rs137852327

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

154533122

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852327
dbSNP (classic)	rs137852327
ClinGen	rs137852327
ebi	rs137852327
HLI	rs137852327
Exac	rs137852327
Gnomad	rs137852327
Varsome	rs137852327
LitVar	rs137852327
Map	rs137852327
PheGenI	rs137852327
Biobank	rs137852327
1000 genomes	rs137852327
hgdp	rs137852327
ensembl	rs137852327
geneview	rs137852327
scholar	rs137852327
google	rs137852327
pharmgkb	rs137852327
gwascentral	rs137852327
openSNP	rs137852327
23andMe	rs137852327
SNPshot	rs137852327
SNPdbe	rs137852327
MSV3d	rs137852327
GWAS Ctlg	rs137852327

Max Magnitude

5

23andMe name: i5008436

OMIM	305900
Desc
Variant	0026
Related	also

ClinVar
Risk	Rs137852327(A;A)
Alt	Rs137852327(A;A)
Reference	Rs137852327(G;G)
Significance	Other
Disease	G6PD VIANGCHAN G6PD JAMMU not provided Anemia Glucose 6 phosphate dehydrogenase deficiency
Variation	info
Gene	G6PD
CLNDBN	G6PD VIANGCHAN G6PD JAMMU not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency Glucose 6 phosphate dehydrogenase deficiency
Reversed	1
HGVS	NC_000023.10:g.153761337C>T
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000011116.3, RCV000011117.3, RCV000079415.3, RCV000180545.2, RCV000405688.1,