ClinVar Miner

List of variants in gene LRAT reported as likely benign for Leber congenital amaurosis

Included ClinVar conditions (39):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_004744.5(LRAT):c.*1338T>G rs12507608
NM_004744.5(LRAT):c.*1867C>T rs78441257
NM_004744.5(LRAT):c.*2258_*2259insTGTTGTGCTGAGTTT rs372786858
NM_004744.5(LRAT):c.*2670G>T rs17032000
NM_004744.5(LRAT):c.*3618G>A rs17032002
NM_004744.5(LRAT):c.*817A>G rs78274322
NM_004744.5(LRAT):c.342G>A (p.Glu114=) rs17031981

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