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rs121909583

From SNPedia

Orientationminus
Stabilizedminus
Make rs121909583(A;A)
Make rs121909583(A;G)
Make rs121909583(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position6709754
GeneC3
is asnp
is mentioned by
dbSNPrs121909583
dbSNP (old)rs121909583
ClinGenrs121909583
ebirs121909583
HLIrs121909583
Exacrs121909583
Gnomadrs121909583
Varsomers121909583
Maprs121909583
PheGenIrs121909583
Biobankrs121909583
1000 genomesrs121909583
hgdprs121909583
ensemblrs121909583
gopubmedrs121909583
geneviewrs121909583
scholarrs121909583
googlers121909583
pharmgkbrs121909583
gwascentralrs121909583
openSNPrs121909583
23andMers121909583
23andMe allrs121909583
SNP Nexus

SNPshotrs121909583
SNPdbers121909583
MSV3drs121909583
GWAS Ctlgrs121909583
Max Magnitude
OMIM120700
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909583(A;A)
Alt rs121909583(A;A)
Reference rs121909583(G;G)
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.6709765C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000018589.2,