Have questions? Visit https://www.reddit.com/r/SNPedia

rs10932037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs10932037(C;T)
Make rs10932037(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203960623
GeneICOS
is asnp
is mentioned by
dbSNPrs10932037
dbSNP (old)rs10932037
ClinGenrs10932037
ebirs10932037
HLIrs10932037
Exacrs10932037
Gnomadrs10932037
Varsomers10932037
Maprs10932037
PheGenIrs10932037
Biobankrs10932037
1000 genomesrs10932037
hgdprs10932037
ensemblrs10932037
gopubmedrs10932037
geneviewrs10932037
scholarrs10932037
googlers10932037
pharmgkbrs10932037
gwascentralrs10932037
openSNPrs10932037
23andMers10932037
23andMe allrs10932037
SNP Nexus

SNPshotrs10932037
SNPdbers10932037
MSV3drs10932037
GWAS Ctlgrs10932037
GMAF0.07025
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19175525OA-icon.png] CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data


[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 18200060] PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not.


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


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


ClinVar
Risk rs10932037(T;T)
Alt rs10932037(T;T)
Reference Rs10932037(C;C)
Significance Probable-non-pathogenic
Disease Common Variable Immune Deficiency
Variation info
Gene ICOS
CLNDBN Common Variable Immune Deficiency, Recessive
Reversed 0
HGVS NC_000002.11:g.204825346C>T
CLNSRC
CLNACC RCV000325562.1,