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rs9472155

From SNPedia

Orientationplus
Stabilizedplus
Make rs9472155(C;C)
Make rs9472155(C;T)
Make rs9472155(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43929990
GeneLINC01512
is asnp
is mentioned by
dbSNPrs9472155
dbSNP (classic)rs9472155
ClinGenrs9472155
ebirs9472155
HLIrs9472155
Exacrs9472155
Gnomadrs9472155
Varsomers9472155
LitVarrs9472155
Maprs9472155
PheGenIrs9472155
Biobankrs9472155
1000 genomesrs9472155
hgdprs9472155
ensemblrs9472155
geneviewrs9472155
scholarrs9472155
googlers9472155
pharmgkbrs9472155
gwascentralrs9472155
openSNPrs9472155
23andMers9472155
SNPshotrs9472155
SNPdbers9472155
MSV3drs9472155
GWAS Ctlgrs9472155
GMAF0.2452
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21757650OA-icon.png]
Trait
Title Identification of cis- and trans-Acting Genetic Variants Explaining Up to Half the Variation in Circulating Vascular Endothelial Growth Factor Levels.
Risk Allele T
P-val 2E-26
Odds Ratio None None