RS139716832 FAT4

Health Risk Chr 4:125408665 snv missense variant
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
100%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
0.1%
1kG SAS
100%
Other Variants in FAT4
rs398122953 rs398122954 rs398122955 rs370088878 rs398122956 rs398122957 rs587777724 rs587777725 rs587777726 rs200221425
Ask Dr. Hemsworth about this variant