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rs16988013

From SNPedia

Orientationplus
Stabilizedplus
Make rs16988013(C;C)
Make rs16988013(C;T)
Make rs16988013(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position27838276
is asnp
is mentioned by
dbSNPrs16988013
ebirs16988013
HLIrs16988013
Exacrs16988013
Varsomers16988013
Maprs16988013
PheGenIrs16988013
hapmaprs16988013
1000 genomesrs16988013
hgdprs16988013
ensemblrs16988013
gopubmedrs16988013
geneviewrs16988013
scholarrs16988013
googlers16988013
pharmgkbrs16988013
gwascentralrs16988013
openSNPrs16988013
23andMers16988013
23andMe allrs16988013
SNP Nexus

SNPshotrs16988013
SNPdbers16988013
MSV3drs16988013
GWAS Ctlgrs16988013
GMAF0.03265
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16988013
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0434783
summary