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rs796065030

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796065030(-;-)
Make rs796065030(-;GA)
Make rs796065030(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position183574587
GeneNCF2
is asnp
is mentioned by
dbSNPrs796065030
ebirs796065030
HLIrs796065030
Exacrs796065030
Varsomers796065030
Maprs796065030
PheGenIrs796065030
hapmaprs796065030
1000 genomesrs796065030
hgdprs796065030
ensemblrs796065030
gopubmedrs796065030
geneviewrs796065030
scholarrs796065030
googlers796065030
pharmgkbrs796065030
gwascentralrs796065030
openSNPrs796065030
23andMers796065030
23andMe allrs796065030
SNP Nexus

SNPshotrs796065030
SNPdbers796065030
MSV3drs796065030
GWAS Ctlgrs796065030
Max Magnitude0
ClinVar
Risk rs796065030(GA;GA)
Alt rs796065030(GA;GA)
Reference rs796065030(;)
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.183543723_183543724dupTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000002327.3,