rs869025340
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs869025340(C;C) |
Make rs869025340(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 140777032 |
Gene | BRAF |
is a | snp |
is | mentioned by |
dbSNP | rs869025340 |
dbSNP (classic) | rs869025340 |
ClinGen | rs869025340 |
ebi | rs869025340 |
HLI | rs869025340 |
Exac | rs869025340 |
Gnomad | rs869025340 |
Varsome | rs869025340 |
LitVar | rs869025340 |
Map | rs869025340 |
PheGenI | rs869025340 |
Biobank | rs869025340 |
1000 genomes | rs869025340 |
hgdp | rs869025340 |
ensembl | rs869025340 |
geneview | rs869025340 |
scholar | rs869025340 |
rs869025340 | |
pharmgkb | rs869025340 |
gwascentral | rs869025340 |
openSNP | rs869025340 |
23andMe | rs869025340 |
SNPshot | rs869025340 |
SNPdbe | rs869025340 |
MSV3d | rs869025340 |
GWAS Ctlg | rs869025340 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025340(C;C) rs869025340(G;G) |
Alt | rs869025340(C;C) rs869025340(G;G) |
Reference | Rs869025340(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | BRAF |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.140476832A>C; NC_000007.13:g.140476832A>G |
CLNSRC | |
CLNACC | RCV000413915.1, RCV000207510.1, |