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

rs13213247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs13213247(A;C)
Make rs13213247(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position80806319
is asnp
is mentioned by
dbSNPrs13213247
ebirs13213247
HLIrs13213247
Exacrs13213247
Varsomers13213247
Maprs13213247
PheGenIrs13213247
hapmaprs13213247
1000 genomesrs13213247
hgdprs13213247
ensemblrs13213247
gopubmedrs13213247
geneviewrs13213247
scholarrs13213247
googlers13213247
pharmgkbrs13213247
gwascentralrs13213247
openSNPrs13213247
23andMers13213247
23andMe allrs13213247
SNP Nexus

SNPshotrs13213247
SNPdbers13213247
MSV3drs13213247
GWAS Ctlgrs13213247
GMAF0.09229
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 19756043OA-icon.png] A simple and efficient algorithm for genome-wide homozygosity analysis in disease.


GET Evidence
rs13213247
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0409836
summary