RS769644598 LAMA1

Health Risk Chr 18:6958544
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Associated Conditions
Inborn genetic diseases
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Retinal dystrophy
Inborn genetic diseases
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Retinal dystrophy
Other Variants in LAMA1
rs587777677 rs587777678 rs587777679 rs587777680 rs587777681 rs773505947 rs797044940 rs797045182 rs797045184 rs769174266
Ask Dr. Hemsworth about this variant