List of variants in gene NHERF1 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_004252.5(NHERF1):c.627G>A (p.Gly209=)	rs41282067	0.00490
NM_004252.5(NHERF1):c.673G>A (p.Glu225Lys)	rs119486097	0.00351
NM_004252.5(NHERF1):c.902A>T (p.Asp301Val)	rs141613848	0.00124

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