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rs587777649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777649(C;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position42322445
GeneSTAT3
is asnp
is mentioned by
dbSNPrs587777649
ebirs587777649
HLIrs587777649
Exacrs587777649
Varsomers587777649
Maprs587777649
PheGenIrs587777649
hapmaprs587777649
1000 genomesrs587777649
hgdprs587777649
ensemblrs587777649
gopubmedrs587777649
geneviewrs587777649
scholarrs587777649
googlers587777649
pharmgkbrs587777649
gwascentralrs587777649
openSNPrs587777649
23andMers587777649
23andMe allrs587777649
SNP Nexus

SNPshotrs587777649
SNPdbers587777649
MSV3drs587777649
GWAS Ctlgrs587777649
Max Magnitude0
ClinVar
Risk rs587777649(G;G)
Alt rs587777649(G;G)
Reference rs587777649(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.40474463G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133538.3,