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rs4650977

From SNPedia

Orientationplus
Stabilizedplus
Make rs4650977(C;C)
Make rs4650977(C;G)
Make rs4650977(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position177808473
is asnp
is mentioned by
dbSNPrs4650977
ebirs4650977
HLIrs4650977
Exacrs4650977
Varsomers4650977
Maprs4650977
PheGenIrs4650977
hapmaprs4650977
1000 genomesrs4650977
hgdprs4650977
ensemblrs4650977
gopubmedrs4650977
geneviewrs4650977
scholarrs4650977
googlers4650977
pharmgkbrs4650977
gwascentralrs4650977
openSNPrs4650977
23andMers4650977
23andMe allrs4650977
SNP Nexus

SNPshotrs4650977
SNPdbers4650977
MSV3drs4650977
GWAS Ctlgrs4650977
GMAF0.4376
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs4650977
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.476562
summary