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rs11179002

From SNPedia

Orientationplus
Stabilizedplus
Make rs11179002(C;C)
Make rs11179002(C;T)
Make rs11179002(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position71948504
GeneTPH2
is asnp
is mentioned by
dbSNPrs11179002
ebirs11179002
HLIrs11179002
Exacrs11179002
Varsomers11179002
Maprs11179002
PheGenIrs11179002
hapmaprs11179002
1000 genomesrs11179002
hgdprs11179002
ensemblrs11179002
gopubmedrs11179002
geneviewrs11179002
scholarrs11179002
googlers11179002
pharmgkbrs11179002
gwascentralrs11179002
openSNPrs11179002
23andMers11179002
23andMe allrs11179002
SNP Nexus

SNPshotrs11179002
SNPdbers11179002
MSV3drs11179002
GWAS Ctlgrs11179002
GMAF0.3205
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11179002
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.191667
summary