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rs139606545

From SNPedia

Merged intors13397172
Orientationplus
Make rs139606545(C;C)
Make rs139606545(C;T)
Make rs139606545(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position199180316
is asnp
is mentioned by
dbSNPrs139606545
ebirs139606545
HLIrs139606545
Exacrs139606545
Varsomers139606545
Maprs139606545
PheGenIrs139606545
hapmaprs139606545
1000 genomesrs139606545
hgdprs139606545
ensemblrs139606545
gopubmedrs139606545
geneviewrs139606545
scholarrs139606545
googlers139606545
pharmgkbrs139606545
gwascentralrs139606545
openSNPrs139606545
23andMers139606545
23andMe allrs139606545
SNP Nexus

SNPshotrs139606545
SNPdbers139606545
MSV3drs139606545
GWAS Ctlgrs139606545
StatusMerged into rs13397172
Max Magnitude

[PMID 27527254] Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.