rs879254290
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs879254290(-;C) |
Make rs879254290(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 8 |
Position | 133250456 |
Gene | NDRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs879254290 |
dbSNP (classic) | rs879254290 |
ClinGen | rs879254290 |
ebi | rs879254290 |
HLI | rs879254290 |
Exac | rs879254290 |
Gnomad | rs879254290 |
Varsome | rs879254290 |
LitVar | rs879254290 |
Map | rs879254290 |
PheGenI | rs879254290 |
Biobank | rs879254290 |
1000 genomes | rs879254290 |
hgdp | rs879254290 |
ensembl | rs879254290 |
geneview | rs879254290 |
scholar | rs879254290 |
rs879254290 | |
pharmgkb | rs879254290 |
gwascentral | rs879254290 |
openSNP | rs879254290 |
23andMe | rs879254290 |
SNPshot | rs879254290 |
SNPdbe | rs879254290 |
MSV3d | rs879254290 |
GWAS Ctlg | rs879254290 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879254290(C;C) |
Alt | rs879254290(C;C) |
Reference | Rs879254290(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDRG1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000008.10:g.134262700dupG |
CLNSRC | |
CLNACC | RCV000236853.2, |