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rs34958067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34958067(C;T)
Make rs34958067(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position48413746
GenePLXNB1
is asnp
is mentioned by
dbSNPrs34958067
ebirs34958067
HLIrs34958067
Exacrs34958067
Varsomers34958067
Maprs34958067
PheGenIrs34958067
hapmaprs34958067
1000 genomesrs34958067
hgdprs34958067
ensemblrs34958067
gopubmedrs34958067
geneviewrs34958067
scholarrs34958067
googlers34958067
pharmgkbrs34958067
gwascentralrs34958067
openSNPrs34958067
23andMers34958067
23andMe allrs34958067
SNP Nexus

SNPshotrs34958067
SNPdbers34958067
MSV3drs34958067
GWAS Ctlgrs34958067
Max Magnitude0
Venter snp
Source plos
Gene PLXNB1
allele T
frequency
sift TOLERATED
HuRef 1103656089550
Disease Association Overexpressed and constitutively tyrosine phosphorylated in colon, liver, pancreas and gastric carcinoma cell lines. Overexpression increases MET activation and promotes invasive growth.