rs137852746
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6.2 | Pulmonary arterial hypertension |
Make rs137852746(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 202552773 |
Gene | BMPR2 |
is a | snp |
is | mentioned by |
dbSNP | rs137852746 |
dbSNP (classic) | rs137852746 |
ClinGen | rs137852746 |
ebi | rs137852746 |
HLI | rs137852746 |
Exac | rs137852746 |
Gnomad | rs137852746 |
Varsome | rs137852746 |
LitVar | rs137852746 |
Map | rs137852746 |
PheGenI | rs137852746 |
Biobank | rs137852746 |
1000 genomes | rs137852746 |
hgdp | rs137852746 |
ensembl | rs137852746 |
geneview | rs137852746 |
scholar | rs137852746 |
rs137852746 | |
pharmgkb | rs137852746 |
gwascentral | rs137852746 |
openSNP | rs137852746 |
23andMe | rs137852746 |
SNPshot | rs137852746 |
SNPdbe | rs137852746 |
MSV3d | rs137852746 |
GWAS Ctlg | rs137852746 |
Max Magnitude | 6.2 |
aka c.1471C>T (p.Arg491Trp)
23andMe name: i5005632
ClinVar | |
---|---|
Risk | rs137852746(T;T) |
Alt | rs137852746(T;T) |
Reference | Rs137852746(C;C) |
Significance | Pathogenic |
Disease | Primary pulmonary hypertension not provided |
Variation | info |
Gene | BMPR2 |
CLNDBN | Primary pulmonary hypertension not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.203417496C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000009347.4, RCV000493405.1, |