rs387906485

Orientation

plus

Stabilized

plus

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

Make rs387906485(A;A)

Make rs387906485(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

37783600

Gene

CYBB

is a	snp
is	mentioned by
dbSNP	rs387906485
dbSNP (classic)	rs387906485
ClinGen	rs387906485
ebi	rs387906485
HLI	rs387906485
Exac	rs387906485
Gnomad	rs387906485
Varsome	rs387906485
LitVar	rs387906485
Map	rs387906485
PheGenI	rs387906485
Biobank	rs387906485
1000 genomes	rs387906485
hgdp	rs387906485
ensembl	rs387906485
geneview	rs387906485
scholar	rs387906485
google	rs387906485
pharmgkb	rs387906485
gwascentral	rs387906485
openSNP	rs387906485
23andMe	rs387906485
SNPshot	rs387906485
SNPdbe	rs387906485
MSV3d	rs387906485
GWAS Ctlg	rs387906485

Max Magnitude

0

ClinVar
Risk	rs387906485(A;A) rs387906485(T;T)
Alt	rs387906485(A;A) rs387906485(T;T)
Reference	Rs387906485(G;G)
Significance	Pathogenic
Disease	Chronic granulomatous disease not provided
Variation	info
Gene	CYBB
CLNDBN	Chronic granulomatous disease, X-linked not provided
Reversed	0
HGVS	NC_000023.10:g.37642853G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011680.5, RCV000482302.1,