List of variants in gene FGD4 reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.167-29728T>C	rs561223009	0.00065
NM_001370298.3(FGD4):c.1923-7A>G	rs200542541	0.00020
NM_001370298.3(FGD4):c.1973A>G (p.Asp658Gly)	rs141237776	0.00015
NM_001370298.3(FGD4):c.1405-7A>G	rs1948890717	0.00001
NM_001370298.3(FGD4):c.2132C>T (p.Ala711Val)	rs1341534652	0.00001
NM_001370298.3(FGD4):c.1134C>G (p.Asn378Lys)
NM_001370298.3(FGD4):c.1699C>T (p.Leu567Phe)	rs2540705650
NM_001370298.3(FGD4):c.376C>A (p.Pro126Thr)	rs199744649

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