=)	rs886044117	0.00001
NM_002225.5(IVD):c.539C>T (p.Ala180Val)	rs559732306	0.00001
NM_002225.5(IVD):c.710C>T (p.Ser237Phe)	rs1891244554	0.00001
NM_002225.5(IVD):c.784+9C>T	rs1891254953	0.00001
NM_002225.5(IVD):c.796C>G (p.Leu266Val)	rs766980574	0.00001
NM_002225.5(IVD):c.803A>G (p.His268Arg)	rs201778625	0.00001
NM_002225.5(IVD):c.1136T>C (p.Phe379Ser)	rs1469021843
NM_002225.5(IVD):c.137A>G (p.Gln46Arg)	rs1890355492
NM_002225.5(IVD):c.148C>G (p.Arg50Gly)	rs34695403
NM_002225.5(IVD):c.17G>A (p.Arg6Gln)	rs748160492
NM_002225.5(IVD):c.233G>C (p.Arg78Pro)	rs771929559
NM_002225.5(IVD):c.438A>G (p.Lys146=)	rs1007239169
NM_002225.5(IVD):c.467G>C (p.Gly156Ala)	rs1221254988
NM_002225.5(IVD):c.60G>T (p.Pro20=)	rs1482549847
NM_002225.5(IVD):c.823G>A (p.Val275Met)	rs757832700
NM_002225.5(IVD):c.848A>G (p.Glu283Gly)	rs1314850102
NM_002225.5(IVD):c.865G>T (p.Gly289Trp)	rs568885234
NM_002225.5(IVD):c.870G>T (p.Gly290=)	rs1285915480
NM_002225.5(IVD):c.995G>T (p.Arg332Leu)	rs745464766

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