rs76645461

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/142

Chromosome

X

Position

154536156

Gene

G6PD

is a	snp
is	mentioned by
dbSNP	rs76645461
dbSNP (classic)	rs76645461
ClinGen	rs76645461
ebi	rs76645461
HLI	rs76645461
Exac	rs76645461
Gnomad	rs76645461
Varsome	rs76645461
LitVar	rs76645461
Map	rs76645461
PheGenI	rs76645461
Biobank	rs76645461
1000 genomes	rs76645461
hgdp	rs76645461
ensembl	rs76645461
geneview	rs76645461
scholar	rs76645461
google	rs76645461
pharmgkb	rs76645461
gwascentral	rs76645461
openSNP	rs76645461
23andMe	rs76645461
SNPshot	rs76645461
SNPdbe	rs76645461
MSV3d	rs76645461
GWAS Ctlg	rs76645461

Max Magnitude

5

OMIM	305900
Desc
Variant	0043
Related	also

ClinVar
Risk	Rs76645461(C;C)
Alt	Rs76645461(C;C)
Reference	Rs76645461(T;T)
Significance	Other
Disease	G6PD AURES not provided
Variation	info
Gene	G6PD
CLNDBN	G6PD AURES not provided
Reversed	1
HGVS	NC_000023.10:g.153764371A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011145.1, RCV000224890.1,