List of variants in gene IVD reported as uncertain significance by Counsyl

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002225.5(IVD):c.707C>T (p.Thr236Ile)	rs146861563	0.00010
NM_002225.5(IVD):c.1232G>A (p.Arg411Gln)	rs143348838	0.00004
NM_002225.5(IVD):c.851G>A (p.Arg284Gln)	rs373534546	0.00003
NM_002225.5(IVD):c.596G>T (p.Gly199Val)	rs121434285	0.00002
NM_002225.5(IVD):c.1139-3C>G	rs367891946	0.00001
NM_002225.5(IVD):c.1184G>A (p.Arg395Gln)	rs1477527791	0.00001
NM_002225.5(IVD):c.1205T>C (p.Ile402Thr)	rs763422682	0.00001
NM_002225.5(IVD):c.436A>G (p.Lys146Glu)	rs1448656950	0.00001
NM_002225.5(IVD):c.-8T>G	rs566691073
NM_002225.5(IVD):c.272G>A (p.Gly91Asp)	rs1555403365
NM_002225.5(IVD):c.712AAG[1] (p.Lys239del)	rs1555404430
NM_002225.5(IVD):c.875T>C (p.Leu292Pro)	rs1555404843

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