rs786201063
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786201063(A;A) |
Make rs786201063(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 17033059 |
Gene | SDHB |
is a | snp |
is | mentioned by |
dbSNP | rs786201063 |
dbSNP (classic) | rs786201063 |
ClinGen | rs786201063 |
ebi | rs786201063 |
HLI | rs786201063 |
Exac | rs786201063 |
Gnomad | rs786201063 |
Varsome | rs786201063 |
LitVar | rs786201063 |
Map | rs786201063 |
PheGenI | rs786201063 |
Biobank | rs786201063 |
1000 genomes | rs786201063 |
hgdp | rs786201063 |
ensembl | rs786201063 |
geneview | rs786201063 |
scholar | rs786201063 |
rs786201063 | |
pharmgkb | rs786201063 |
gwascentral | rs786201063 |
openSNP | rs786201063 |
23andMe | rs786201063 |
SNPshot | rs786201063 |
SNPdbe | rs786201063 |
MSV3d | rs786201063 |
GWAS Ctlg | rs786201063 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201063(A;A) |
Alt | rs786201063(A;A) |
Reference | Rs786201063(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | SDHB |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000001.10:g.17359554C>T |
CLNSRC | |
CLNACC | RCV000162475.1, |