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

rs7315438

From SNPedia

Orientationplus
Stabilizedplus
Make rs7315438(C;C)
Make rs7315438(C;T)
Make rs7315438(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position115453598
GeneLOC105370003
is asnp
is mentioned by
dbSNPrs7315438
dbSNP (classic)rs7315438
ClinGenrs7315438
ebirs7315438
HLIrs7315438
Exacrs7315438
Gnomadrs7315438
Varsomers7315438
LitVarrs7315438
Maprs7315438
PheGenIrs7315438
Biobankrs7315438
1000 genomesrs7315438
hgdprs7315438
ensemblrs7315438
geneviewrs7315438
scholarrs7315438
googlers7315438
pharmgkbrs7315438
gwascentralrs7315438
openSNPrs7315438
23andMers7315438
SNPshotrs7315438
SNPdbers7315438
MSV3drs7315438
GWAS Ctlgrs7315438
GMAF0.4555
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21761138OA-icon.png]
Trait
Title Meta-analysis of new genome-wide association studies of colorectal cancer risk.
Risk Allele
P-val 0.000006
Odds Ratio 1.1100 [1.06-1.15]


[PMID 32453900] Associations between lncRNA-related polymorphisms and hepatocellular carcinoma risk: A two-stage case-control study.