List of variants in gene IVD 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002225.5(IVD):c.1183C>G (p.Arg395Gly)	rs398123681	0.00003
NM_002225.5(IVD):c.1010G>A (p.Arg337Gln)	rs139908696	0.00001
NM_002225.5(IVD):c.456G>A (p.Lys152=)	rs886044117	0.00001
NM_002225.5(IVD):c.726G>C (p.Lys242Asn)	rs794727857	0.00001
NM_002225.5(IVD):c.1066G>A (p.Asp356Asn)	rs398123679
NM_002225.5(IVD):c.785-20A>G	rs727503970
NM_002225.5(IVD):c.863C>T (p.Ala288Val)	rs886042098

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