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rs869312894

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312894(A;A)
Make rs869312894(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position42317219
GeneSTAT3
is asnp
is mentioned by
dbSNPrs869312894
ebirs869312894
HLIrs869312894
Exacrs869312894
Varsomers869312894
Maprs869312894
PheGenIrs869312894
hapmaprs869312894
1000 genomesrs869312894
hgdprs869312894
ensemblrs869312894
gopubmedrs869312894
geneviewrs869312894
scholarrs869312894
googlers869312894
pharmgkbrs869312894
gwascentralrs869312894
openSNPrs869312894
23andMers869312894
23andMe allrs869312894
SNP Nexus

SNPshotrs869312894
SNPdbers869312894
MSV3drs869312894
GWAS Ctlgrs869312894
Max Magnitude0
ClinVar
Risk rs869312894(A;A)
Alt rs869312894(A;A)
Reference rs869312894(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.40469237C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210433.2,