rs137852334

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

154532695

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852334
dbSNP (classic)	rs137852334
ClinGen	rs137852334
ebi	rs137852334
HLI	rs137852334
Exac	rs137852334
Gnomad	rs137852334
Varsome	rs137852334
LitVar	rs137852334
Map	rs137852334
PheGenI	rs137852334
Biobank	rs137852334
1000 genomes	rs137852334
hgdp	rs137852334
ensembl	rs137852334
geneview	rs137852334
scholar	rs137852334
google	rs137852334
pharmgkb	rs137852334
gwascentral	rs137852334
openSNP	rs137852334
23andMe	rs137852334
SNPshot	rs137852334
SNPdbe	rs137852334
MSV3d	rs137852334
GWAS Ctlg	rs137852334

Max Magnitude

5

23andMe name: i5008446

OMIM	305900
Desc
Variant	0037
Related	also

ClinVar
Risk	Rs137852334(T;T)
Alt	Rs137852334(T;T)
Reference	Rs137852334(C;C)
Significance	Other
Disease	G6PD GUADALAJARA Anemia
Variation	info
Gene	G6PD
CLNDBN	G6PD GUADALAJARA Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed	1
HGVS	NC_000023.10:g.153760910G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011132.3, RCV000011133.7,