rs570278423
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs570278423(C;T) |
Make rs570278423(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 17033077 |
Gene | SDHB |
is a | snp |
is | mentioned by |
dbSNP | rs570278423 |
dbSNP (classic) | rs570278423 |
ClinGen | rs570278423 |
ebi | rs570278423 |
HLI | rs570278423 |
Exac | rs570278423 |
Gnomad | rs570278423 |
Varsome | rs570278423 |
LitVar | rs570278423 |
Map | rs570278423 |
PheGenI | rs570278423 |
Biobank | rs570278423 |
1000 genomes | rs570278423 |
hgdp | rs570278423 |
ensembl | rs570278423 |
geneview | rs570278423 |
scholar | rs570278423 |
rs570278423 | |
pharmgkb | rs570278423 |
gwascentral | rs570278423 |
openSNP | rs570278423 |
23andMe | rs570278423 |
SNPshot | rs570278423 |
SNPdbe | rs570278423 |
MSV3d | rs570278423 |
GWAS Ctlg | rs570278423 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs570278423(T;T) |
Alt | rs570278423(T;T) |
Reference | Rs570278423(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | SDHB |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000001.10:g.17359572C>T |
CLNSRC | |
CLNACC | RCV000492424.1, |