RS587777621 CCND2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3
Inborn genetic diseases
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3
Inborn genetic diseases
Other Variants in CCND2