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rs4555132

From SNPedia

Orientationplus
Stabilizedplus
Make rs4555132(C;C)
Make rs4555132(C;T)
Make rs4555132(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position97396008
GeneRP11-461F11.1
is asnp
is mentioned by
dbSNPrs4555132
ebirs4555132
HLIrs4555132
Exacrs4555132
Varsomers4555132
Maprs4555132
PheGenIrs4555132
hapmaprs4555132
1000 genomesrs4555132
hgdprs4555132
ensemblrs4555132
gopubmedrs4555132
geneviewrs4555132
scholarrs4555132
googlers4555132
pharmgkbrs4555132
gwascentralrs4555132
openSNPrs4555132
23andMers4555132
23andMe allrs4555132
SNP Nexus

SNPshotrs4555132
SNPdbers4555132
MSV3drs4555132
GWAS Ctlgrs4555132
GMAF0.1979
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4555132
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.15625
summary