RS760205035 CSPP1

Health Risk Chr 8:67112065
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Associated Conditions
Joubert syndrome 21
Inborn genetic diseases
Uveal melanoma
Joubert syndrome 21
Inborn genetic diseases
Uveal melanoma
Other Variants in CSPP1
rs587777138 rs587777139 rs587777140 rs587777141 rs587777142 rs587777143 rs375113643 rs1554562278 rs587777145 rs587777146
Ask Dr. Hemsworth about this variant