ClinVar Miner

List of variants in gene CYP4V2 reported as uncertain significance for Corneal Dystrophy, Recessive

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Total variants: 21
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HGVS dbSNP
NM_207352.3(CYP4V2):c.-302G>A rs549805175
NM_207352.4(CYP4V2):c.*1023_*1024del rs886059287
NM_207352.4(CYP4V2):c.*1023_*1026del rs886059286
NM_207352.4(CYP4V2):c.*1025_*1026CA[18] rs60425964
NM_207352.4(CYP4V2):c.*1025_*1026CA[19] rs60425964
NM_207352.4(CYP4V2):c.*1054_*1055insTA rs144125100
NM_207352.4(CYP4V2):c.*1056_*1057insCACACATACA rs1554075269
NM_207352.4(CYP4V2):c.*1056_*1057insCATACA rs1554075269
NM_207352.4(CYP4V2):c.*1057delinsCACACACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACACACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACACACACACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACACACACACACACACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACACACACACACACACACATACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACACACATACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACACATACAC rs869178465
NM_207352.4(CYP4V2):c.*1057delinsCACATACAC rs869178465
NM_207352.4(CYP4V2):c.*1059_*1060CA[5] rs58524374
NM_207352.4(CYP4V2):c.*1123_*1127del rs574084304
NM_207352.4(CYP4V2):c.*1967C>T rs886059294
NM_207352.4(CYP4V2):c.311A>G (p.Asn104Ser) rs886059281
NM_207352.4(CYP4V2):c.802-8_810delinsGC rs207482233

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