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rs9548988

From SNPedia

Orientationplus
Stabilizedplus
Make rs9548988(C;C)
Make rs9548988(C;T)
Make rs9548988(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position39931373
is asnp
is mentioned by
dbSNPrs9548988
ebirs9548988
HLIrs9548988
Exacrs9548988
Varsomers9548988
Maprs9548988
PheGenIrs9548988
hapmaprs9548988
1000 genomesrs9548988
hgdprs9548988
ensemblrs9548988
gopubmedrs9548988
geneviewrs9548988
scholarrs9548988
googlers9548988
pharmgkbrs9548988
gwascentralrs9548988
openSNPrs9548988
23andMers9548988
23andMe allrs9548988
SNP Nexus

SNPshotrs9548988
SNPdbers9548988
MSV3drs9548988
GWAS Ctlgrs9548988
GMAF0.4224
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19915572OA-icon.png]
Trait Ulcerative colitis
Title Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Risk Allele T
P-val 3E-7
Odds Ratio 1.10 [1.03-1.19]


GET Evidence
rs9548988
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary