ClinVar Miner

List of variants in gene combination C12orf29, CEP290 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: 7
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HGVS dbSNP
NM_001009894.3(C12orf29):c.*618_*621TATT[1] rs886049876
NM_001009894.3(C12orf29):c.*786A>T rs794727762
NM_001009894.3(C12orf29):c.*807_*808CT[1] rs569673313
NM_001009894.3(C12orf29):c.*827G>A rs754398792
NM_001009894.3(C12orf29):c.*837T>C rs765709669
NM_001009894.3(C12orf29):c.*891C>A rs534440681
NM_001009894.3(C12orf29):c.*926C>T rs200178519

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