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rs4919908

From SNPedia

Orientationplus
Stabilizedplus
Make rs4919908(C;C)
Make rs4919908(C;T)
Make rs4919908(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome19
Position508626
GeneTPGS1
is asnp
is mentioned by
dbSNPrs4919908
ebirs4919908
HLIrs4919908
Exacrs4919908
Varsomers4919908
Maprs4919908
PheGenIrs4919908
hapmaprs4919908
1000 genomesrs4919908
hgdprs4919908
ensemblrs4919908
gopubmedrs4919908
geneviewrs4919908
scholarrs4919908
googlers4919908
pharmgkbrs4919908
gwascentralrs4919908
openSNPrs4919908
23andMers4919908
23andMe allrs4919908
SNP Nexus

SNPshotrs4919908
SNPdbers4919908
MSV3drs4919908
GWAS Ctlgrs4919908
GMAF0.4284
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4919908
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.5625
summary