Have questions? Visit https://www.reddit.com/r/SNPedia

rs10486275

From SNPedia

Orientationplus
Stabilizedplus
Make rs10486275(C;C)
Make rs10486275(C;T)
Make rs10486275(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position8963946
is asnp
is mentioned by
dbSNPrs10486275
ebirs10486275
HLIrs10486275
Exacrs10486275
Varsomers10486275
Maprs10486275
PheGenIrs10486275
hapmaprs10486275
1000 genomesrs10486275
hgdprs10486275
ensemblrs10486275
gopubmedrs10486275
geneviewrs10486275
scholarrs10486275
googlers10486275
pharmgkbrs10486275
gwascentralrs10486275
openSNPrs10486275
23andMers10486275
23andMe allrs10486275
SNP Nexus

SNPshotrs10486275
SNPdbers10486275
MSV3drs10486275
GWAS Ctlgrs10486275
GMAF0.2309
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs10486275
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.257812
summary