rs915909

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	normal
(C;T)		carrier of one CYP2E1_6498C>T(I321I) allele
(G;G)	0
(T;T)	0	CYP2E1_6498C>T(I321I) homozygote

Reference

GRCh38 38.1/142

Chromosome

10

Position

133533893

Gene

CYP2E1

is a	snp
is	mentioned by
dbSNP	rs915909
dbSNP (classic)	rs915909
ClinGen	rs915909
ebi	rs915909
HLI	rs915909
Exac	rs915909
Gnomad	rs915909
Varsome	rs915909
LitVar	rs915909
Map	rs915909
PheGenI	rs915909
Biobank	rs915909
1000 genomes	rs915909
hgdp	rs915909
ensembl	rs915909
geneview	rs915909
scholar	rs915909
google	rs915909
pharmgkb	rs915909
gwascentral	rs915909
openSNP	rs915909
23andMe	rs915909
SNPshot	rs915909
SNPdbe	rs915909
MSV3d	rs915909
GWAS Ctlg	rs915909

GMAF

0.02663

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

rs915909 is a SNP in the CYP2E1 gene.

The rs915909(T) allele defines the CYP2E1_6498C>T(I321I) variant.

[PMID 18663376] Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene.

ClinVar
Risk	Rs915909(C;C)
Alt	Rs915909(C;C)
Reference	Rs915909(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	CYP2E1
CLNDBN	not specified
Reversed	0
HGVS	NC_000010.10:g.135347397T>C
CLNSRC
CLNACC	RCV000455117.1,