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rs869312888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312888(A;A)
Make rs869312888(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42329430
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312888
dbSNP (old)rs869312888
ClinGenrs869312888
ebirs869312888
HLIrs869312888
Exacrs869312888
Varsomers869312888
Maprs869312888
PheGenIrs869312888
Biobankrs869312888
1000 genomesrs869312888
hgdprs869312888
ensemblrs869312888
gopubmedrs869312888
geneviewrs869312888
scholarrs869312888
googlers869312888
pharmgkbrs869312888
gwascentralrs869312888
openSNPrs869312888
23andMers869312888
23andMe allrs869312888
SNP Nexus

SNPshotrs869312888
SNPdbers869312888
MSV3drs869312888
GWAS Ctlgrs869312888
Max Magnitude0
ClinVar
Risk rs869312888(A;A)
Alt rs869312888(A;A)
Reference Rs869312888(G;G)
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.40481448C>T
CLNSRC
CLNACC RCV000210420.1, RCV000489679.1,