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rs1358980

From SNPedia

Orientationplus
Stabilizedplus
Make rs1358980(C;C)
Make rs1358980(C;T)
Make rs1358980(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43796814
is asnp
is mentioned by
dbSNPrs1358980
ebirs1358980
HLIrs1358980
Exacrs1358980
Varsomers1358980
Maprs1358980
PheGenIrs1358980
hapmaprs1358980
1000 genomesrs1358980
hgdprs1358980
ensemblrs1358980
gopubmedrs1358980
geneviewrs1358980
scholarrs1358980
googlers1358980
pharmgkbrs1358980
gwascentralrs1358980
openSNPrs1358980
23andMers1358980
23andMe allrs1358980
SNP Nexus

SNPshotrs1358980
SNPdbers1358980
MSV3drs1358980
GWAS Ctlgrs1358980
GMAF0.4389
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23754948OA-icon.png]
Trait Sexual dimorphism in anthropometric traits
Title Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
Risk Allele T
P-val 2E-11
Odds Ratio NR NR


[PMID 19308252OA-icon.png] Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.