rs730881675
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;ACCCGTGCACGACG) | 7 | Pancreatic cancer/Melanoma Syndrome |
(ACCCGTGCACGACG;ACCCGTGCACGACG) | 0 | common in clinvar |
Make rs730881675(-;-) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 21971106 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs730881675 |
dbSNP (classic) | rs730881675 |
ClinGen | rs730881675 |
ebi | rs730881675 |
HLI | rs730881675 |
Exac | rs730881675 |
Gnomad | rs730881675 |
Varsome | rs730881675 |
LitVar | rs730881675 |
Map | rs730881675 |
PheGenI | rs730881675 |
Biobank | rs730881675 |
1000 genomes | rs730881675 |
hgdp | rs730881675 |
ensembl | rs730881675 |
geneview | rs730881675 |
scholar | rs730881675 |
rs730881675 | |
pharmgkb | rs730881675 |
gwascentral | rs730881675 |
openSNP | rs730881675 |
23andMe | rs730881675 |
SNPshot | rs730881675 |
SNPdbe | rs730881675 |
MSV3d | rs730881675 |
GWAS Ctlg | rs730881675 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs730881675(-;-) |
Alt | rs730881675(-;-) |
Reference | Rs730881675(ACCCGTGCACGACG;ACCCGTGCACGACG) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
Variation | info |
Gene | CDKN2A |
CLNDBN | Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
Reversed | 1 |
HGVS | NC_000009.11:g.21971105_21971118delCGTCGTGCACGGGT |
CLNSRC | |
CLNACC | RCV000160406.1, RCV000458351.1, |