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rs1035209

From SNPedia

Orientationplus
Stabilizedplus
Make rs1035209(C;C)
Make rs1035209(C;T)
Make rs1035209(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position99585609
is asnp
is mentioned by
dbSNPrs1035209
dbSNP (classic)rs1035209
ClinGenrs1035209
ebirs1035209
HLIrs1035209
Exacrs1035209
Gnomadrs1035209
Varsomers1035209
LitVarrs1035209
Maprs1035209
PheGenIrs1035209
Biobankrs1035209
1000 genomesrs1035209
hgdprs1035209
ensemblrs1035209
geneviewrs1035209
scholarrs1035209
googlers1035209
pharmgkbrs1035209
gwascentralrs1035209
openSNPrs1035209
23andMers1035209
SNPshotrs1035209
SNPdbers1035209
MSV3drs1035209
GWAS Ctlgrs1035209
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 24737748OA-icon.png]
Trait Colorectal cancer
Title Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Risk Allele T
P-val 5E-11
Odds Ratio 1.12 [1.08-1.16]