rs587781928
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs587781928(-;-) |
Make rs587781928(-;GA) |
Make rs587781928(GA;GA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 86917284 |
Gene | BMPR1A |
is a | snp |
is | mentioned by |
dbSNP | rs587781928 |
dbSNP (classic) | rs587781928 |
ClinGen | rs587781928 |
ebi | rs587781928 |
HLI | rs587781928 |
Exac | rs587781928 |
Gnomad | rs587781928 |
Varsome | rs587781928 |
LitVar | rs587781928 |
Map | rs587781928 |
PheGenI | rs587781928 |
Biobank | rs587781928 |
1000 genomes | rs587781928 |
hgdp | rs587781928 |
ensembl | rs587781928 |
geneview | rs587781928 |
scholar | rs587781928 |
rs587781928 | |
pharmgkb | rs587781928 |
gwascentral | rs587781928 |
openSNP | rs587781928 |
23andMe | rs587781928 |
SNPshot | rs587781928 |
SNPdbe | rs587781928 |
MSV3d | rs587781928 |
GWAS Ctlg | rs587781928 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781928(-;-) |
Alt | rs587781928(-;-) |
Reference | Rs587781928(AG;AG) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BMPR1A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.88677041_88677042delGA |
CLNSRC | |
CLNACC | RCV000130286.2, |