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rs398122867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122867(-;-)
Make rs398122867(-;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position56952109
GeneC8B
is asnp
is mentioned by
dbSNPrs398122867
ebirs398122867
HLIrs398122867
Exacrs398122867
Varsomers398122867
Maprs398122867
PheGenIrs398122867
hapmaprs398122867
1000 genomesrs398122867
hgdprs398122867
ensemblrs398122867
gopubmedrs398122867
geneviewrs398122867
scholarrs398122867
googlers398122867
pharmgkbrs398122867
gwascentralrs398122867
openSNPrs398122867
23andMers398122867
23andMe allrs398122867
SNP Nexus

SNPshotrs398122867
SNPdbers398122867
MSV3drs398122867
GWAS Ctlgrs398122867
Max Magnitude0
ClinVar
Risk rs398122867(;)
Alt rs398122867(;)
Reference rs398122867(C;C)
Significance Pathogenic
Disease Complement component 8 deficiency type 2
Variation info
Gene C8B
CLNDBN Complement component 8 deficiency type 2
Reversed 1
HGVS NC_000001.10:g.57417782delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000029241.29,