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rs16844489

From SNPedia

Orientationplus
Stabilizedplus
Make rs16844489(C;C)
Make rs16844489(C;T)
Make rs16844489(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position137093276
is asnp
is mentioned by
dbSNPrs16844489
ebirs16844489
HLIrs16844489
Exacrs16844489
Varsomers16844489
Maprs16844489
PheGenIrs16844489
hapmaprs16844489
1000 genomesrs16844489
hgdprs16844489
ensemblrs16844489
gopubmedrs16844489
geneviewrs16844489
scholarrs16844489
googlers16844489
pharmgkbrs16844489
gwascentralrs16844489
openSNPrs16844489
23andMers16844489
23andMe allrs16844489
SNP Nexus

SNPshotrs16844489
SNPdbers16844489
MSV3drs16844489
GWAS Ctlgrs16844489
GMAF0.06198
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16844489
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0546875
summary