Variant (rsID / SNP)

rs2228145

rs2228145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL6R. Location: chromosome 1, position 154,426,970. Clinical significance in the table: Benign.

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Reference-table entries

IL6RBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:154426970
Cytoband: 1q21.3
HGVS: NM_000565.4(IL6R):c.1073A>C (p.Asp358Ala)
Allele change: Missense_D358A

Associated conditions / phenotypes

Soluble interleukin-6 receptor, serum level of, quantitative trait locus|Interleukin 6, serum level of, quantitative trait locus

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.