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rs869312890

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312890(C;T)
Make rs869312890(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42339328
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312890
ebirs869312890
HLIrs869312890
Exacrs869312890
Varsomers869312890
Maprs869312890
PheGenIrs869312890
hapmaprs869312890
1000 genomesrs869312890
hgdprs869312890
ensemblrs869312890
gopubmedrs869312890
geneviewrs869312890
scholarrs869312890
googlers869312890
pharmgkbrs869312890
gwascentralrs869312890
openSNPrs869312890
23andMers869312890
23andMe allrs869312890
SNP Nexus

SNPshotrs869312890
SNPdbers869312890
MSV3drs869312890
GWAS Ctlgrs869312890
Max Magnitude0
ClinVar
Risk rs869312890(T;T)
Alt rs869312890(T;T)
Reference rs869312890(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.40491346G>A
CLNSRC
CLNACC RCV000210417.1,