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rs6823379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6823379(C;C)
Make rs6823379(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position41709845
is asnp
is mentioned by
dbSNPrs6823379
ebirs6823379
HLIrs6823379
Exacrs6823379
Varsomers6823379
Maprs6823379
PheGenIrs6823379
hapmaprs6823379
1000 genomesrs6823379
hgdprs6823379
ensemblrs6823379
gopubmedrs6823379
geneviewrs6823379
scholarrs6823379
googlers6823379
pharmgkbrs6823379
gwascentralrs6823379
openSNPrs6823379
23andMers6823379
23andMe allrs6823379
SNP Nexus

SNPshotrs6823379
SNPdbers6823379
MSV3drs6823379
GWAS Ctlgrs6823379
GMAF0.1524
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 17903293OA-icon.png] Genome-wide association with select biomarker traits in the Framingham Heart Study.


GET Evidence
rs6823379
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.234375
summary