Variant (rsID / SNP)

rs4673993

rs4673993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATIC. Location: chromosome 2, position 216,212,339. Clinical significance in the table: drug response.

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Reference-table entries

ATICDrug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 2:216212339
Cytoband: 2q35
HGVS: NM_004044.7(ATIC):c.1503+675T>C
Allele change: Silent

Associated conditions / phenotypes

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.