rs559848002
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs559848002(C;C) |
Make rs559848002(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 21971147 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs559848002 |
dbSNP (classic) | rs559848002 |
ClinGen | rs559848002 |
ebi | rs559848002 |
HLI | rs559848002 |
Exac | rs559848002 |
Gnomad | rs559848002 |
Varsome | rs559848002 |
LitVar | rs559848002 |
Map | rs559848002 |
PheGenI | rs559848002 |
Biobank | rs559848002 |
1000 genomes | rs559848002 |
hgdp | rs559848002 |
ensembl | rs559848002 |
geneview | rs559848002 |
scholar | rs559848002 |
rs559848002 | |
pharmgkb | rs559848002 |
gwascentral | rs559848002 |
openSNP | rs559848002 |
23andMe | rs559848002 |
SNPshot | rs559848002 |
SNPdbe | rs559848002 |
MSV3d | rs559848002 |
GWAS Ctlg | rs559848002 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs559848002(C;C) rs559848002(G;G) |
Alt | rs559848002(C;C) rs559848002(G;G) |
Reference | Rs559848002(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CDKN2A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.21971146T>C |
CLNSRC | |
CLNACC | RCV000478806.1, |