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rs112534524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112534524(C;T)
Make rs112534524(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109760371
GeneCFI
is asnp
is mentioned by
dbSNPrs112534524
ebirs112534524
HLIrs112534524
Exacrs112534524
Varsomers112534524
Maprs112534524
PheGenIrs112534524
hapmaprs112534524
1000 genomesrs112534524
hgdprs112534524
ensemblrs112534524
gopubmedrs112534524
geneviewrs112534524
scholarrs112534524
googlers112534524
pharmgkbrs112534524
gwascentralrs112534524
openSNPrs112534524
23andMers112534524
23andMe allrs112534524
SNP Nexus

SNPshotrs112534524
SNPdbers112534524
MSV3drs112534524
GWAS Ctlgrs112534524
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs112534524(G,T;G,T)
Alt rs112534524(G,T;G,T)
Reference rs112534524(C;C)
Significance Pathogenic
Disease Atypical hemolytic-uremic syndrome 3
Variation info
Gene CFI
CLNDBN Atypical hemolytic-uremic syndrome 3
Reversed 0
HGVS NC_000004.11:g.110681527C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055784.1,