RS104894928 RS1

Health Risk Chr X:18647303
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What This Variant Does
"[OMIM:?]
Associated Conditions
Juvenile retinoschisis
Retinal dystrophy
Inborn genetic diseases
Juvenile retinoschisis
Retinal dystrophy
Juvenile retinoschisis
Retinal dystrophy
Inborn genetic diseases
Juvenile retinoschisis
Retinal dystrophy
Other Variants in RS1
rs61752063 rs61752067 rs104894932 rs104894933 rs104894934 rs104894929 rs104894930 rs61752068 rs199469696 rs199469697
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