ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000276.4(OCRL):c.1367A>C (p.Gln456Pro) rs1569460215
NM_000276.4(OCRL):c.1370G>C (p.Arg457Pro)
NM_000276.4(OCRL):c.1467-3C>G
NM_000276.4(OCRL):c.1514G>A (p.Gly505Glu) rs1569460717
NM_000276.4(OCRL):c.1602G>A (p.Gly534=) rs773214157
NM_000276.4(OCRL):c.2635C>T (p.Gln879Ter) rs1556359544
NM_000276.4(OCRL):c.40-5C>T rs201211377
NM_000276.4(OCRL):c.746T>G (p.Val249Gly)

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