rs151344482

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs151344482(A;G)

Make rs151344482(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

37796093

Gene

CYBB

is a	snp
is	mentioned by
dbSNP	rs151344482
dbSNP (classic)	rs151344482
ClinGen	rs151344482
ebi	rs151344482
HLI	rs151344482
Exac	rs151344482
Gnomad	rs151344482
Varsome	rs151344482
LitVar	rs151344482
Map	rs151344482
PheGenI	rs151344482
Biobank	rs151344482
1000 genomes	rs151344482
hgdp	rs151344482
ensembl	rs151344482
geneview	rs151344482
scholar	rs151344482
google	rs151344482
pharmgkb	rs151344482
gwascentral	rs151344482
openSNP	rs151344482
23andMe	rs151344482
SNPshot	rs151344482
SNPdbe	rs151344482
MSV3d	rs151344482
GWAS Ctlg	rs151344482

Max Magnitude

0

ClinVar
Risk	rs151344482(G;G)
Alt	rs151344482(G;G)
Reference	Rs151344482(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CYBB
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.37655346A>G
CLNSRC	UniProtKB (protein) UniProtKB (variants)
CLNACC	RCV000059266.1,