List of variants in gene IHH reported as uncertain significance by GeneDx

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_002181.4(IHH):c.857C>T (p.Pro286Leu)	rs140093604	0.00082
NM_002181.4(IHH):c.1169G>A (p.Arg390His)	rs150661368	0.00054
NM_002181.4(IHH):c.647C>T (p.Ala216Val)	rs142245478	0.00018
NM_002181.4(IHH):c.650G>A (p.Arg217His)	rs145192358	0.00016
NM_002181.4(IHH):c.872G>A (p.Arg291Gln)	rs370408334	0.00013
NM_002181.4(IHH):c.925G>A (p.Val309Met)	rs759546196	0.00003
NM_002181.4(IHH):c.-5del
NM_002181.4(IHH):c.1091del (p.Leu364fs)	rs2106306966
NM_002181.4(IHH):c.1151A>G (p.Tyr384Cys)	rs2106306909
NM_002181.4(IHH):c.228_229delinsAA (p.Arg77Ser)	rs886043368
NM_002181.4(IHH):c.531G>A (p.Trp177Ter)	rs2469514103
NM_002181.4(IHH):c.545_546insTTT (p.Ser182_Lys183insLeu)	rs2469514044
NM_002181.4(IHH):c.893T>G (p.Val298Gly)
NM_002181.4(IHH):c.89C>T (p.Pro30Leu)	rs1948870385
NM_002181.4(IHH):c.949G>A (p.Val317Met)	rs886044074

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