rs768378152
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TC;TC) | 0 | common in clinvar |
Make rs768378152(-;-) |
Make rs768378152(-;TC) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 89981513 |
Gene | NBN |
is a | snp |
is | mentioned by |
dbSNP | rs768378152 |
dbSNP (classic) | rs768378152 |
ClinGen | rs768378152 |
ebi | rs768378152 |
HLI | rs768378152 |
Exac | rs768378152 |
Gnomad | rs768378152 |
Varsome | rs768378152 |
LitVar | rs768378152 |
Map | rs768378152 |
PheGenI | rs768378152 |
Biobank | rs768378152 |
1000 genomes | rs768378152 |
hgdp | rs768378152 |
ensembl | rs768378152 |
geneview | rs768378152 |
scholar | rs768378152 |
rs768378152 | |
pharmgkb | rs768378152 |
gwascentral | rs768378152 |
openSNP | rs768378152 |
23andMe | rs768378152 |
SNPshot | rs768378152 |
SNPdbe | rs768378152 |
MSV3d | rs768378152 |
GWAS Ctlg | rs768378152 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768378152(-;-) |
Alt | rs768378152(-;-) |
Reference | Rs768378152(TC;TC) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | NBN |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000008.10:g.90993741_90993742delTC |
CLNSRC | |
CLNACC | RCV000166151.1, |