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rs10781500

From SNPedia

Orientationplus
Stabilizedplus
Make rs10781500(C;C)
Make rs10781500(C;T)
Make rs10781500(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136374886
GeneCARD9
is asnp
is mentioned by
dbSNPrs10781500
ebirs10781500
HLIrs10781500
Exacrs10781500
Varsomers10781500
Maprs10781500
PheGenIrs10781500
hapmaprs10781500
1000 genomesrs10781500
hgdprs10781500
ensemblrs10781500
gopubmedrs10781500
geneviewrs10781500
scholarrs10781500
googlers10781500
pharmgkbrs10781500
gwascentralrs10781500
openSNPrs10781500
23andMers10781500
23andMe allrs10781500
SNP Nexus

SNPshotrs10781500
SNPdbers10781500
MSV3drs10781500
GWAS Ctlgrs10781500
GMAF0.3655
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
P-val 0.000007
Odds Ratio NR NR
GWAS snp
PMID [PMID 21743469OA-icon.png]
Trait
Title Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
Risk Allele T
P-val 0.000001
Odds Ratio None None


GET Evidence
rs10781500
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.304688
summary