ClinVar Miner

List of variants in gene combination NOC3L, PLCE1 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: 9
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HGVS dbSNP
NM_016341.3(PLCE1):c.[6093T>C;6800G>A]
NM_016341.4(PLCE1):c.*116T>C rs886047506
NM_016341.4(PLCE1):c.*219C>G rs376587612
NM_016341.4(PLCE1):c.*220T>G rs184484950
NM_016341.4(PLCE1):c.*268T>C rs146319051
NM_016341.4(PLCE1):c.*390A>G rs886047507
NM_016341.4(PLCE1):c.6364G>A (p.Val2122Ile) rs528942664
NM_016341.4(PLCE1):c.6377_6378del (p.Lys2126fs) rs773902333
NM_016341.4(PLCE1):c.6720+10A>G rs752683058

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