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rs137853580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853580(C;T)
Make rs137853580(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117989504
GeneIL10RA
is asnp
is mentioned by
dbSNPrs137853580
ebirs137853580
HLIrs137853580
Exacrs137853580
Varsomers137853580
Maprs137853580
PheGenIrs137853580
hapmaprs137853580
1000 genomesrs137853580
hgdprs137853580
ensemblrs137853580
gopubmedrs137853580
geneviewrs137853580
scholarrs137853580
googlers137853580
pharmgkbrs137853580
gwascentralrs137853580
openSNPrs137853580
23andMers137853580
23andMe allrs137853580
SNP Nexus

SNPshotrs137853580
SNPdbers137853580
MSV3drs137853580
GWAS Ctlgrs137853580
Max Magnitude0
OMIM146933
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853580(T;T)
Alt rs137853580(T;T)
Reference rs137853580(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.117860219C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015938.27,