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rs1679013

From SNPedia

Orientationplus
Stabilizedplus
Make rs1679013(C;C)
Make rs1679013(C;T)
Make rs1679013(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22206988
is asnp
is mentioned by
dbSNPrs1679013
ebirs1679013
HLIrs1679013
Exacrs1679013
Varsomers1679013
Maprs1679013
PheGenIrs1679013
hapmaprs1679013
1000 genomesrs1679013
hgdprs1679013
ensemblrs1679013
gopubmedrs1679013
geneviewrs1679013
scholarrs1679013
googlers1679013
pharmgkbrs1679013
gwascentralrs1679013
openSNPrs1679013
23andMers1679013
23andMe allrs1679013
SNP Nexus

SNPshotrs1679013
SNPdbers1679013
MSV3drs1679013
GWAS Ctlgrs1679013
GMAF0.4871
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele C
P-val 1E-8
Odds Ratio 1.19 [1.12-1.27]