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Variant (rsID / SNP)

rs2241883

FABP1

rs2241883 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FABP1. Location: chromosome 2, position 88,424,066. The table records no clinical significance for this variant.

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Reference-table entries

FABP1Not classified
Variant type
missense_variant
Chromosome / position
2:88424066
HGVS
NM_001443.3,c.280A>G,p.Thr94Ala
Allele change
Missense_T94A

Associated conditions / phenotypes

Polycystic Ovary Syndrome|Lipid Metabolism Disorder|Liver Disease|Non-Alcoholic Fatty Liver Disease|Fatty Liver Disease|Hepatocellular Carcinoma|Liver Cirrhosis|Hypercholesterolemia, Familial, 1|Gallbladder Disease 1|Hypercholesterolemia, Familial, 3|Type 2 Diabetes Mellitus|Diabetes Mellitus

Public references

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