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rs2296189

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2296189(A;G)
Make rs2296189(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position28319505
GeneFLT1
is asnp
is mentioned by
dbSNPrs2296189
ebirs2296189
HLIrs2296189
Exacrs2296189
Varsomers2296189
Maprs2296189
PheGenIrs2296189
hapmaprs2296189
1000 genomesrs2296189
hgdprs2296189
ensemblrs2296189
gopubmedrs2296189
geneviewrs2296189
scholarrs2296189
googlers2296189
pharmgkbrs2296189
gwascentralrs2296189
openSNPrs2296189
23andMers2296189
23andMe allrs2296189
SNP Nexus

SNPshotrs2296189
SNPdbers2296189
MSV3drs2296189
GWAS Ctlgrs2296189
GMAF0.1763
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 23794399] VEGFA, FLT1, KDR and colorectal cancer: Assessment of disease risk, tumor molecular phenotype, and survival


ClinVar
Risk rs2296189(G;G)
Alt rs2296189(G;G)
Reference rs2296189(A;A)
Significance Untested
Disease Carcinoma of colon
Variation info
Gene FLT1
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000013.10:g.28893642A>G
CLNSRC ClinVar
CLNACC RCV000149490.1,