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rs4860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4860(C;C)
Make rs4860(C;T)
ReferenceGRCh37.p2 37.2/134
Chromosome12
Position63359783
GeneRPL14
is asnp
is mentioned by
dbSNPrs4860
ebirs4860
HLIrs4860
Exacrs4860
Varsomers4860
Maprs4860
PheGenIrs4860
hapmaprs4860
1000 genomesrs4860
hgdprs4860
ensemblrs4860
gopubmedrs4860
geneviewrs4860
scholarrs4860
googlers4860
pharmgkbrs4860
gwascentralrs4860
openSNPrs4860
23andMers4860
23andMe allrs4860
SNP Nexus

SNPshotrs4860
SNPdbers4860
MSV3drs4860
GWAS Ctlgrs4860
Max Magnitude0

[PMID 19551860] Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer [PMID 21080103] Catechol-O-methyltransferase (COMT) val158met polymorphism as a risk factor for PTSD after urban violence.

[PMID 26025199] Voxelwise eigenvector centrality mapping of the human functional connectome reveals an influence of the catechol-O-methyltransferase val158met polymorphism on the default mode and somatomotor network