rs180177033
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs180177033(G;G) |
Make rs180177033(G;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 140781620 |
Gene | BRAF |
is a | snp |
is | mentioned by |
dbSNP | rs180177033 |
dbSNP (classic) | rs180177033 |
ClinGen | rs180177033 |
ebi | rs180177033 |
HLI | rs180177033 |
Exac | rs180177033 |
Gnomad | rs180177033 |
Varsome | rs180177033 |
LitVar | rs180177033 |
Map | rs180177033 |
PheGenI | rs180177033 |
Biobank | rs180177033 |
1000 genomes | rs180177033 |
hgdp | rs180177033 |
ensembl | rs180177033 |
geneview | rs180177033 |
scholar | rs180177033 |
rs180177033 | |
pharmgkb | rs180177033 |
gwascentral | rs180177033 |
openSNP | rs180177033 |
23andMe | rs180177033 |
SNPshot | rs180177033 |
SNPdbe | rs180177033 |
MSV3d | rs180177033 |
GWAS Ctlg | rs180177033 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs180177033(G;G) |
Alt | rs180177033(G;G) |
Reference | Rs180177033(T;T) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | BRAF |
CLNDBN | Carcinoma of colon |
Reversed | 1 |
HGVS | NC_000007.13:g.140481420A>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000014996.6, |