List of variants in gene NHERF1 reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004252.5(NHERF1):c.458G>A (p.Arg153Gln)	rs41282065	0.00267
NM_004252.5(NHERF1):c.555C>A (p.Asp185Glu)	rs200926419	0.00109
NM_004252.5(NHERF1):c.888+2T>C	rs138547261	0.00022
NM_004252.5(NHERF1):c.609C>T (p.Asn203=)
NM_004252.5(NHERF1):c.758-3T>C

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