List of variants in gene IHH reported as likely pathogenic for bone development disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002181.4(IHH):c.1A>G (p.Met1Val)
NM_002181.4(IHH):c.352G>A (p.Val118Met)	rs1454141074
NM_002181.4(IHH):c.478C>T (p.Arg160Cys)	rs1948842030

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