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rs10500264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10500264(A;A)
Make rs10500264(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position33259408
is asnp
is mentioned by
dbSNPrs10500264
ebirs10500264
HLIrs10500264
Exacrs10500264
Varsomers10500264
Maprs10500264
PheGenIrs10500264
hapmaprs10500264
1000 genomesrs10500264
hgdprs10500264
ensemblrs10500264
gopubmedrs10500264
geneviewrs10500264
scholarrs10500264
googlers10500264
pharmgkbrs10500264
gwascentralrs10500264
openSNPrs10500264
23andMers10500264
23andMe allrs10500264
SNP Nexus

SNPshotrs10500264
SNPdbers10500264
MSV3drs10500264
GWAS Ctlgrs10500264
GMAF0.1189
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19915574OA-icon.png]
Trait Inflammatory bowel disease (early onset)
Title Common variants at five new loci associated with early-onset inflammatory bowel disease
Risk Allele
P-val 4E-10
Odds Ratio 1.21 [1.11-1.31]


GET Evidence
rs10500264
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary