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rs869312889

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312889(C;T)
Make rs869312889(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42322395
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312889
ebirs869312889
HLIrs869312889
Exacrs869312889
Varsomers869312889
Maprs869312889
PheGenIrs869312889
hapmaprs869312889
1000 genomesrs869312889
hgdprs869312889
ensemblrs869312889
gopubmedrs869312889
geneviewrs869312889
scholarrs869312889
googlers869312889
pharmgkbrs869312889
gwascentralrs869312889
openSNPrs869312889
23andMers869312889
23andMe allrs869312889
SNP Nexus

SNPshotrs869312889
SNPdbers869312889
MSV3drs869312889
GWAS Ctlgrs869312889
Max Magnitude0
ClinVar
Risk rs869312889(T;T)
Alt rs869312889(T;T)
Reference rs869312889(C;C)
Significance Pathogenic
Disease Autoimmune disease
Variation info
Gene STAT3
CLNDBN Autoimmune disease, multisystem, infantile-onset, 1
Reversed 1
HGVS NC_000017.10:g.40474413G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210428.3,