rs17878459

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
google	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,