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

rs398123065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123065(C;T)
Make rs398123065(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position31947950
GeneCFB
is asnp
is mentioned by
dbSNPrs398123065
ebirs398123065
HLIrs398123065
Exacrs398123065
Varsomers398123065
Maprs398123065
PheGenIrs398123065
hapmaprs398123065
1000 genomesrs398123065
hgdprs398123065
ensemblrs398123065
gopubmedrs398123065
geneviewrs398123065
scholarrs398123065
googlers398123065
pharmgkbrs398123065
gwascentralrs398123065
openSNPrs398123065
23andMers398123065
23andMe allrs398123065
SNP Nexus

SNPshotrs398123065
SNPdbers398123065
MSV3drs398123065
GWAS Ctlgrs398123065
Max Magnitude0
ClinVar
Risk rs398123065(T;T)
Alt rs398123065(T;T)
Reference rs398123065(C;C)
Significance Pathogenic
Disease Complement factor B deficiency
Variation info
Gene CFB
CLNDBN Complement factor B deficiency
Reversed 0
HGVS NC_000006.11:g.31915727C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000077869.3,