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rs111033850

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033850(C;C)
Make rs111033850(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position78360132
GeneSOCS3
is asnp
is mentioned by
dbSNPrs111033850
ebirs111033850
HLIrs111033850
Exacrs111033850
Varsomers111033850
Maprs111033850
PheGenIrs111033850
hapmaprs111033850
1000 genomesrs111033850
hgdprs111033850
ensemblrs111033850
gopubmedrs111033850
geneviewrs111033850
scholarrs111033850
googlers111033850
pharmgkbrs111033850
gwascentralrs111033850
openSNPrs111033850
23andMers111033850
23andMe allrs111033850
SNP Nexus

SNPshotrs111033850
SNPdbers111033850
MSV3drs111033850
GWAS Ctlgrs111033850
GMAF0.06015
Max Magnitude0

[PMID 23046072] Mutational Screening of the SOCS3 Gene Promoter in Metastatic Colorectal Cancer Patients

ClinVar
Risk rs111033850(C;C)
Alt rs111033850(C;C)
Reference rs111033850(T;T)
Significance Untested
Disease
Variation info
Gene SOCS3
CLNDBN
Reversed 1
HGVS NC_000017.10:g.76356213A>G
CLNSRC
CLNACC