rs137852320

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

154532698

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852320
dbSNP (classic)	rs137852320
ClinGen	rs137852320
ebi	rs137852320
HLI	rs137852320
Exac	rs137852320
Gnomad	rs137852320
Varsome	rs137852320
LitVar	rs137852320
Map	rs137852320
PheGenI	rs137852320
Biobank	rs137852320
1000 genomes	rs137852320
hgdp	rs137852320
ensembl	rs137852320
geneview	rs137852320
scholar	rs137852320
google	rs137852320
pharmgkb	rs137852320
gwascentral	rs137852320
openSNP	rs137852320
23andMe	rs137852320
SNPshot	rs137852320
SNPdbe	rs137852320
MSV3d	rs137852320
GWAS Ctlg	rs137852320

Max Magnitude

5

23andMe name: i5008428

OMIM	305900
Desc
Variant	0012
Related	also

ClinVar
Risk	Rs137852320(G;G)
Alt	Rs137852320(G;G)
Reference	Rs137852320(A;A)
Significance	Other
Disease	G6PD IOWA G6PD IOWA CITY G6PD SPRINGFIELD G6PD WALTER REED Anemia
Variation	info
Gene	G6PD
CLNDBN	G6PD IOWA G6PD IOWA CITY G6PD SPRINGFIELD G6PD WALTER REED Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed	1
HGVS	NC_000023.10:g.153760913T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011096.2, RCV000011097.2, RCV000011098.2, RCV000011099.2, RCV000294855.1,