List of variants in gene FGD4 reported as pathogenic for not provided

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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.1081C>T (p.Arg361Ter)	rs118203972
NM_001370298.3(FGD4):c.1363_1364del (p.Glu455fs)	rs771606350
NM_001370298.3(FGD4):c.1740C>A (p.Tyr580Ter)	rs886041200
NM_001370298.3(FGD4):c.1808_1809del (p.Thr603fs)	rs886039361
NM_001370298.3(FGD4):c.2141G>A (p.Arg714Gln)	rs372890690
NM_001370298.3(FGD4):c.2298_2302del (p.Lys767fs)	rs751035912
NM_001370298.3(FGD4):c.2298_2302dup (p.Gly768fs)	rs751035912
NM_001370298.3(FGD4):c.875_878del (p.Ser292fs)

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