rs876659988
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs876659988(A;GTTCATAGCGG) |
Make rs876659988(GTTCATAGCGG;GTTCATAGCGG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 86919187 |
Gene | BMPR1A |
is a | snp |
is | mentioned by |
dbSNP | rs876659988 |
dbSNP (classic) | rs876659988 |
ClinGen | rs876659988 |
ebi | rs876659988 |
HLI | rs876659988 |
Exac | rs876659988 |
Gnomad | rs876659988 |
Varsome | rs876659988 |
LitVar | rs876659988 |
Map | rs876659988 |
PheGenI | rs876659988 |
Biobank | rs876659988 |
1000 genomes | rs876659988 |
hgdp | rs876659988 |
ensembl | rs876659988 |
geneview | rs876659988 |
scholar | rs876659988 |
rs876659988 | |
pharmgkb | rs876659988 |
gwascentral | rs876659988 |
openSNP | rs876659988 |
23andMe | rs876659988 |
SNPshot | rs876659988 |
SNPdbe | rs876659988 |
MSV3d | rs876659988 |
GWAS Ctlg | rs876659988 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876659988(GTTCATAGCGG;GTTCATAGCGG) |
Alt | rs876659988(GTTCATAGCGG;GTTCATAGCGG) |
Reference | Rs876659988(A;A) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BMPR1A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.88678944delAinsGTTCATAGCGG |
CLNSRC | |
CLNACC | RCV000222176.1, |