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Variant (rsID / SNP)

rs683369

SLC22A1

rs683369 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A1. Location: chromosome 6, position 160,551,204. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A1Not classified
Variant type
missense_variant
Chromosome / position
6:160551204
HGVS
NM_003057.3,c.480G>C,p.Leu160Phe
Allele change
Missense_L160F

Associated conditions / phenotypes

Leukemia, Chronic Myeloid|Myeloid Leukemia|Primary Biliary Cholangitis|Biliary Cirrhosis, Primary, 1|Liver Cirrhosis|Leukemia|Polycystic Ovary Syndrome|Gastrointestinal Stromal Tumor|Esophageal Cancer|Toxic Shock Syndrome

Public references

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