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rs4770877

From SNPedia

Orientationplus
Stabilizedplus
Make rs4770877(A;A)
Make rs4770877(A;G)
Make rs4770877(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position25761432
GeneATP8A2
is asnp
is mentioned by
dbSNPrs4770877
ebirs4770877
HLIrs4770877
Exacrs4770877
Varsomers4770877
Maprs4770877
PheGenIrs4770877
hapmaprs4770877
1000 genomesrs4770877
hgdprs4770877
ensemblrs4770877
gopubmedrs4770877
geneviewrs4770877
scholarrs4770877
googlers4770877
pharmgkbrs4770877
gwascentralrs4770877
openSNPrs4770877
23andMers4770877
23andMe allrs4770877
SNP Nexus

SNPshotrs4770877
SNPdbers4770877
MSV3drs4770877
GWAS Ctlgrs4770877
GMAF0.4853
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs4770877
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.531746
summary