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rs886774

From SNPedia

Orientationplus
Stabilizedplus
Make rs886774(A;A)
Make rs886774(A;G)
Make rs886774(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107854989
is asnp
is mentioned by
dbSNPrs886774
ebirs886774
HLIrs886774
Exacrs886774
Varsomers886774
Maprs886774
PheGenIrs886774
hapmaprs886774
1000 genomesrs886774
hgdprs886774
ensemblrs886774
gopubmedrs886774
geneviewrs886774
scholarrs886774
googlers886774
pharmgkbrs886774
gwascentralrs886774
openSNPrs886774
23andMers886774
23andMe allrs886774
SNP Nexus

SNPshotrs886774
SNPdbers886774
MSV3drs886774
GWAS Ctlgrs886774
GMAF0.2975
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 3E-8
Odds Ratio 1.11 [1.03-1.19]


GET Evidence
rs886774
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary