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rs149491038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149491038(C;T)
Make rs149491038(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117995684
GeneIL10RA
is asnp
is mentioned by
dbSNPrs149491038
ebirs149491038
HLIrs149491038
Exacrs149491038
Varsomers149491038
Maprs149491038
PheGenIrs149491038
hapmaprs149491038
1000 genomesrs149491038
hgdprs149491038
ensemblrs149491038
gopubmedrs149491038
geneviewrs149491038
scholarrs149491038
googlers149491038
pharmgkbrs149491038
gwascentralrs149491038
openSNPrs149491038
23andMers149491038
23andMe allrs149491038
SNP Nexus

SNPshotrs149491038
SNPdbers149491038
MSV3drs149491038
GWAS Ctlgrs149491038
Max Magnitude0
ClinVar
Risk rs149491038(T;T)
Alt rs149491038(T;T)
Reference rs149491038(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.117866399C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032625.25,