List of variants in gene NHERF1 reported as 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004252.5(NHERF1):c.673G>A (p.Glu225Lys)	rs119486097	0.00351
NM_004252.5(NHERF1):c.458G>A (p.Arg153Gln)	rs41282065	0.00267

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