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rs121909584

From SNPedia

Orientationminus
Stabilizedminus
Make rs121909584(C;C)
Make rs121909584(C;T)
Make rs121909584(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position6693033
GeneC3
is asnp
is mentioned by
dbSNPrs121909584
dbSNP (old)rs121909584
ClinGenrs121909584
ebirs121909584
HLIrs121909584
Exacrs121909584
Gnomadrs121909584
Varsomers121909584
Maprs121909584
PheGenIrs121909584
Biobankrs121909584
1000 genomesrs121909584
hgdprs121909584
ensemblrs121909584
gopubmedrs121909584
geneviewrs121909584
scholarrs121909584
googlers121909584
pharmgkbrs121909584
gwascentralrs121909584
openSNPrs121909584
23andMers121909584
23andMe allrs121909584
SNP Nexus

SNPshotrs121909584
SNPdbers121909584
MSV3drs121909584
GWAS Ctlgrs121909584
Max Magnitude
OMIM120700
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909584(T;T)
Alt rs121909584(T;T)
Reference rs121909584(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 5
Variation info
Gene C3
CLNDBN Atypical hemolytic-uremic syndrome 5
Reversed 1
HGVS NC_000019.9:g.6693044G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000018590.3,