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rs11571364

From SNPedia

Orientationplus
Stabilizedplus
Make rs11571364(A;A)
Make rs11571364(A;G)
Make rs11571364(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7008372
GeneALOX12, LOC100506713
is asnp
is mentioned by
dbSNPrs11571364
ebirs11571364
HLIrs11571364
Exacrs11571364
Varsomers11571364
Maprs11571364
PheGenIrs11571364
hapmaprs11571364
1000 genomesrs11571364
hgdprs11571364
ensemblrs11571364
gopubmedrs11571364
geneviewrs11571364
scholarrs11571364
googlers11571364
pharmgkbrs11571364
gwascentralrs11571364
openSNPrs11571364
23andMers11571364
23andMe allrs11571364
SNP Nexus

SNPshotrs11571364
SNPdbers11571364
MSV3drs11571364
GWAS Ctlgrs11571364
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24908683OA-icon.png] Genetic variation in prostaglandin synthesis and related pathways, NSAID use, and colorectal cancer risk in the Colon Cancer Family Registry