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rs121964914

From SNPedia

Orientationminus
Stabilizedminus
Make rs121964914(A;A)
Make rs121964914(A;T)
Make rs121964914(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109741074
GeneCFI
is asnp
is mentioned by
dbSNPrs121964914
ebirs121964914
HLIrs121964914
Exacrs121964914
Varsomers121964914
Maprs121964914
PheGenIrs121964914
hapmaprs121964914
1000 genomesrs121964914
hgdprs121964914
ensemblrs121964914
gopubmedrs121964914
geneviewrs121964914
scholarrs121964914
googlers121964914
pharmgkbrs121964914
gwascentralrs121964914
openSNPrs121964914
23andMers121964914
23andMe allrs121964914
SNP Nexus

SNPshotrs121964914
SNPdbers121964914
MSV3drs121964914
GWAS Ctlgrs121964914
Max Magnitude
OMIM217030
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121964914(T;T)
Alt rs121964914(T;T)
Reference rs121964914(A;A)
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.110662230T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012905.2,