ClinVar Miner

List of variants in gene ARL13B reported as likely benign for Joubert syndrome 1

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_182896.2(ARL13B):c.*1549T>C rs567211919
NM_182896.2(ARL13B):c.*547C>T rs75280469
NM_182896.2(ARL13B):c.*980A>G rs78386221
NM_182896.2(ARL13B):c.-234G>T rs114936013
NM_182896.2(ARL13B):c.-257C>T rs73846074
NM_182896.2(ARL13B):c.1043C>G (p.Thr348Ser) rs33944211

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