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rs16905691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16905691(C;C)
Make rs16905691(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position54190139
GenePCDH15
is asnp
is mentioned by
dbSNPrs16905691
ebirs16905691
HLIrs16905691
Exacrs16905691
Varsomers16905691
Maprs16905691
PheGenIrs16905691
hapmaprs16905691
1000 genomesrs16905691
hgdprs16905691
ensemblrs16905691
gopubmedrs16905691
geneviewrs16905691
scholarrs16905691
googlers16905691
pharmgkbrs16905691
gwascentralrs16905691
openSNPrs16905691
23andMers16905691
23andMe allrs16905691
SNP Nexus

SNPshotrs16905691
SNPdbers16905691
MSV3drs16905691
GWAS Ctlgrs16905691
GMAF0.3691
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs16905691
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary