Variant (rsID / SNP)

rs1051266

rs1051266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC19A1. Location: chromosome 21, position 46,957,794. Clinical significance in the table: drug response.

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Reference-table entries

SLC19A1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 21:46957794
Cytoband: 21q22.3
HGVS: NM_194255.4(SLC19A1):c.80A>G (p.His27Arg)
Allele change: Silent

Associated conditions / phenotypes

Gastrointestinal stromal tumor|methotrexate response - Efficacy

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.