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rs587777647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777647(A;A)
Make rs587777647(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position42316896
GeneSTAT3
is asnp
is mentioned by
dbSNPrs587777647
ebirs587777647
HLIrs587777647
Exacrs587777647
Varsomers587777647
Maprs587777647
PheGenIrs587777647
hapmaprs587777647
1000 genomesrs587777647
hgdprs587777647
ensemblrs587777647
gopubmedrs587777647
geneviewrs587777647
scholarrs587777647
googlers587777647
pharmgkbrs587777647
gwascentralrs587777647
openSNPrs587777647
23andMers587777647
23andMe allrs587777647
SNP Nexus

SNPshotrs587777647
SNPdbers587777647
MSV3drs587777647
GWAS Ctlgrs587777647
Max Magnitude0
ClinVar
Risk rs587777647(A;A)
Alt rs587777647(A;A)
Reference rs587777647(G;G)
Significance Pathogenic
Disease Autoimmune disease
Variation info
Gene STAT3
CLNDBN Autoimmune disease, multisystem, infantile-onset
Reversed 0
HGVS NC_000017.11:g.42316896G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133536.1,