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rs9314986

From SNPedia

Orientationplus
Stabilizedplus
Make rs9314986(G;G)
Make rs9314986(G;T)
Make rs9314986(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position29884600
GeneLINC00297
is asnp
is mentioned by
dbSNPrs9314986
ebirs9314986
HLIrs9314986
Exacrs9314986
Varsomers9314986
Maprs9314986
PheGenIrs9314986
hapmaprs9314986
1000 genomesrs9314986
hgdprs9314986
ensemblrs9314986
gopubmedrs9314986
geneviewrs9314986
scholarrs9314986
googlers9314986
pharmgkbrs9314986
gwascentralrs9314986
openSNPrs9314986
23andMers9314986
23andMe allrs9314986
SNP Nexus

SNPshotrs9314986
SNPdbers9314986
MSV3drs9314986
GWAS Ctlgrs9314986
GMAF0.258
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20460270OA-icon.png]
Trait Biliary atresia
Title Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Risk Allele G
P-val 0.000002
Odds Ratio 2.95 [1.89-4.60]