rs17878459
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | CYP2C19*2B homozygote | |
(C;G) | carrier of one CYP2C19*2B allele | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 94775165 |
Gene | CYP2C19 |
is a | snp |
is | mentioned by |
dbSNP | rs17878459 |
dbSNP (classic) | rs17878459 |
ClinGen | rs17878459 |
ebi | rs17878459 |
HLI | rs17878459 |
Exac | rs17878459 |
Gnomad | rs17878459 |
Varsome | rs17878459 |
LitVar | rs17878459 |
Map | rs17878459 |
PheGenI | rs17878459 |
Biobank | rs17878459 |
1000 genomes | rs17878459 |
hgdp | rs17878459 |
ensembl | rs17878459 |
geneview | rs17878459 |
scholar | rs17878459 |
rs17878459 | |
pharmgkb | rs17878459 |
gwascentral | rs17878459 |
openSNP | rs17878459 |
23andMe | rs17878459 |
SNPshot | rs17878459 |
SNPdbe | rs17878459 |
MSV3d | rs17878459 |
GWAS Ctlg | rs17878459 |
GMAF | 0.01653 |
Max Magnitude | 0 |
The rs17878459(C) SNP defines the CYP2C19 allele known as CYP2C19*2B, or as E92D.[PMID 9732415]
ClinVar | |
---|---|
Risk | rs17878459(A;A) Rs17878459(C;C) |
Alt | rs17878459(A;A) Rs17878459(C;C) |
Reference | Rs17878459(G;G) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | CYP2C19 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000010.11:g.94775165G>A |
CLNSRC | ClinVar |
CLNACC | RCV000069096.2, |