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rs121964913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs121964913(C;T)
Make rs121964913(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109746231
GeneCFI
is asnp
is mentioned by
dbSNPrs121964913
ebirs121964913
HLIrs121964913
Exacrs121964913
Varsomers121964913
Maprs121964913
PheGenIrs121964913
hapmaprs121964913
1000 genomesrs121964913
hgdprs121964913
ensemblrs121964913
gopubmedrs121964913
geneviewrs121964913
scholarrs121964913
googlers121964913
pharmgkbrs121964913
gwascentralrs121964913
openSNPrs121964913
23andMers121964913
23andMe allrs121964913
SNP Nexus

SNPshotrs121964913
SNPdbers121964913
MSV3drs121964913
GWAS Ctlgrs121964913
Max Magnitude0
OMIM217030
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121964913(T;T)
Alt rs121964913(T;T)
Reference rs121964913(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.110667387G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012904.2,