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rs121964915

From SNPedia

Orientationminus
Stabilizedminus
Make rs121964915(A;A)
Make rs121964915(A;G)
Make rs121964915(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109741008
GeneCFI
is asnp
is mentioned by
dbSNPrs121964915
ebirs121964915
HLIrs121964915
Exacrs121964915
Varsomers121964915
Maprs121964915
PheGenIrs121964915
hapmaprs121964915
1000 genomesrs121964915
hgdprs121964915
ensemblrs121964915
gopubmedrs121964915
geneviewrs121964915
scholarrs121964915
googlers121964915
pharmgkbrs121964915
gwascentralrs121964915
openSNPrs121964915
23andMers121964915
23andMe allrs121964915
SNP Nexus

SNPshotrs121964915
SNPdbers121964915
MSV3drs121964915
GWAS Ctlgrs121964915
Max Magnitude
OMIM217030
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121964915(A;A)
Alt rs121964915(A;A)
Reference rs121964915(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.110662164C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012906.2,