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rs796065033

From SNPedia

Orientationminus
Geno Mag Summary
(AAGAAGGAC;AAGAAGGAC) 0 common in clinvar
Make rs796065033(-;-)
Make rs796065033(-;AAGAAGGAC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position183590267
GeneNCF2
is asnp
is mentioned by
dbSNPrs796065033
ebirs796065033
HLIrs796065033
Exacrs796065033
Varsomers796065033
Maprs796065033
PheGenIrs796065033
hapmaprs796065033
1000 genomesrs796065033
hgdprs796065033
ensemblrs796065033
gopubmedrs796065033
geneviewrs796065033
scholarrs796065033
googlers796065033
pharmgkbrs796065033
gwascentralrs796065033
openSNPrs796065033
23andMers796065033
23andMe allrs796065033
SNP Nexus

SNPshotrs796065033
SNPdbers796065033
MSV3drs796065033
GWAS Ctlgrs796065033
Max Magnitude0
ClinVar
Risk rs796065033(;)
Alt rs796065033(;)
Reference rs796065033(AAGAAGGAC;AAGAAGGAC)
Significance Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene NCF2
CLNDBN Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
Reversed 1
HGVS NC_000001.10:g.183559402_183559410delGTCCTTCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002333.3,