RS371662397 TCTN2

Health Risk Chr 12:123673618
Upload your DNA to see your genotype for this variant.
Associated Conditions
Meckel-Gruber syndrome
Joubert syndrome
Meckel syndrome
type 8
Joubert syndrome 24
Inborn genetic diseases
Meckel-Gruber syndrome
Joubert syndrome
Meckel syndrome
type 8
Joubert syndrome 24
Inborn genetic diseases
Other Variants in TCTN2
rs374349989 rs79251326 rs786204788 rs786205622 rs141768405 rs188417716 rs149430216 rs147485641 rs144567556 rs797046040
Ask Dr. Hemsworth about this variant