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rs2120991

From SNPedia

Orientationplus
Stabilizedplus
Make rs2120991(A;A)
Make rs2120991(A;C)
Make rs2120991(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position53876444
is asnp
is mentioned by
dbSNPrs2120991
ebirs2120991
HLIrs2120991
Exacrs2120991
Varsomers2120991
Maprs2120991
PheGenIrs2120991
hapmaprs2120991
1000 genomesrs2120991
hgdprs2120991
ensemblrs2120991
gopubmedrs2120991
geneviewrs2120991
scholarrs2120991
googlers2120991
pharmgkbrs2120991
gwascentralrs2120991
openSNPrs2120991
23andMers2120991
23andMe allrs2120991
SNP Nexus

SNPshotrs2120991
SNPdbers2120991
MSV3drs2120991
GWAS Ctlgrs2120991
GMAF0.2264
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 0.000009
Odds Ratio 2.14 [1.58-2.89]