rs587781720
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587781720(C;T) |
Make rs587781720(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 230923 |
Gene | SDHA |
is a | snp |
is | mentioned by |
dbSNP | rs587781720 |
dbSNP (classic) | rs587781720 |
ClinGen | rs587781720 |
ebi | rs587781720 |
HLI | rs587781720 |
Exac | rs587781720 |
Gnomad | rs587781720 |
Varsome | rs587781720 |
LitVar | rs587781720 |
Map | rs587781720 |
PheGenI | rs587781720 |
Biobank | rs587781720 |
1000 genomes | rs587781720 |
hgdp | rs587781720 |
ensembl | rs587781720 |
geneview | rs587781720 |
scholar | rs587781720 |
rs587781720 | |
pharmgkb | rs587781720 |
gwascentral | rs587781720 |
openSNP | rs587781720 |
23andMe | rs587781720 |
SNPshot | rs587781720 |
SNPdbe | rs587781720 |
MSV3d | rs587781720 |
GWAS Ctlg | rs587781720 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781720(T;T) |
Alt | rs587781720(T;T) |
Reference | Rs587781720(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Paragangliomas 5 |
Variation | info |
Gene | SDHA |
CLNDBN | Hereditary cancer-predisposing syndrome Paragangliomas 5 |
Reversed | 0 |
HGVS | NC_000005.9:g.231038C>T |
CLNSRC | |
CLNACC | RCV000129906.2, RCV000409578.1, |