RS137852521 L1CAM

Health Risk Chr X:153870933
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
X-linked hydrocephalus syndrome
L1 syndrome
Inborn genetic diseases
Spastic paraplegia
X-linked hydrocephalus syndrome
L1 syndrome
Inborn genetic diseases
Spastic paraplegia
Other Variants in L1CAM
rs879253713 rs137852518 rs28933683 rs137852519 rs137852520 rs879253714 rs137852522 rs137852523 rs137852524 rs879253715
Ask Dr. Hemsworth about this variant