rs786203662
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GT;GT) | 0 | common in clinvar |
Make rs786203662(C;C) |
Make rs786203662(C;GT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 89971290 |
Gene | NBN |
is a | snp |
is | mentioned by |
dbSNP | rs786203662 |
dbSNP (classic) | rs786203662 |
ClinGen | rs786203662 |
ebi | rs786203662 |
HLI | rs786203662 |
Exac | rs786203662 |
Gnomad | rs786203662 |
Varsome | rs786203662 |
LitVar | rs786203662 |
Map | rs786203662 |
PheGenI | rs786203662 |
Biobank | rs786203662 |
1000 genomes | rs786203662 |
hgdp | rs786203662 |
ensembl | rs786203662 |
geneview | rs786203662 |
scholar | rs786203662 |
rs786203662 | |
pharmgkb | rs786203662 |
gwascentral | rs786203662 |
openSNP | rs786203662 |
23andMe | rs786203662 |
SNPshot | rs786203662 |
SNPdbe | rs786203662 |
MSV3d | rs786203662 |
GWAS Ctlg | rs786203662 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203662(C;C) |
Alt | rs786203662(C;C) |
Reference | Rs786203662(GT;GT) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | NBN |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000008.10:g.90983518_90983519delACinsG |
CLNSRC | |
CLNACC | RCV000167070.1, |