ClinVar Miner

List of variants in gene LCAT reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (916):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000229.2(LCAT):c.*12T>C rs886052219
NM_000229.2(LCAT):c.1039C>T (p.Arg347Cys) rs202017590
NM_000229.2(LCAT):c.159C>T (p.Pro53=) rs556480808
NM_000229.2(LCAT):c.534G>T (p.Glu178Asp) rs886052220
NM_000229.2(LCAT):c.748+13C>G rs750086555
NM_000229.2(LCAT):c.981A>C (p.Gly327=) rs139453193

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