Have questions? Visit https://www.reddit.com/r/SNPedia

rs4730276

From SNPedia

Orientationplus
Stabilizedplus
Make rs4730276(A;A)
Make rs4730276(A;G)
Make rs4730276(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107843992
is asnp
is mentioned by
dbSNPrs4730276
ebirs4730276
HLIrs4730276
Exacrs4730276
Varsomers4730276
Maprs4730276
PheGenIrs4730276
hapmaprs4730276
1000 genomesrs4730276
hgdprs4730276
ensemblrs4730276
gopubmedrs4730276
geneviewrs4730276
scholarrs4730276
googlers4730276
pharmgkbrs4730276
gwascentralrs4730276
openSNPrs4730276
23andMers4730276
23andMe allrs4730276
SNP Nexus

SNPshotrs4730276
SNPdbers4730276
MSV3drs4730276
GWAS Ctlgrs4730276
GMAF0.3333
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19122664OA-icon.png]
Trait Ulcerative colitis
Title Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
Risk Allele
P-val 0.000009
Odds Ratio 1.22 None



GET Evidence
rs4730276
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.325397
summary