RS775951098 CC2D1A

Health Risk Chr 19:13906496
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CC2D1A
rs541952457 rs201177183 rs202057391 rs534160840 rs201374643 rs191830054 rs143529486 rs201884654 rs201251295 rs201665826
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