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rs11110386

From SNPedia

Orientationplus
Stabilizedplus
Make rs11110386(C;C)
Make rs11110386(C;T)
Make rs11110386(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position100462559
is asnp
is mentioned by
dbSNPrs11110386
ebirs11110386
HLIrs11110386
Exacrs11110386
Varsomers11110386
Maprs11110386
PheGenIrs11110386
hapmaprs11110386
1000 genomesrs11110386
hgdprs11110386
ensemblrs11110386
gopubmedrs11110386
geneviewrs11110386
scholarrs11110386
googlers11110386
pharmgkbrs11110386
gwascentralrs11110386
openSNPrs11110386
23andMers11110386
23andMe allrs11110386
SNP Nexus

SNPshotrs11110386
SNPdbers11110386
MSV3drs11110386
GWAS Ctlgrs11110386
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25242139] Association of FXR gene variants with cholelithiasis