RS760300569 HECW2

Health Risk Chr 2:196220808
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Inborn genetic diseases
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Other Variants in HECW2
rs878854416 rs878854422 rs878854417 rs143511416 rs1057524302 rs770779546 rs1553629086 rs774316240 rs1553633403 rs1553635778
Ask Dr. Hemsworth about this variant