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rs869312892

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312892(C;T)
Make rs869312892(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42316899
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312892
ebirs869312892
HLIrs869312892
Exacrs869312892
Varsomers869312892
Maprs869312892
PheGenIrs869312892
hapmaprs869312892
1000 genomesrs869312892
hgdprs869312892
ensemblrs869312892
gopubmedrs869312892
geneviewrs869312892
scholarrs869312892
googlers869312892
pharmgkbrs869312892
gwascentralrs869312892
openSNPrs869312892
23andMers869312892
23andMe allrs869312892
SNP Nexus

SNPshotrs869312892
SNPdbers869312892
MSV3drs869312892
GWAS Ctlgrs869312892
Max Magnitude0
ClinVar
Risk rs869312892(T;T)
Alt rs869312892(T;T)
Reference rs869312892(C;C)
Significance Pathogenic
Disease Autoimmune disease not provided
Variation info
Gene STAT3
CLNDBN Autoimmune disease, multisystem, infantile-onset, 1 not provided
Reversed 1
HGVS NC_000017.10:g.40468917G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210415.3, RCV000224259.1,