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rs869312887

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312887(C;C)
Make rs869312887(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42333690
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312887
ebirs869312887
HLIrs869312887
Exacrs869312887
Varsomers869312887
Maprs869312887
PheGenIrs869312887
hapmaprs869312887
1000 genomesrs869312887
hgdprs869312887
ensemblrs869312887
gopubmedrs869312887
geneviewrs869312887
scholarrs869312887
googlers869312887
pharmgkbrs869312887
gwascentralrs869312887
openSNPrs869312887
23andMers869312887
23andMe allrs869312887
SNP Nexus

SNPshotrs869312887
SNPdbers869312887
MSV3drs869312887
GWAS Ctlgrs869312887
Max Magnitude0
ClinVar
Risk rs869312887(C;C)
Alt rs869312887(C;C)
Reference rs869312887(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.40485708C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210413.3,