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rs786205503

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205503(G;T)
Make rs786205503(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position42323024
GeneSTAT3
is asnp
is mentioned by
dbSNPrs786205503
ebirs786205503
HLIrs786205503
Exacrs786205503
Varsomers786205503
Maprs786205503
PheGenIrs786205503
hapmaprs786205503
1000 genomesrs786205503
hgdprs786205503
ensemblrs786205503
gopubmedrs786205503
geneviewrs786205503
scholarrs786205503
googlers786205503
pharmgkbrs786205503
gwascentralrs786205503
openSNPrs786205503
23andMers786205503
23andMe allrs786205503
SNP Nexus

SNPshotrs786205503
SNPdbers786205503
MSV3drs786205503
GWAS Ctlgrs786205503
Max Magnitude0
ClinVar
Risk rs786205503(T;T)
Alt rs786205503(T;T)
Reference rs786205503(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40475042C>A
CLNSRC
CLNACC RCV000171258.1,