rs121913387
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121913387(C;T) |
Make rs121913387(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 21971187 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs121913387 |
dbSNP (classic) | rs121913387 |
ClinGen | rs121913387 |
ebi | rs121913387 |
HLI | rs121913387 |
Exac | rs121913387 |
Gnomad | rs121913387 |
Varsome | rs121913387 |
LitVar | rs121913387 |
Map | rs121913387 |
PheGenI | rs121913387 |
Biobank | rs121913387 |
1000 genomes | rs121913387 |
hgdp | rs121913387 |
ensembl | rs121913387 |
geneview | rs121913387 |
scholar | rs121913387 |
rs121913387 | |
pharmgkb | rs121913387 |
gwascentral | rs121913387 |
openSNP | rs121913387 |
23andMe | rs121913387 |
SNPshot | rs121913387 |
SNPdbe | rs121913387 |
MSV3d | rs121913387 |
GWAS Ctlg | rs121913387 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913387(T;T) |
Alt | rs121913387(T;T) |
Reference | Rs121913387(C;C) |
Significance | Probable-Pathogenic |
Disease | Neoplasm |
Variation | info |
Gene | CDKN2A |
CLNDBN | Neoplasm |
Reversed | 1 |
HGVS | NC_000009.11:g.21971186G>A |
CLNSRC | |
CLNACC | RCV000430418.1, |