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rs398124644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
(TTTG;TTTG) 0 common in clinvar
Make rs398124644(-;-)
Make rs398124644(-;TTTG)
ReferenceGRCh38 38.1/141
Chromosome6
Position31951182
GeneCFB
is asnp
is mentioned by
dbSNPrs398124644
ebirs398124644
HLIrs398124644
Exacrs398124644
Varsomers398124644
Maprs398124644
PheGenIrs398124644
hapmaprs398124644
1000 genomesrs398124644
hgdprs398124644
ensemblrs398124644
gopubmedrs398124644
geneviewrs398124644
scholarrs398124644
googlers398124644
pharmgkbrs398124644
gwascentralrs398124644
openSNPrs398124644
23andMers398124644
23andMe allrs398124644
SNP Nexus

SNPshotrs398124644
SNPdbers398124644
MSV3drs398124644
GWAS Ctlgrs398124644
Max Magnitude0
ClinVar
Risk rs398124644(;)
Alt rs398124644(;)
Reference rs398124644(TGTT;TGTT)
Significance Pathogenic
Disease Complement factor B deficiency
Variation info
Gene CFB
CLNDBN Complement factor B deficiency
Reversed 0
HGVS NC_000006.11:g.31918959_31918962delTTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000077870.3,