rs137852337

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	5	G6PD deficiency
(G;G)	0	common in clinvar

Reference

GRCh38 38.1/141

Chromosome

X

Position

154532434

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852337
dbSNP (classic)	rs137852337
ClinGen	rs137852337
ebi	rs137852337
HLI	rs137852337
Exac	rs137852337
Gnomad	rs137852337
Varsome	rs137852337
LitVar	rs137852337
Map	rs137852337
PheGenI	rs137852337
Biobank	rs137852337
1000 genomes	rs137852337
hgdp	rs137852337
ensembl	rs137852337
geneview	rs137852337
scholar	rs137852337
google	rs137852337
pharmgkb	rs137852337
gwascentral	rs137852337
openSNP	rs137852337
23andMe	rs137852337
SNPshot	rs137852337
SNPdbe	rs137852337
MSV3d	rs137852337
GWAS Ctlg	rs137852337

Max Magnitude

5

OMIM	305900
Desc
Variant	0040
Related	also

ClinVar
Risk	rs137852337(A;A) Rs137852337(C;C)
Alt	rs137852337(A;A) Rs137852337(C;C)
Reference	Rs137852337(G;G)
Significance	Other
Disease	G6PD PAWNEE Anemia
Variation	info
Gene	G6PD
CLNDBN	G6PD PAWNEE Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed	1
HGVS	NC_000023.10:g.153760649C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011138.4, RCV000011139.7,