rs876657377

Orientation

plus

Stabilized

plus

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

Make rs876657377(-;-)

Make rs876657377(-;AAGGAGGATC)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

36864944

Gene	LOC107985578, NCF4

is a	snp
is	mentioned by
dbSNP	rs876657377
dbSNP (classic)	rs876657377
ClinGen	rs876657377
ebi	rs876657377
HLI	rs876657377
Exac	rs876657377
Gnomad	rs876657377
Varsome	rs876657377
LitVar	rs876657377
Map	rs876657377
PheGenI	rs876657377
Biobank	rs876657377
1000 genomes	rs876657377
hgdp	rs876657377
ensembl	rs876657377
geneview	rs876657377
scholar	rs876657377
google	rs876657377
pharmgkb	rs876657377
gwascentral	rs876657377
openSNP	rs876657377
23andMe	rs876657377
SNPshot	rs876657377
SNPdbe	rs876657377
MSV3d	rs876657377
GWAS Ctlg	rs876657377

Max Magnitude

0

ClinVar
Risk	rs876657377(-;-)
Alt	rs876657377(-;-)
Reference	Rs876657377(AAGGAGGATC;AAGGAGGATC)
Significance	Pathogenic
Disease	Granulomatous disease
Variation	info
Gene	NCF4
CLNDBN	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III
Reversed	0
HGVS	NC_000022.10:g.37260986_37260995delAAGGAGGATC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023112.4,