Variant (rsID / SNP)

rs10183087

rs10183087 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ICOS. Location: chromosome 2, position 204,824,324. Clinical significance in the table: Benign.

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Reference-table entries

ICOSBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:204824324
Cytoband: 2q33.2
HGVS: NM_012092.4(ICOS):c.*2A>C
Allele change: Silent

Associated conditions / phenotypes

Immunodeficiency, common variable, 1

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.