List of variants in gene FGD4 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=)	rs61748364	0.00526
NM_001370298.3(FGD4):c.*2487C>A	rs188600194	0.00503
NM_001370298.3(FGD4):c.1777C>A (p.Pro593Thr)	rs138160928	0.00168
NM_001370298.3(FGD4):c.666A>T (p.Ala222=)	rs139357821	0.00161
NM_001370298.3(FGD4):c.890G>A (p.Gly297Asp)	rs201826412	0.00024
NM_001370298.3(FGD4):c.1194T>C (p.Asn398=)	rs201678865	0.00001
NM_001370298.3(FGD4):c.2616C>T (p.Ile872=)	rs759982135	0.00001
NM_001370298.3(FGD4):c.1098T>C (p.Asp366=)
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)	rs144693221
NM_001370298.3(FGD4):c.805A>C (p.Arg269=)

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