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rs10183087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10183087(A;C)
Make rs10183087(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position203959601
GeneICOS
is asnp
is mentioned by
dbSNPrs10183087
dbSNP (old)rs10183087
ClinGenrs10183087
ebirs10183087
HLIrs10183087
Exacrs10183087
Gnomadrs10183087
Varsomers10183087
Maprs10183087
PheGenIrs10183087
Biobankrs10183087
1000 genomesrs10183087
hgdprs10183087
ensemblrs10183087
gopubmedrs10183087
geneviewrs10183087
scholarrs10183087
googlers10183087
pharmgkbrs10183087
gwascentralrs10183087
openSNPrs10183087
23andMers10183087
23andMe allrs10183087
SNP Nexus

SNPshotrs10183087
SNPdbers10183087
MSV3drs10183087
GWAS Ctlgrs10183087
GMAF0.2622
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 21526489] ICOS gene polymorphisms in B-cell chronic lymphocytic leukemia in the Polish population


[PMID 21917182OA-icon.png] ICOS gene polymorphisms are associated with sporadic breast cancer: a case-control study


[PMID 19202444] Association of genetic variation in inducible costimulator gene with outcome of kidney transplantation.


[PMID 19672595OA-icon.png] Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?


[PMID 19747393OA-icon.png] Improving power in genetic-association studies via wavelet transformation.


[PMID 22977635OA-icon.png] Association study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population


[PMID 24083358OA-icon.png] Effect of Soluble Inducible Costimulator Level and Its Polymorphisms on Age-Related Macular Degeneration


ClinVar
Risk rs10183087(C;C) rs10183087(G;G)
Alt rs10183087(C;C) rs10183087(G;G)
Reference Rs10183087(A;A)
Significance Probable-non-pathogenic
Disease Common Variable Immune Deficiency not specified
Variation info
Gene ICOS
CLNDBN Common Variable Immune Deficiency, Recessive not specified
Reversed 0
HGVS NC_000002.11:g.204824324A>C
CLNSRC
CLNACC RCV000311000.1, RCV000454953.1,