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rs121964917

From SNPedia

Orientationminus
Stabilizedminus
Make rs121964917(C;C)
Make rs121964917(C;T)
Make rs121964917(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109749594
GeneCFI
is asnp
is mentioned by
dbSNPrs121964917
ebirs121964917
HLIrs121964917
Exacrs121964917
Varsomers121964917
Maprs121964917
PheGenIrs121964917
hapmaprs121964917
1000 genomesrs121964917
hgdprs121964917
ensemblrs121964917
gopubmedrs121964917
geneviewrs121964917
scholarrs121964917
googlers121964917
pharmgkbrs121964917
gwascentralrs121964917
openSNPrs121964917
23andMers121964917
23andMe allrs121964917
SNP Nexus

SNPshotrs121964917
SNPdbers121964917
MSV3drs121964917
GWAS Ctlgrs121964917
Max Magnitude
OMIM217030
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121964917(T;T)
Alt rs121964917(T;T)
Reference rs121964917(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 3
Variation info
Gene CFI
CLNDBN Atypical hemolytic-uremic syndrome 3
Reversed 1
HGVS NC_000004.11:g.110670750G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012908.2,