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rs121909586

From SNPedia

Orientationminus
Stabilizedminus
Make rs121909586(C;C)
Make rs121909586(C;G)
Make rs121909586(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position6697673
GeneC3
is asnp
is mentioned by
dbSNPrs121909586
dbSNP (old)rs121909586
ClinGenrs121909586
ebirs121909586
HLIrs121909586
Exacrs121909586
Gnomadrs121909586
Varsomers121909586
Maprs121909586
PheGenIrs121909586
Biobankrs121909586
1000 genomesrs121909586
hgdprs121909586
ensemblrs121909586
gopubmedrs121909586
geneviewrs121909586
scholarrs121909586
googlers121909586
pharmgkbrs121909586
gwascentralrs121909586
openSNPrs121909586
23andMers121909586
23andMe allrs121909586
SNP Nexus

SNPshotrs121909586
SNPdbers121909586
MSV3drs121909586
GWAS Ctlgrs121909586
Max Magnitude
OMIM120700
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909586(G;G) rs121909586(T;T)
Alt rs121909586(G;G) rs121909586(T;T)
Reference rs121909586(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.6697684G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018592.3,