rs121913298
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121913298(A;A) |
Make rs121913298(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 13 |
Position | 48349012 |
Gene | RB1 |
is a | snp |
is | mentioned by |
dbSNP | rs121913298 |
dbSNP (classic) | rs121913298 |
ClinGen | rs121913298 |
ebi | rs121913298 |
HLI | rs121913298 |
Exac | rs121913298 |
Gnomad | rs121913298 |
Varsome | rs121913298 |
LitVar | rs121913298 |
Map | rs121913298 |
PheGenI | rs121913298 |
Biobank | rs121913298 |
1000 genomes | rs121913298 |
hgdp | rs121913298 |
ensembl | rs121913298 |
geneview | rs121913298 |
scholar | rs121913298 |
rs121913298 | |
pharmgkb | rs121913298 |
gwascentral | rs121913298 |
openSNP | rs121913298 |
23andMe | rs121913298 |
SNPshot | rs121913298 |
SNPdbe | rs121913298 |
MSV3d | rs121913298 |
GWAS Ctlg | rs121913298 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913298(A;A) |
Alt | rs121913298(A;A) |
Reference | Rs121913298(T;T) |
Significance | Probable-Pathogenic |
Disease | Retinoblastoma |
Variation | info |
Gene | RB1 |
CLNDBN | Retinoblastoma |
Reversed | 0 |
HGVS | NC_000013.10:g.48923148T>A |
CLNSRC | |
CLNACC | RCV000437633.1, |