RS116690149 LAMA1

Health Risk Chr 18:7036033 snv missense variant
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Associated Conditions
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Inborn genetic diseases
LAMA1-related disorder
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Inborn genetic diseases
LAMA1-related disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.5%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in LAMA1
rs587777677 rs587777678 rs587777679 rs587777680 rs587777681 rs773505947 rs797044940 rs797045182 rs797045184 rs769174266
Ask Dr. Hemsworth about this variant