rs11552822
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11552822(G;T) |
Make rs11552822(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 21971109 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs11552822 |
dbSNP (classic) | rs11552822 |
ClinGen | rs11552822 |
ebi | rs11552822 |
HLI | rs11552822 |
Exac | rs11552822 |
Gnomad | rs11552822 |
Varsome | rs11552822 |
LitVar | rs11552822 |
Map | rs11552822 |
PheGenI | rs11552822 |
Biobank | rs11552822 |
1000 genomes | rs11552822 |
hgdp | rs11552822 |
ensembl | rs11552822 |
geneview | rs11552822 |
scholar | rs11552822 |
rs11552822 | |
pharmgkb | rs11552822 |
gwascentral | rs11552822 |
openSNP | rs11552822 |
23andMe | rs11552822 |
SNPshot | rs11552822 |
SNPdbe | rs11552822 |
MSV3d | rs11552822 |
GWAS Ctlg | rs11552822 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11552822(A;A) rs11552822(T;T) |
Alt | rs11552822(A;A) rs11552822(T;T) |
Reference | Rs11552822(G;G) |
Significance | Probable-Pathogenic |
Disease | Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
Variation | info |
Gene | CDKN2A |
CLNDBN | Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
Reversed | 1 |
HGVS | NC_000009.11:g.21971108C>A; NC_000009.11:g.21971108C>T |
CLNSRC | |
CLNACC | RCV000419046.1, RCV000214736.1, RCV000474240.1, |