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rs137853579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853579(A;A)
Make rs137853579(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117993294
GeneIL10RA
is asnp
is mentioned by
dbSNPrs137853579
ebirs137853579
HLIrs137853579
Exacrs137853579
Varsomers137853579
Maprs137853579
PheGenIrs137853579
hapmaprs137853579
1000 genomesrs137853579
hgdprs137853579
ensemblrs137853579
gopubmedrs137853579
geneviewrs137853579
scholarrs137853579
googlers137853579
pharmgkbrs137853579
gwascentralrs137853579
openSNPrs137853579
23andMers137853579
23andMe allrs137853579
SNP Nexus

SNPshotrs137853579
SNPdbers137853579
MSV3drs137853579
GWAS Ctlgrs137853579
Max Magnitude0
OMIM146933
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853579(A;A)
Alt rs137853579(A;A)
Reference rs137853579(G;G)
Significance Pathogenic
Disease Inflammatory bowel disease 28
Variation info
Gene IL10RA
CLNDBN Inflammatory bowel disease 28
Reversed 0
HGVS NC_000011.9:g.117864009G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015937.25,