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rs121909601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909601(A;A)
Make rs121909601(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position33279897
GeneIL10RB
is asnp
is mentioned by
dbSNPrs121909601
ebirs121909601
HLIrs121909601
Exacrs121909601
Varsomers121909601
Maprs121909601
PheGenIrs121909601
hapmaprs121909601
1000 genomesrs121909601
hgdprs121909601
ensemblrs121909601
gopubmedrs121909601
geneviewrs121909601
scholarrs121909601
googlers121909601
pharmgkbrs121909601
gwascentralrs121909601
openSNPrs121909601
23andMers121909601
23andMe allrs121909601
SNP Nexus

SNPshotrs121909601
SNPdbers121909601
MSV3drs121909601
GWAS Ctlgrs121909601
Max Magnitude0
OMIM123889
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909601(A;A)
Alt rs121909601(A;A)
Reference rs121909601(G;G)
Significance Pathogenic
Disease Inflammatory bowel disease 25
Variation info
Gene IL10RB
CLNDBN Inflammatory bowel disease 25, autosomal recessive
Reversed 0
HGVS NC_000021.8:g.34652202G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018432.27,