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rs17172185

From SNPedia

Orientationplus
Stabilizedplus
Make rs17172185(C;C)
Make rs17172185(C;T)
Make rs17172185(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position43247240
GeneHECW1, LOC102724911
is asnp
is mentioned by
dbSNPrs17172185
ebirs17172185
HLIrs17172185
Exacrs17172185
Varsomers17172185
Maprs17172185
PheGenIrs17172185
hapmaprs17172185
1000 genomesrs17172185
hgdprs17172185
ensemblrs17172185
gopubmedrs17172185
geneviewrs17172185
scholarrs17172185
googlers17172185
pharmgkbrs17172185
gwascentralrs17172185
openSNPrs17172185
23andMers17172185
23andMe allrs17172185
SNP Nexus

SNPshotrs17172185
SNPdbers17172185
MSV3drs17172185
GWAS Ctlgrs17172185
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24121790OA-icon.png]
Trait Esophageal adenocarcinoma
Title A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
Risk Allele T
P-val 5E-6
Odds Ratio 1.47 [1.25-1.75]