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rs1861525

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1861525(A;G)
Make rs1861525(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position25121983
GeneCYCS
is asnp
is mentioned by
dbSNPrs1861525
dbSNP (classic)rs1861525
ClinGenrs1861525
ebirs1861525
HLIrs1861525
Exacrs1861525
Gnomadrs1861525
Varsomers1861525
LitVarrs1861525
Maprs1861525
PheGenIrs1861525
Biobankrs1861525
1000 genomesrs1861525
hgdprs1861525
ensemblrs1861525
geneviewrs1861525
scholarrs1861525
googlers1861525
pharmgkbrs1861525
gwascentralrs1861525
openSNPrs1861525
23andMers1861525
SNPshotrs1861525
SNPdbers1861525
MSV3drs1861525
GWAS Ctlgrs1861525
GMAF0.02112
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 2E-7
Odds Ratio .25 unit decrease


[PMID 19838195OA-icon.png] A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.


ClinVar
Risk rs1861525(G;G)
Alt rs1861525(G;G)
Reference Rs1861525(A;A)
Significance Probable-non-pathogenic
Disease Thrombocytopenia
Variation info
Gene CYCS
CLNDBN Thrombocytopenia
Reversed 0
HGVS NC_000007.13:g.25161602A>G
CLNSRC
CLNACC RCV000306671.1,