ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance by GeneDx

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001370298.3(FGD4):c.740T>C (p.Leu247Pro) rs142609007 0.00033
NM_001370298.3(FGD4):c.890G>A (p.Gly297Asp) rs201826412 0.00024
NM_001370298.3(FGD4):c.1759A>G (p.Met587Val) rs201186597 0.00016
NM_001370298.3(FGD4):c.1973A>G (p.Asp658Gly) rs141237776 0.00015
NM_001370298.3(FGD4):c.1142C>T (p.Ser381Leu) rs201915829 0.00011
NM_001370298.3(FGD4):c.2123C>A (p.Pro708His) rs145071617 0.00010
NM_001370298.3(FGD4):c.792A>G (p.Ile264Met) rs774466701 0.00006
NM_001370298.3(FGD4):c.980T>A (p.Leu327Gln) rs144980336 0.00006
NM_001370298.3(FGD4):c.461C>G (p.Pro154Arg) rs371407163 0.00003
NM_001370298.3(FGD4):c.895G>C (p.Gly299Arg) rs774679169 0.00003
NM_001370298.3(FGD4):c.1366C>T (p.Arg456Cys) rs1131691854 0.00001
NM_001370298.3(FGD4):c.1614G>C (p.Lys538Asn) rs1131691394 0.00001
NM_001370298.3(FGD4):c.319+1G>A rs1057518446 0.00001
NM_001370298.3(FGD4):c.556G>C (p.Ala186Pro) rs754942816 0.00001
NM_001370298.3(FGD4):c.789C>G (p.His263Gln) rs757469397 0.00001
NM_001370298.3(FGD4):c.949G>A (p.Glu317Lys) rs148406003 0.00001
NM_001370298.3(FGD4):c.1689A>C (p.Glu563Asp) rs879254000
NM_001370298.3(FGD4):c.1715G>A (p.Arg572Gln)
NM_001370298.3(FGD4):c.2122C>G (p.Pro708Ala) rs144693221
NM_001370298.3(FGD4):c.2313G>A (p.Glu771=)
NM_001370298.3(FGD4):c.2560G>T (p.Val854Leu) rs61753359

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