rs36204594
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;C) | 7 | Pancreatic cancer/Melanoma Syndrome |
(C;C) | 0 | common in clinvar |
Make rs36204594(C;T) |
Make rs36204594(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 21971180 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs36204594 |
dbSNP (classic) | rs36204594 |
ClinGen | rs36204594 |
ebi | rs36204594 |
HLI | rs36204594 |
Exac | rs36204594 |
Gnomad | rs36204594 |
Varsome | rs36204594 |
LitVar | rs36204594 |
Map | rs36204594 |
PheGenI | rs36204594 |
Biobank | rs36204594 |
1000 genomes | rs36204594 |
hgdp | rs36204594 |
ensembl | rs36204594 |
geneview | rs36204594 |
scholar | rs36204594 |
rs36204594 | |
pharmgkb | rs36204594 |
gwascentral | rs36204594 |
openSNP | rs36204594 |
23andMe | rs36204594 |
SNPshot | rs36204594 |
SNPdbe | rs36204594 |
MSV3d | rs36204594 |
GWAS Ctlg | rs36204594 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs36204594(A;A) |
Alt | rs36204594(A;A) |
Reference | Rs36204594(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | CDKN2A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000009.11:g.21971179G>T |
CLNSRC | |
CLNACC | RCV000165798.1, |