List of variants in gene FGD4 reported as not provided for Charcot-Marie-Tooth disease type 4H

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.2506A>G (p.Met836Val)	rs140220443	0.00013
NM_001370298.3(FGD4):c.1586G>A (p.Ser529Asn)	rs781528826	0.00004
NM_001370298.3(FGD4):c.1234C>T (p.Arg412Ter)	rs118203974	0.00001
NM_001370298.3(FGD4):c.1304T>C (p.Met435Thr)	rs63749871
NM_001370298.3(FGD4):c.1304T>G (p.Met435Arg)	rs63749871
NM_001370298.3(FGD4):c.1736G>A (p.Arg579His)	rs281865063
NM_001370298.3(FGD4):c.2109G>H (p.Met703Ile)	rs281865064
NM_001370298.3(FGD4):c.2173-2A>G	rs281865065

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