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

rs869312891

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312891(G;T)
Make rs869312891(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42331524
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312891
ebirs869312891
HLIrs869312891
Exacrs869312891
Varsomers869312891
Maprs869312891
PheGenIrs869312891
hapmaprs869312891
1000 genomesrs869312891
hgdprs869312891
ensemblrs869312891
gopubmedrs869312891
geneviewrs869312891
scholarrs869312891
googlers869312891
pharmgkbrs869312891
gwascentralrs869312891
openSNPrs869312891
23andMers869312891
23andMe allrs869312891
SNP Nexus

SNPshotrs869312891
SNPdbers869312891
MSV3drs869312891
GWAS Ctlgrs869312891
Max Magnitude0
ClinVar
Risk rs869312891(T;T)
Alt rs869312891(T;T)
Reference rs869312891(G;G)
Significance Pathogenic
Disease Autoimmune disease
Variation info
Gene STAT3
CLNDBN Autoimmune disease, multisystem, infantile-onset, 1
Reversed 1
HGVS NC_000017.10:g.40483542C>A
CLNSRC
CLNACC RCV000210422.1,