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rs16944011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16944011(C;G)
Make rs16944011(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position27712399
is asnp
is mentioned by
dbSNPrs16944011
ebirs16944011
HLIrs16944011
Exacrs16944011
Varsomers16944011
Maprs16944011
PheGenIrs16944011
hapmaprs16944011
1000 genomesrs16944011
hgdprs16944011
ensemblrs16944011
gopubmedrs16944011
geneviewrs16944011
scholarrs16944011
googlers16944011
pharmgkbrs16944011
gwascentralrs16944011
openSNPrs16944011
23andMers16944011
23andMe allrs16944011
SNP Nexus

SNPshotrs16944011
SNPdbers16944011
MSV3drs16944011
GWAS Ctlgrs16944011
GMAF0.06566
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs16944011
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.101562
summary