Variant (rsID / SNP)

rs1617640

rs1617640 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPO. Location: chromosome 7, position 100,317,298. Clinical significance in the table: risk factor.

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Reference-table entries

EPORisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 7:100317298
Cytoband: 7q22.1
HGVS: NM_000799.3(EPO):c.-1306C>A

Associated conditions / phenotypes

Microvascular complications of diabetes, susceptibility to, 2

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.