rs111033850
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs111033850(C;C) |
Make rs111033850(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 78360132 |
Gene | LOC101928674, SOCS3 |
is a | snp |
is | mentioned by |
dbSNP | rs111033850 |
dbSNP (classic) | rs111033850 |
ClinGen | rs111033850 |
ebi | rs111033850 |
HLI | rs111033850 |
Exac | rs111033850 |
Gnomad | rs111033850 |
Varsome | rs111033850 |
LitVar | rs111033850 |
Map | rs111033850 |
PheGenI | rs111033850 |
Biobank | rs111033850 |
1000 genomes | rs111033850 |
hgdp | rs111033850 |
ensembl | rs111033850 |
geneview | rs111033850 |
scholar | rs111033850 |
rs111033850 | |
pharmgkb | rs111033850 |
gwascentral | rs111033850 |
openSNP | rs111033850 |
23andMe | rs111033850 |
SNPshot | rs111033850 |
SNPdbe | rs111033850 |
MSV3d | rs111033850 |
GWAS Ctlg | rs111033850 |
GMAF | 0.06015 |
Max Magnitude | 0 |
[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 |