RS751128300 RPGRIP1L

Health Risk Chr 16:53649068
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What This Variant Does
"CLNSIG=4
Associated Conditions
Meckel-Gruber syndrome
Joubert syndrome
Joubert syndrome and related disorders
Inborn genetic diseases
Meckel-Gruber syndrome
Joubert syndrome
Joubert syndrome and related disorders
Inborn genetic diseases
Other Variants in RPGRIP1L
rs121918197 rs121918198 rs121918199 rs121918200 rs121918201 rs121918202 rs121918203 rs121918204 rs387906243 rs145665129
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