rs137852314

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

154534495

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852314
dbSNP (classic)	rs137852314
ClinGen	rs137852314
ebi	rs137852314
HLI	rs137852314
Exac	rs137852314
Gnomad	rs137852314
Varsome	rs137852314
LitVar	rs137852314
Map	rs137852314
PheGenI	rs137852314
Biobank	rs137852314
1000 genomes	rs137852314
hgdp	rs137852314
ensembl	rs137852314
geneview	rs137852314
scholar	rs137852314
google	rs137852314
pharmgkb	rs137852314
gwascentral	rs137852314
openSNP	rs137852314
23andMe	rs137852314
SNPshot	rs137852314
SNPdbe	rs137852314
MSV3d	rs137852314
GWAS Ctlg	rs137852314

Max Magnitude

5

23andMe name: i5008421

OMIM	305900
Desc
Variant	0005
Related	also

ClinVar
Risk	Rs137852314(A;A)
Alt	Rs137852314(A;A)
Reference	Rs137852314(G;G)
Significance	Other
Disease	G6PD MAHIDOL Anemia
Variation	info
Gene	G6PD
CLNDBN	G6PD MAHIDOL Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed	1
HGVS	NC_000023.10:g.153762710C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011085.3, RCV000282708.1,