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rs7664413

From SNPedia

Orientationplus
Stabilizedplus
Make rs7664413(C;C)
Make rs7664413(C;T)
Make rs7664413(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position176687553
GeneVEGFC
is asnp
is mentioned by
dbSNPrs7664413
ebirs7664413
HLIrs7664413
Exacrs7664413
Varsomers7664413
Maprs7664413
PheGenIrs7664413
hapmaprs7664413
1000 genomesrs7664413
hgdprs7664413
ensemblrs7664413
gopubmedrs7664413
geneviewrs7664413
scholarrs7664413
googlers7664413
pharmgkbrs7664413
gwascentralrs7664413
openSNPrs7664413
23andMers7664413
23andMe allrs7664413
SNP Nexus

SNPshotrs7664413
SNPdbers7664413
MSV3drs7664413
GWAS Ctlgrs7664413
GMAF0.2626
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20223440] Allelic variations in angiogenic pathway genes are associated with preeclampsia


[PMID 24478168] Role of VEGF-C Gene Polymorphisms in Susceptibility to Hepatocellular Carcinoma and Its Pathological Development