RS151279194 CPLANE1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Joubert syndrome 17
See cases
Orofaciodigital syndrome type 6
CPLANE1-related disorder
Inborn genetic diseases
Joubert syndrome 17
See cases
Orofaciodigital syndrome type 6
CPLANE1-related disorder
Inborn genetic diseases
Other Variants in CPLANE1