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rs398122811

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122811(-;-)
Make rs398122811(-;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position41201621
GeneC6
is asnp
is mentioned by
dbSNPrs398122811
ebirs398122811
HLIrs398122811
Exacrs398122811
Varsomers398122811
Maprs398122811
PheGenIrs398122811
hapmaprs398122811
1000 genomesrs398122811
hgdprs398122811
ensemblrs398122811
gopubmedrs398122811
geneviewrs398122811
scholarrs398122811
googlers398122811
pharmgkbrs398122811
gwascentralrs398122811
openSNPrs398122811
23andMers398122811
23andMe allrs398122811
SNP Nexus

SNPshotrs398122811
SNPdbers398122811
MSV3drs398122811
GWAS Ctlgrs398122811
Max Magnitude0
ClinVar
Risk rs398122811(;)
Alt rs398122811(;)
Reference rs398122811(C;C)
Significance Pathogenic
Disease Complement component 6 deficiency
Variation info
Gene C6
CLNDBN Complement component 6 deficiency
Reversed 1
HGVS NC_000005.9:g.41201723delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000022813.16,