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rs121909585

From SNPedia

Orientationminus
Stabilizedminus
Make rs121909585(A;A)
Make rs121909585(A;G)
Make rs121909585(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position6692971
GeneC3
is asnp
is mentioned by
dbSNPrs121909585
dbSNP (old)rs121909585
ClinGenrs121909585
ebirs121909585
HLIrs121909585
Exacrs121909585
Gnomadrs121909585
Varsomers121909585
Maprs121909585
PheGenIrs121909585
Biobankrs121909585
1000 genomesrs121909585
hgdprs121909585
ensemblrs121909585
gopubmedrs121909585
geneviewrs121909585
scholarrs121909585
googlers121909585
pharmgkbrs121909585
gwascentralrs121909585
openSNPrs121909585
23andMers121909585
23andMe allrs121909585
SNP Nexus

SNPshotrs121909585
SNPdbers121909585
MSV3drs121909585
GWAS Ctlgrs121909585
Max Magnitude
OMIM120700
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909585(A;A)
Alt rs121909585(A;A)
Reference rs121909585(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.6692982C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000018591.3,