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rs121909590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs121909590(C;T)
Make rs121909590(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position207757091
GeneCD46
is asnp
is mentioned by
dbSNPrs121909590
dbSNP (classic)rs121909590
ClinGenrs121909590
ebirs121909590
HLIrs121909590
Exacrs121909590
Gnomadrs121909590
Varsomers121909590
LitVarrs121909590
Maprs121909590
PheGenIrs121909590
Biobankrs121909590
1000 genomesrs121909590
hgdprs121909590
ensemblrs121909590
geneviewrs121909590
scholarrs121909590
googlers121909590
pharmgkbrs121909590
gwascentralrs121909590
openSNPrs121909590
23andMers121909590
SNPshotrs121909590
SNPdbers121909590
MSV3drs121909590
GWAS Ctlgrs121909590
Max Magnitude0
OMIM120920
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909590(T;T)
Alt rs121909590(T;T)
Reference Rs121909590(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 2
Variation info
Gene CD46
CLNDBN Atypical hemolytic-uremic syndrome 2
Reversed 0
HGVS NC_000001.10:g.207930436C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018576.2,