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rs587776843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776843(C;C)
Make rs587776843(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position206775286
is asnp
is mentioned by
dbSNPrs587776843
ebirs587776843
HLIrs587776843
Exacrs587776843
Varsomers587776843
Maprs587776843
PheGenIrs587776843
hapmaprs587776843
1000 genomesrs587776843
hgdprs587776843
ensemblrs587776843
gopubmedrs587776843
geneviewrs587776843
scholarrs587776843
googlers587776843
pharmgkbrs587776843
gwascentralrs587776843
openSNPrs587776843
23andMers587776843
23andMe allrs587776843
SNP Nexus

SNPshotrs587776843
SNPdbers587776843
MSV3drs587776843
GWAS Ctlgrs587776843
Max Magnitude0
ClinVar
Risk rs587776843(C,T;C,T)
Alt rs587776843(C,T;C,T)
Reference rs587776843(A;A)
Significance Pathogenic
Disease Rheumatoid arthritis
Variation info
Gene IL10
CLNDBN Rheumatoid arthritis, progression of
Reversed 1
HGVS NC_000001.10:g.206948631T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018370.29,