RS886039400 KRIT1
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What This Variant Does
"aka c.152_155delAAGT (p.Lys51Ilefs)
Associated Conditions
Cerebral cavernous malformation
Hereditary cavernous hemangioma of brain
KRIT1-related disorder
Inborn genetic diseases
Cerebral cavernous malformation
Hereditary cavernous hemangioma of brain
KRIT1-related disorder
Inborn genetic diseases
Other Variants in KRIT1