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rs11694911

From SNPedia

Orientationplus
Stabilizedplus
Make rs11694911(C;C)
Make rs11694911(C;T)
Make rs11694911(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position10433072
is asnp
is mentioned by
dbSNPrs11694911
dbSNP (old)rs11694911
ClinGenrs11694911
ebirs11694911
HLIrs11694911
Exacrs11694911
Gnomadrs11694911
Varsomers11694911
LitVarrs11694911
Maprs11694911
PheGenIrs11694911
Biobankrs11694911
1000 genomesrs11694911
hgdprs11694911
ensemblrs11694911
gopubmedrs11694911
geneviewrs11694911
scholarrs11694911
googlers11694911
pharmgkbrs11694911
gwascentralrs11694911
openSNPrs11694911
23andMers11694911
23andMe allrs11694911
SNPshotrs11694911
SNPdbers11694911
MSV3drs11694911
GWAS Ctlgrs11694911
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 29425227OA-icon.png] Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations.