Have questions? Visit https://www.reddit.com/r/SNPedia

rs374402066

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374402066(A;A)
Make rs374402066(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position183577661
GeneNCF2
is asnp
is mentioned by
dbSNPrs374402066
ebirs374402066
HLIrs374402066
Exacrs374402066
Varsomers374402066
Maprs374402066
PheGenIrs374402066
hapmaprs374402066
1000 genomesrs374402066
hgdprs374402066
ensemblrs374402066
gopubmedrs374402066
geneviewrs374402066
scholarrs374402066
googlers374402066
pharmgkbrs374402066
gwascentralrs374402066
openSNPrs374402066
23andMers374402066
23andMe allrs374402066
SNP Nexus

SNPshotrs374402066
SNPdbers374402066
MSV3drs374402066
GWAS Ctlgrs374402066
Max Magnitude0
ClinVar
Risk rs374402066(A;A)
Alt rs374402066(A;A)
Reference rs374402066(G;G)
Significance Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene NCF2
CLNDBN Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
Reversed 0
HGVS NC_000001.10:g.183546796G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002329.3,