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rs1088967

From SNPedia

Merged intors204340
Orientationminus
Stabilizedminus
Make rs1088967(A;A)
Make rs1088967(A;G)
Make rs1088967(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position127010099
is asnp
is mentioned by
dbSNPrs1088967
ebirs1088967
HLIrs1088967
Exacrs1088967
Varsomers1088967
Maprs1088967
PheGenIrs1088967
hapmaprs1088967
1000 genomesrs1088967
hgdprs1088967
ensemblrs1088967
gopubmedrs1088967
geneviewrs1088967
scholarrs1088967
googlers1088967
pharmgkbrs1088967
gwascentralrs1088967
openSNPrs1088967
23andMers1088967
23andMe allrs1088967
SNP Nexus

SNPshotrs1088967
SNPdbers1088967
MSV3drs1088967
GWAS Ctlgrs1088967
StatusMerged into rs204340
Max Magnitude

[PMID 25680555] Interleukin-17FT7488 allele is associated with a decreased risk of colorectal cancer and tumor progression