List of variants in gene combination LOC107652445, SHOX reported as uncertain significance 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_000451.4(SHOX):c.374C>G (p.Thr125Arg)
NM_000451.4(SHOX):c.389A>C (p.Asn130Thr)	rs2052712369
NM_000451.4(SHOX):c.463G>T (p.Gly155Trp)	rs765251991

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