rs137852341

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

154535261

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs137852341
dbSNP (classic)	rs137852341
ClinGen	rs137852341
ebi	rs137852341
HLI	rs137852341
Exac	rs137852341
Gnomad	rs137852341
Varsome	rs137852341
LitVar	rs137852341
Map	rs137852341
PheGenI	rs137852341
Biobank	rs137852341
1000 genomes	rs137852341
hgdp	rs137852341
ensembl	rs137852341
geneview	rs137852341
scholar	rs137852341
google	rs137852341
pharmgkb	rs137852341
gwascentral	rs137852341
openSNP	rs137852341
23andMe	rs137852341
SNPshot	rs137852341
SNPdbe	rs137852341
MSV3d	rs137852341
GWAS Ctlg	rs137852341

GMAF

0.0006046

Max Magnitude

5

OMIM	305900
Desc
Variant	0045
Related	also

ClinVar
Risk	rs137852341(A;A) Rs137852341(T;T)
Alt	rs137852341(A;A) Rs137852341(T;T)
Reference	Rs137852341(G;G)
Significance	Other
Disease	G6PD QUING YUAN
Variation	info
Gene	G6PD
CLNDBN	G6PD QUING YUAN
Reversed	1
HGVS	NC_000023.10:g.153763476C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011147.1,