rs863223421
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 6.2 | Pulmonary arterial hypertension |
Make rs863223421(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 202552761 |
Gene | BMPR2 |
is a | snp |
is | mentioned by |
dbSNP | rs863223421 |
dbSNP (classic) | rs863223421 |
ClinGen | rs863223421 |
ebi | rs863223421 |
HLI | rs863223421 |
Exac | rs863223421 |
Gnomad | rs863223421 |
Varsome | rs863223421 |
LitVar | rs863223421 |
Map | rs863223421 |
PheGenI | rs863223421 |
Biobank | rs863223421 |
1000 genomes | rs863223421 |
hgdp | rs863223421 |
ensembl | rs863223421 |
geneview | rs863223421 |
scholar | rs863223421 |
rs863223421 | |
pharmgkb | rs863223421 |
gwascentral | rs863223421 |
openSNP | rs863223421 |
23andMe | rs863223421 |
SNPshot | rs863223421 |
SNPdbe | rs863223421 |
MSV3d | rs863223421 |
GWAS Ctlg | rs863223421 |
Max Magnitude | 6.2 |
ClinVar | |
---|---|
Risk | rs863223421(T;T) |
Alt | rs863223421(T;T) |
Reference | Rs863223421(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | BMPR2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.203417484G>T |
CLNSRC | |
CLNACC | RCV000199780.1, |