RS778533826 RPGRIP1L

Health Risk Chr 16:53619112
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Joubert syndrome 7
Joubert syndrome
Meckel-Gruber syndrome
Inborn genetic diseases
Meckel syndrome
type 5
COACH syndrome 3
RPGRIP1L-related disorder
Joubert syndrome 7
Joubert syndrome
Meckel-Gruber syndrome
Inborn genetic diseases
Meckel syndrome
type 5
COACH syndrome 3
Other Variants in RPGRIP1L
rs121918197 rs121918198 rs121918199 rs121918200 rs121918201 rs121918202 rs121918203 rs121918204 rs387906243 rs145665129
Ask Dr. Hemsworth about this variant