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rs16840493

From SNPedia

Orientationplus
Stabilizedplus
Make rs16840493(C;C)
Make rs16840493(C;T)
Make rs16840493(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position240704176
is asnp
is mentioned by
dbSNPrs16840493
ebirs16840493
HLIrs16840493
Exacrs16840493
Varsomers16840493
Maprs16840493
PheGenIrs16840493
hapmaprs16840493
1000 genomesrs16840493
hgdprs16840493
ensemblrs16840493
gopubmedrs16840493
geneviewrs16840493
scholarrs16840493
googlers16840493
pharmgkbrs16840493
gwascentralrs16840493
openSNPrs16840493
23andMers16840493
23andMe allrs16840493
SNP Nexus

SNPshotrs16840493
SNPdbers16840493
MSV3drs16840493
GWAS Ctlgrs16840493
GMAF0.1143
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16840493
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.132812
summary