rs180177032
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs180177032(G;T) |
Make rs180177032(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 140781623 |
Gene | BRAF |
is a | snp |
is | mentioned by |
dbSNP | rs180177032 |
dbSNP (classic) | rs180177032 |
ClinGen | rs180177032 |
ebi | rs180177032 |
HLI | rs180177032 |
Exac | rs180177032 |
Gnomad | rs180177032 |
Varsome | rs180177032 |
LitVar | rs180177032 |
Map | rs180177032 |
PheGenI | rs180177032 |
Biobank | rs180177032 |
1000 genomes | rs180177032 |
hgdp | rs180177032 |
ensembl | rs180177032 |
geneview | rs180177032 |
scholar | rs180177032 |
rs180177032 | |
pharmgkb | rs180177032 |
gwascentral | rs180177032 |
openSNP | rs180177032 |
23andMe | rs180177032 |
SNPshot | rs180177032 |
SNPdbe | rs180177032 |
MSV3d | rs180177032 |
GWAS Ctlg | rs180177032 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs180177032(T;T) |
Alt | rs180177032(T;T) |
Reference | Rs180177032(G;G) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | BRAF |
CLNDBN | Carcinoma of colon |
Reversed | 1 |
HGVS | NC_000007.13:g.140481423C>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000014995.6, |