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rs1085307931

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position42333730
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1085307931
dbSNP (old)rs1085307931
ClinGenrs1085307931
ebirs1085307931
HLIrs1085307931
Exacrs1085307931
Gnomadrs1085307931
Varsomers1085307931
Maprs1085307931
PheGenIrs1085307931
Biobankrs1085307931
1000 genomesrs1085307931
hgdprs1085307931
ensemblrs1085307931
gopubmedrs1085307931
geneviewrs1085307931
scholarrs1085307931
googlers1085307931
pharmgkbrs1085307931
gwascentralrs1085307931
openSNPrs1085307931
23andMers1085307931
23andMe allrs1085307931
SNPshotrs1085307931
SNPdbers1085307931
MSV3drs1085307931
GWAS Ctlgrs1085307931
Max Magnitude0
ClinVar
Risk rs1085307931(G;G)
Alt rs1085307931(G;G)
Reference Rs1085307931(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40485748A>C
CLNSRC
CLNACC RCV000488939.1,