RS886041593 SETD5
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
See cases
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Intellectual disability
Inborn genetic diseases
See cases
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Intellectual disability
Other Variants in SETD5