RS1209593787 RPGRIP1L

Health Risk Chr 16:53687947
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Associated Conditions
Meckel-Gruber syndrome
Joubert syndrome
Inborn genetic diseases
Meckel-Gruber syndrome
Joubert syndrome
Inborn genetic diseases
Other Variants in RPGRIP1L
rs121918197 rs121918198 rs121918199 rs121918200 rs121918201 rs121918202 rs121918203 rs121918204 rs387906243 rs145665129
Ask Dr. Hemsworth about this variant