rs730881672
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;CT) | 7 | Pancreatic cancer/Melanoma Syndrome |
Make rs730881672(-;GGC) |
Make rs730881672(GGC;GGC) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 21974781 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs730881672 |
dbSNP (classic) | rs730881672 |
ClinGen | rs730881672 |
ebi | rs730881672 |
HLI | rs730881672 |
Exac | rs730881672 |
Gnomad | rs730881672 |
Varsome | rs730881672 |
LitVar | rs730881672 |
Map | rs730881672 |
PheGenI | rs730881672 |
Biobank | rs730881672 |
1000 genomes | rs730881672 |
hgdp | rs730881672 |
ensembl | rs730881672 |
geneview | rs730881672 |
scholar | rs730881672 |
rs730881672 | |
pharmgkb | rs730881672 |
gwascentral | rs730881672 |
openSNP | rs730881672 |
23andMe | rs730881672 |
SNPshot | rs730881672 |
SNPdbe | rs730881672 |
MSV3d | rs730881672 |
GWAS Ctlg | rs730881672 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs730881672(GGC;GGC) |
Alt | rs730881672(GGC;GGC) |
Reference | Rs730881672(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | CDKN2A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000009.11:g.21974780_21974781insGCC |
CLNSRC | |
CLNACC | RCV000160402.1, |