RS752176040 TMCO1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Craniofacial dysmorphism
skeletal anomalies
and impaired intellectual development 1
Inborn genetic diseases
TMCO1-related disorder
Craniofacial dysmorphism
skeletal anomalies
and impaired intellectual development 1
Inborn genetic diseases
TMCO1-related disorder
Other Variants in TMCO1