RS587777329 SETD5
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Inborn genetic diseases
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Inborn genetic diseases
Other Variants in SETD5