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rs16841722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16841722(C;C)
Make rs16841722(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position157421701
GeneCYTIP
is asnp
is mentioned by
dbSNPrs16841722
ebirs16841722
HLIrs16841722
Exacrs16841722
Varsomers16841722
Maprs16841722
PheGenIrs16841722
hapmaprs16841722
1000 genomesrs16841722
hgdprs16841722
ensemblrs16841722
gopubmedrs16841722
geneviewrs16841722
scholarrs16841722
googlers16841722
pharmgkbrs16841722
gwascentralrs16841722
openSNPrs16841722
23andMers16841722
23andMe allrs16841722
SNP Nexus

SNPshotrs16841722
SNPdbers16841722
MSV3drs16841722
GWAS Ctlgrs16841722
GMAF0.04959
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16841722
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0546875
summary