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

rs368287711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368287711(A;A)
Make rs368287711(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position117989554
GeneIL10RA
is asnp
is mentioned by
dbSNPrs368287711
ebirs368287711
HLIrs368287711
Exacrs368287711
Varsomers368287711
Maprs368287711
PheGenIrs368287711
hapmaprs368287711
1000 genomesrs368287711
hgdprs368287711
ensemblrs368287711
gopubmedrs368287711
geneviewrs368287711
scholarrs368287711
googlers368287711
pharmgkbrs368287711
gwascentralrs368287711
openSNPrs368287711
23andMers368287711
23andMe allrs368287711
SNP Nexus

SNPshotrs368287711
SNPdbers368287711
MSV3drs368287711
GWAS Ctlgrs368287711
Max Magnitude0
ClinVar
Risk rs368287711(A,T;A,T)
Alt rs368287711(A,T;A,T)
Reference rs368287711(C;C)
Significance Pathogenic
Disease Inflammatory bowel disease 28
Variation info
Gene IL10RA
CLNDBN Inflammatory bowel disease 28
Reversed 0
HGVS NC_000011.9:g.117860269C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032627.26,