rs876659592
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs876659592(-;-) |
Make rs876659592(-;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 8 |
Position | 89981507 |
Gene | NBN |
is a | snp |
is | mentioned by |
dbSNP | rs876659592 |
dbSNP (classic) | rs876659592 |
ClinGen | rs876659592 |
ebi | rs876659592 |
HLI | rs876659592 |
Exac | rs876659592 |
Gnomad | rs876659592 |
Varsome | rs876659592 |
LitVar | rs876659592 |
Map | rs876659592 |
PheGenI | rs876659592 |
Biobank | rs876659592 |
1000 genomes | rs876659592 |
hgdp | rs876659592 |
ensembl | rs876659592 |
geneview | rs876659592 |
scholar | rs876659592 |
rs876659592 | |
pharmgkb | rs876659592 |
gwascentral | rs876659592 |
openSNP | rs876659592 |
23andMe | rs876659592 |
SNPshot | rs876659592 |
SNPdbe | rs876659592 |
MSV3d | rs876659592 |
GWAS Ctlg | rs876659592 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876659592(-;-) |
Alt | rs876659592(-;-) |
Reference | Rs876659592(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | NBN |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000008.10:g.90993735delA |
CLNSRC | |
CLNACC | RCV000221586.1, |