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rs13156607

From SNPedia

Orientationplus
Stabilizedplus
Make rs13156607(C;C)
Make rs13156607(C;T)
Make rs13156607(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position169472983
is asnp
is mentioned by
dbSNPrs13156607
ebirs13156607
HLIrs13156607
Exacrs13156607
Varsomers13156607
Maprs13156607
PheGenIrs13156607
hapmaprs13156607
1000 genomesrs13156607
hgdprs13156607
ensemblrs13156607
gopubmedrs13156607
geneviewrs13156607
scholarrs13156607
googlers13156607
pharmgkbrs13156607
gwascentralrs13156607
openSNPrs13156607
23andMers13156607
23andMe allrs13156607
SNP Nexus

SNPshotrs13156607
SNPdbers13156607
MSV3drs13156607
GWAS Ctlgrs13156607
GMAF0.2617
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20966902OA-icon.png]
Trait
Title Genome-Wide Association Study of Anthropometric Traits and Evidence of Interactions With Age and Study Year in Filipino Women
Risk Allele T
P-val 0.000005
Odds Ratio 3.9100 [2.24-5.58] cm increase