RS782397980 CHAMP1;LINC01054

Health Risk Chr 13:114325331

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What This Variant Does

"CLNSIG=5

Associated Conditions

Intellectual disability

autosomal dominant 40

Inborn genetic diseases

CHAMP1-related syndrome

Intellectual disability

autosomal dominant 40

Inborn genetic diseases

CHAMP1-related syndrome

Ask Dr. Hemsworth about this variant