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rs755796920

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755796920(G;T)
Make rs755796920(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position183573229
GeneNCF2
is asnp
is mentioned by
dbSNPrs755796920
ebirs755796920
HLIrs755796920
Exacrs755796920
Varsomers755796920
Maprs755796920
PheGenIrs755796920
hapmaprs755796920
1000 genomesrs755796920
hgdprs755796920
ensemblrs755796920
gopubmedrs755796920
geneviewrs755796920
scholarrs755796920
googlers755796920
pharmgkbrs755796920
gwascentralrs755796920
openSNPrs755796920
23andMers755796920
23andMe allrs755796920
SNP Nexus

SNPshotrs755796920
SNPdbers755796920
MSV3drs755796920
GWAS Ctlgrs755796920
Max Magnitude0
ClinVar
Risk rs755796920(A,T;A,T)
Alt rs755796920(A,T;A,T)
Reference rs755796920(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.183542364G>A
CLNSRC
CLNACC RCV000178769.1,