ClinVar Miner

List of variants in gene CEP41 reported as benign for Joubert syndrome 1

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_018718.3(CEP41):c.*3526dup rs3839655
NM_018718.3(CEP41):c.*4295G>C rs4728195
NM_018718.3(CEP41):c.*5102G>A rs1990790
NM_018718.3(CEP41):c.-5A>C rs2287371

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