RS1057523157 SETD2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Luscan-Lumish syndrome
Corpus callosum
agenesis of
Cerebellar vermis hypoplasia
SETD2-related disorder
Inborn genetic diseases
Congenital cerebellar hypoplasia
Rabin-Pappas syndrome
SETD2 associated neurodevelopmental disorder with multiple congenital anomalies
Luscan-Lumish syndrome
Corpus callosum
agenesis of
Cerebellar vermis hypoplasia
SETD2-related disorder
Inborn genetic diseases
Other Variants in SETD2