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

rs387907326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907326(G;T)
Make rs387907326(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position33279841
GeneIL10RB
is asnp
is mentioned by
dbSNPrs387907326
ebirs387907326
HLIrs387907326
Exacrs387907326
Varsomers387907326
Maprs387907326
PheGenIrs387907326
hapmaprs387907326
1000 genomesrs387907326
hgdprs387907326
ensemblrs387907326
gopubmedrs387907326
geneviewrs387907326
scholarrs387907326
googlers387907326
pharmgkbrs387907326
gwascentralrs387907326
openSNPrs387907326
23andMers387907326
23andMe allrs387907326
SNP Nexus

SNPshotrs387907326
SNPdbers387907326
MSV3drs387907326
GWAS Ctlgrs387907326
Max Magnitude0
ClinVar
Risk rs387907326(A,T;A,T)
Alt rs387907326(A,T;A,T)
Reference rs387907326(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.34652146G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034826.28,