rs397507481
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397507481(C;G) |
Make rs397507481(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 140754206 |
Gene | BRAF |
is a | snp |
is | mentioned by |
dbSNP | rs397507481 |
dbSNP (classic) | rs397507481 |
ClinGen | rs397507481 |
ebi | rs397507481 |
HLI | rs397507481 |
Exac | rs397507481 |
Gnomad | rs397507481 |
Varsome | rs397507481 |
LitVar | rs397507481 |
Map | rs397507481 |
PheGenI | rs397507481 |
Biobank | rs397507481 |
1000 genomes | rs397507481 |
hgdp | rs397507481 |
ensembl | rs397507481 |
geneview | rs397507481 |
scholar | rs397507481 |
rs397507481 | |
pharmgkb | rs397507481 |
gwascentral | rs397507481 |
openSNP | rs397507481 |
23andMe | rs397507481 |
SNPshot | rs397507481 |
SNPdbe | rs397507481 |
MSV3d | rs397507481 |
GWAS Ctlg | rs397507481 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397507481(A;A) rs397507481(G;G) |
Alt | rs397507481(A;A) rs397507481(G;G) |
Reference | Rs397507481(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | BRAF |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.140454006G>C; NC_000007.13:g.140454006G>T |
CLNSRC | ClinVar |
CLNACC | RCV000033328.3, RCV000157823.1, |