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rs929156

From SNPedia

Orientationminus
Stabilizedminus
Make rs929156(C;C)
Make rs929156(C;T)
Make rs929156(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30171922
GeneTRIM15
is asnp
is mentioned by
dbSNPrs929156
ebirs929156
HLIrs929156
Exacrs929156
Varsomers929156
Maprs929156
PheGenIrs929156
hapmaprs929156
1000 genomesrs929156
hgdprs929156
ensemblrs929156
gopubmedrs929156
geneviewrs929156
scholarrs929156
googlers929156
pharmgkbrs929156
gwascentralrs929156
openSNPrs929156
23andMers929156
23andMe allrs929156
SNP Nexus

SNPshotrs929156
SNPdbers929156
MSV3drs929156
GWAS Ctlgrs929156
GMAF0.2006
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19010793OA-icon.png] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.


GET Evidence
TRIM15-S324N
aa_change Ser324Asn
aa_change_short S324N
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.181273
summary