RS121908287 FIG4
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121908287, also known as I41T, is a SNP in the FIG4 gene that encodes a variation for an amino aci...
Associated Conditions
Charcot-Marie-Tooth disease type 4J
Amyotrophic lateral sclerosis type 11
Charcot-Marie-Tooth disease type 4
Amyotrophic lateral sclerosis
Yunis-Varon syndrome
Bilateral parasagittal parieto-occipital polymicrogyria
Inborn genetic diseases
FIG4-related disorder
Charcot-Marie-Tooth disease type 4J
Amyotrophic lateral sclerosis type 11
Charcot-Marie-Tooth disease type 4
Amyotrophic lateral sclerosis
Yunis-Varon syndrome
Bilateral parasagittal parieto-occipital polymicrogyria
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0.2%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
0.3%
1kG EAS
100%
1kG EUR
0.2%
1kG SAS
100%
Other Variants in FIG4