rs587782388
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587782388(A;A) |
Make rs587782388(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 86899831 |
Gene | BMPR1A |
is a | snp |
is | mentioned by |
dbSNP | rs587782388 |
dbSNP (classic) | rs587782388 |
ClinGen | rs587782388 |
ebi | rs587782388 |
HLI | rs587782388 |
Exac | rs587782388 |
Gnomad | rs587782388 |
Varsome | rs587782388 |
LitVar | rs587782388 |
Map | rs587782388 |
PheGenI | rs587782388 |
Biobank | rs587782388 |
1000 genomes | rs587782388 |
hgdp | rs587782388 |
ensembl | rs587782388 |
geneview | rs587782388 |
scholar | rs587782388 |
rs587782388 | |
pharmgkb | rs587782388 |
gwascentral | rs587782388 |
openSNP | rs587782388 |
23andMe | rs587782388 |
SNPshot | rs587782388 |
SNPdbe | rs587782388 |
MSV3d | rs587782388 |
GWAS Ctlg | rs587782388 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782388(A;A) |
Alt | rs587782388(A;A) |
Reference | Rs587782388(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BMPR1A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.88659588G>A |
CLNSRC | |
CLNACC | RCV000131396.3, |