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rs876657377

From SNPedia

Orientationplus
Geno Mag Summary
(AAGGAGGATC;AAGGAGGATC) 0 common in clinvar
Make rs876657377(-;-)
Make rs876657377(-;AAGGAGGATC)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position36864944
GeneNCF4
is asnp
is mentioned by
dbSNPrs876657377
ebirs876657377
HLIrs876657377
Exacrs876657377
Varsomers876657377
Maprs876657377
PheGenIrs876657377
hapmaprs876657377
1000 genomesrs876657377
hgdprs876657377
ensemblrs876657377
gopubmedrs876657377
geneviewrs876657377
scholarrs876657377
googlers876657377
pharmgkbrs876657377
gwascentralrs876657377
openSNPrs876657377
23andMers876657377
23andMe allrs876657377
SNP Nexus

SNPshotrs876657377
SNPdbers876657377
MSV3drs876657377
GWAS Ctlgrs876657377
Max Magnitude0
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,