rs786204195
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;C) | 7 | Pancreatic cancer/Melanoma Syndrome |
(C;C) | 0 | common in clinvar |
Make rs786204195(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 21974686 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs786204195 |
dbSNP (classic) | rs786204195 |
ClinGen | rs786204195 |
ebi | rs786204195 |
HLI | rs786204195 |
Exac | rs786204195 |
Gnomad | rs786204195 |
Varsome | rs786204195 |
LitVar | rs786204195 |
Map | rs786204195 |
PheGenI | rs786204195 |
Biobank | rs786204195 |
1000 genomes | rs786204195 |
hgdp | rs786204195 |
ensembl | rs786204195 |
geneview | rs786204195 |
scholar | rs786204195 |
rs786204195 | |
pharmgkb | rs786204195 |
gwascentral | rs786204195 |
openSNP | rs786204195 |
23andMe | rs786204195 |
SNPshot | rs786204195 |
SNPdbe | rs786204195 |
MSV3d | rs786204195 |
GWAS Ctlg | rs786204195 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs786204195(A;A) rs786204195(T;T) |
Alt | rs786204195(A;A) rs786204195(T;T) |
Reference | Rs786204195(C;C) |
Significance | Pathogenic |
Disease | Hereditary cutaneous melanoma |
Variation | info |
Gene | CDKN2A |
CLNDBN | Hereditary cutaneous melanoma |
Reversed | 1 |
HGVS | NC_000009.11:g.21974685G>T |
CLNSRC | |
CLNACC | RCV000168272.1, |