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

rs10495669

From SNPedia

Orientationplus
Stabilizedplus
Make rs10495669(C;C)
Make rs10495669(C;G)
Make rs10495669(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position17844006
is asnp
is mentioned by
dbSNPrs10495669
ebirs10495669
HLIrs10495669
Exacrs10495669
Varsomers10495669
Maprs10495669
PheGenIrs10495669
hapmaprs10495669
1000 genomesrs10495669
hgdprs10495669
ensemblrs10495669
gopubmedrs10495669
geneviewrs10495669
scholarrs10495669
googlers10495669
pharmgkbrs10495669
gwascentralrs10495669
openSNPrs10495669
23andMers10495669
23andMe allrs10495669
SNP Nexus

SNPshotrs10495669
SNPdbers10495669
MSV3drs10495669
GWAS Ctlgrs10495669
GMAF0.3958
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 17903299OA-icon.png] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.


GET Evidence
rs10495669
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.492188
summary