RS587777678 LAMA1

Health Risk Chr 18:6956768
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Other Variants in LAMA1
rs587777677 rs587777679 rs587777680 rs587777681 rs773505947 rs797044940 rs797045182 rs797045184 rs769174266 rs147676957
Ask Dr. Hemsworth about this variant