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rs794729228

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729228(C;T)
Make rs794729228(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position6714208
GeneC3
is asnp
is mentioned by
dbSNPrs794729228
ebirs794729228
HLIrs794729228
Exacrs794729228
Varsomers794729228
Maprs794729228
PheGenIrs794729228
hapmaprs794729228
1000 genomesrs794729228
hgdprs794729228
ensemblrs794729228
gopubmedrs794729228
geneviewrs794729228
scholarrs794729228
googlers794729228
pharmgkbrs794729228
gwascentralrs794729228
openSNPrs794729228
23andMers794729228
23andMe allrs794729228
SNP Nexus

SNPshotrs794729228
SNPdbers794729228
MSV3drs794729228
GWAS Ctlgrs794729228
Max Magnitude0
ClinVar
Risk rs794729228(T;T)
Alt rs794729228(T;T)
Reference rs794729228(C;C)
Significance Probable-Pathogenic
Disease Atypical hemolytic-uremic syndrome 5
Variation info
Gene C3
CLNDBN Atypical hemolytic-uremic syndrome 5
Reversed 1
HGVS NC_000019.9:g.6714219G>A
CLNSRC
CLNACC RCV000184049.1,