rs137852326

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	3	Carrier of G6PD deficiency mutation; variable expressivity
(T;T)	5	G6PD deficiency

Reference

GRCh38 38.1/141

Chromosome

X

Position

154534345

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852326
dbSNP (classic)	rs137852326
ClinGen	rs137852326
ebi	rs137852326
HLI	rs137852326
Exac	rs137852326
Gnomad	rs137852326
Varsome	rs137852326
LitVar	rs137852326
Map	rs137852326
PheGenI	rs137852326
Biobank	rs137852326
1000 genomes	rs137852326
hgdp	rs137852326
ensembl	rs137852326
geneview	rs137852326
scholar	rs137852326
google	rs137852326
pharmgkb	rs137852326
gwascentral	rs137852326
openSNP	rs137852326
23andMe	rs137852326
SNPshot	rs137852326
SNPdbe	rs137852326
MSV3d	rs137852326
GWAS Ctlg	rs137852326

Max Magnitude

5

OMIM	305900
Desc
Variant	0024
Related	also

ClinVar
Risk	rs137852326(C;C) Rs137852326(T;T)
Alt	rs137852326(C;C) Rs137852326(T;T)
Reference	Rs137852326(G;G)
Significance	Other
Disease	G6PD GASTONIA G6PD MARION G6PD MINNESOTA Anemia not provided
Variation	info
Gene	G6PD
CLNDBN	G6PD GASTONIA G6PD MARION G6PD MINNESOTA Anemia, nonspherocytic hemolytic, due to G6PD deficiency not provided
Reversed	1
HGVS	NC_000023.10:g.153762560C>A
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000011110.3, RCV000011111.3, RCV000011112.3, RCV000066251.6, RCV000079410.3,