RS869312821 GNB1

Health Risk Chr 1:1806515
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What This Variant Does
"CLNSIG=5
Associated Conditions
Global developmental delay
Intellectual disability
Hypotonia
Floppy infant
Acute lymphoid leukemia
autosomal dominant 42
Neurodevelopmental Disability
Seizure
Global developmental delay
Intellectual disability
Hypotonia
Floppy infant
Acute lymphoid leukemia
autosomal dominant 42
Neurodevelopmental Disability
Other Variants in GNB1
rs752746786 rs869312826 rs869312825 rs869312824 rs869312823 rs758432471 rs869312822 rs1064795844 rs1135401746 rs771603036
Ask Dr. Hemsworth about this variant