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rs4730273

From SNPedia

Orientationplus
Stabilizedplus
Make rs4730273(A;A)
Make rs4730273(A;C)
Make rs4730273(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position107839074
is asnp
is mentioned by
dbSNPrs4730273
ebirs4730273
HLIrs4730273
Exacrs4730273
Varsomers4730273
Maprs4730273
PheGenIrs4730273
hapmaprs4730273
1000 genomesrs4730273
hgdprs4730273
ensemblrs4730273
gopubmedrs4730273
geneviewrs4730273
scholarrs4730273
googlers4730273
pharmgkbrs4730273
gwascentralrs4730273
openSNPrs4730273
23andMers4730273
23andMe allrs4730273
SNP Nexus

SNPshotrs4730273
SNPdbers4730273
MSV3drs4730273
GWAS Ctlgrs4730273
GMAF0.2948
Max Magnitude
? (A;A) (A;C) (C;C) 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 0.000005
Odds Ratio 1.22 None



GET Evidence
rs4730273
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary