List of variants in gene SHOX reported as benign for SHOX-related disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006883.2(SHOX):c.657G>A (p.Pro219=)	rs28474801	0.70636
NM_006883.2(SHOX):c.-512C>A	rs113313554	0.02703
NM_006883.2(SHOX):c.653G>A (p.Arg218His)	rs193072890	0.01306
NM_006883.2(SHOX):c.-636del	rs55872554
NM_006883.2(SHOX):c.-636dup	rs55872554

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