rs863223537
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 4.3 | Hereditary hemorrhagic telangiectasia |
Make rs863223537(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 127825822 |
Gene | ENG, LOC105379841 |
is a | snp |
is | mentioned by |
dbSNP | rs863223537 |
dbSNP (classic) | rs863223537 |
ClinGen | rs863223537 |
ebi | rs863223537 |
HLI | rs863223537 |
Exac | rs863223537 |
Gnomad | rs863223537 |
Varsome | rs863223537 |
LitVar | rs863223537 |
Map | rs863223537 |
PheGenI | rs863223537 |
Biobank | rs863223537 |
1000 genomes | rs863223537 |
hgdp | rs863223537 |
ensembl | rs863223537 |
geneview | rs863223537 |
scholar | rs863223537 |
rs863223537 | |
pharmgkb | rs863223537 |
gwascentral | rs863223537 |
openSNP | rs863223537 |
23andMe | rs863223537 |
SNPshot | rs863223537 |
SNPdbe | rs863223537 |
MSV3d | rs863223537 |
GWAS Ctlg | rs863223537 |
Max Magnitude | 4.3 |
ClinVar | |
---|---|
Risk | rs863223537(T;T) |
Alt | rs863223537(T;T) |
Reference | Rs863223537(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ENG |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.130588101G>A |
CLNSRC | |
CLNACC | RCV000199857.2, |