rs137852344

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

154532245

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852344
dbSNP (classic)	rs137852344
ClinGen	rs137852344
ebi	rs137852344
HLI	rs137852344
Exac	rs137852344
Gnomad	rs137852344
Varsome	rs137852344
LitVar	rs137852344
Map	rs137852344
PheGenI	rs137852344
Biobank	rs137852344
1000 genomes	rs137852344
hgdp	rs137852344
ensembl	rs137852344
geneview	rs137852344
scholar	rs137852344
google	rs137852344
pharmgkb	rs137852344
gwascentral	rs137852344
openSNP	rs137852344
23andMe	rs137852344
SNPshot	rs137852344
SNPdbe	rs137852344
MSV3d	rs137852344
GWAS Ctlg	rs137852344

Max Magnitude

5

23andMe name: i5008458

OMIM	305900
Desc
Variant	0050
Related	also

ClinVar
Risk	Rs137852344(G;G)
Alt	Rs137852344(G;G)
Reference	Rs137852344(C;C)
Significance	Other
Disease	G6PD NEAPOLIS
Variation	info
Gene	G6PD
CLNDBN	G6PD NEAPOLIS
Reversed	1
HGVS	NC_000023.10:g.153760460G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011152.2,