rs137854599
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs137854599(A;A) |
Make rs137854599(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 21971093 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs137854599 |
dbSNP (classic) | rs137854599 |
ClinGen | rs137854599 |
ebi | rs137854599 |
HLI | rs137854599 |
Exac | rs137854599 |
Gnomad | rs137854599 |
Varsome | rs137854599 |
LitVar | rs137854599 |
Map | rs137854599 |
PheGenI | rs137854599 |
Biobank | rs137854599 |
1000 genomes | rs137854599 |
hgdp | rs137854599 |
ensembl | rs137854599 |
geneview | rs137854599 |
scholar | rs137854599 |
rs137854599 | |
pharmgkb | rs137854599 |
gwascentral | rs137854599 |
openSNP | rs137854599 |
23andMe | rs137854599 |
SNPshot | rs137854599 |
SNPdbe | rs137854599 |
MSV3d | rs137854599 |
GWAS Ctlg | rs137854599 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854599(A;A) |
Alt | rs137854599(A;A) |
Reference | Rs137854599(G;G) |
Significance | Other |
Disease | Melanoma Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | CDKN2A |
CLNDBN | Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.21971092C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000010033.2, RCV000122946.1, RCV000219725.2, RCV000493646.1, |