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rs16860281

From SNPedia

Orientationplus
Stabilizedplus
Make rs16860281(C;C)
Make rs16860281(C;T)
Make rs16860281(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148277560
is asnp
is mentioned by
dbSNPrs16860281
ebirs16860281
HLIrs16860281
Exacrs16860281
Varsomers16860281
Maprs16860281
PheGenIrs16860281
hapmaprs16860281
1000 genomesrs16860281
hgdprs16860281
ensemblrs16860281
gopubmedrs16860281
geneviewrs16860281
scholarrs16860281
googlers16860281
pharmgkbrs16860281
gwascentralrs16860281
openSNPrs16860281
23andMers16860281
23andMe allrs16860281
SNP Nexus

SNPshotrs16860281
SNPdbers16860281
MSV3drs16860281
GWAS Ctlgrs16860281
GMAF0.08678
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16860281
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.109375
summary