RS387906309 HEXA

Health Risk Chr 15:72346579
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What This Variant Does
"rs387906309, also known as c.1274_1277dupTATC or p.Tyr427Ilefs, is a rare variant in the HEXA gene o...
Associated Conditions
Tay-Sachs disease
Inborn genetic diseases
Intellectual disability
variant AB
HEXA-related disorder
Tay-Sachs disease
Inborn genetic diseases
Intellectual disability
variant AB
HEXA-related disorder
Other Variants in HEXA
rs147324677 rs121907952 rs797044432 rs797044433 rs121907955 rs28941770 rs121907953 rs121907954 rs121907956 rs121907957
Ask Dr. Hemsworth about this variant