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rs10108511

From SNPedia

Orientationplus
Make rs10108511(C;C)
Make rs10108511(C;T)
Make rs10108511(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position11578007
GeneLINC00208
is asnp
is mentioned by
dbSNPrs10108511
ebirs10108511
HLIrs10108511
Exacrs10108511
Varsomers10108511
Maprs10108511
PheGenIrs10108511
hapmaprs10108511
1000 genomesrs10108511
hgdprs10108511
ensemblrs10108511
gopubmedrs10108511
geneviewrs10108511
scholarrs10108511
googlers10108511
pharmgkbrs10108511
gwascentralrs10108511
openSNPrs10108511
23andMers10108511
23andMe allrs10108511
SNP Nexus

SNPshotrs10108511
SNPdbers10108511
MSV3drs10108511
GWAS Ctlgrs10108511
Max Magnitude
? (C;C) (C;T) (T;T) 28

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