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rs4774925

From SNPedia

Orientationplus
Stabilizedplus
Make rs4774925(C;C)
Make rs4774925(C;T)
Make rs4774925(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position57312204
is asnp
is mentioned by
dbSNPrs4774925
ebirs4774925
HLIrs4774925
Exacrs4774925
Varsomers4774925
Maprs4774925
PheGenIrs4774925
hapmaprs4774925
1000 genomesrs4774925
hgdprs4774925
ensemblrs4774925
gopubmedrs4774925
geneviewrs4774925
scholarrs4774925
googlers4774925
pharmgkbrs4774925
gwascentralrs4774925
openSNPrs4774925
23andMers4774925
23andMe allrs4774925
SNP Nexus

SNPshotrs4774925
SNPdbers4774925
MSV3drs4774925
GWAS Ctlgrs4774925
GMAF0.4646
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4774925
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.492188
summary