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rs11653

From SNPedia

Orientationplus
Stabilizedplus
Make rs11653(A;A)
Make rs11653(A;T)
Make rs11653(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position128769526
GeneCALU
is asnp
is mentioned by
dbSNPrs11653
ebirs11653
HLIrs11653
Exacrs11653
Varsomers11653
Maprs11653
PheGenIrs11653
hapmaprs11653
1000 genomesrs11653
hgdprs11653
ensemblrs11653
gopubmedrs11653
geneviewrs11653
scholarrs11653
googlers11653
pharmgkbrs11653
gwascentralrs11653
openSNPrs11653
23andMers11653
23andMe allrs11653
SNP Nexus

SNPshotrs11653
SNPdbers11653
MSV3drs11653
GWAS Ctlgrs11653
GMAF0.2346
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 17048007OA-icon.png] Association of warfarin dose with genes involved in its action and metabolism.


GET Evidence
rs11653
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.25
summary