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rs121964918

From SNPedia

Orientationminus
Stabilizedminus
Make rs121964918(A;A)
Make rs121964918(A;G)
Make rs121964918(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109741090
GeneCFI
is asnp
is mentioned by
dbSNPrs121964918
ebirs121964918
HLIrs121964918
Exacrs121964918
Varsomers121964918
Maprs121964918
PheGenIrs121964918
hapmaprs121964918
1000 genomesrs121964918
hgdprs121964918
ensemblrs121964918
gopubmedrs121964918
geneviewrs121964918
scholarrs121964918
googlers121964918
pharmgkbrs121964918
gwascentralrs121964918
openSNPrs121964918
23andMers121964918
23andMe allrs121964918
SNP Nexus

SNPshotrs121964918
SNPdbers121964918
MSV3drs121964918
GWAS Ctlgrs121964918
Max Magnitude
OMIM217030
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121964918(A;A)
Alt rs121964918(A;A)
Reference rs121964918(G;G)
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.110662246C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012909.2,