Variant (rsID / SNP)

rs838133

rs838133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGF21, FUT1. Location: chromosome 19, position 49,259,529. The table records no clinical significance for this variant.

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Reference-table entries

FGF21Not classified

Variant type: synonymous_variant
Chromosome / position: 19:49259529
HGVS: NM_019113.4,c.36A>G,p.Gly12Gly
Allele change: Synonymous_G12G

Associated conditions / phenotypes

Alzheimer Disease|Non-Alcoholic Fatty Liver Disease|Fatty Liver Disease

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.