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rs4919910

From SNPedia

Orientationplus
Stabilizedplus
Make rs4919910(C;C)
Make rs4919910(C;T)
Make rs4919910(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome19
Position509717
GeneTPGS1
is asnp
is mentioned by
dbSNPrs4919910
ebirs4919910
HLIrs4919910
Exacrs4919910
Varsomers4919910
Maprs4919910
PheGenIrs4919910
hapmaprs4919910
1000 genomesrs4919910
hgdprs4919910
ensemblrs4919910
gopubmedrs4919910
geneviewrs4919910
scholarrs4919910
googlers4919910
pharmgkbrs4919910
gwascentralrs4919910
openSNPrs4919910
23andMers4919910
23andMe allrs4919910
SNP Nexus

SNPshotrs4919910
SNPdbers4919910
MSV3drs4919910
GWAS Ctlgrs4919910
GMAF0.4307
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4919910
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.578125
summary