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rs121909748

From SNPedia

Orientationplus
Stabilizedplus
Make rs121909748(A;A)
Make rs121909748(A;G)
Make rs121909748(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31948443
GeneCFB
is asnp
is mentioned by
dbSNPrs121909748
dbSNP (old)rs121909748
ClinGenrs121909748
ebirs121909748
HLIrs121909748
Exacrs121909748
Varsomers121909748
Maprs121909748
PheGenIrs121909748
Biobankrs121909748
1000 genomesrs121909748
hgdprs121909748
ensemblrs121909748
gopubmedrs121909748
geneviewrs121909748
scholarrs121909748
googlers121909748
pharmgkbrs121909748
gwascentralrs121909748
openSNPrs121909748
23andMers121909748
23andMe allrs121909748
SNP Nexus

SNPshotrs121909748
SNPdbers121909748
MSV3drs121909748
GWAS Ctlgrs121909748
Max Magnitude
OMIM138470
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909748(G;G)
Alt rs121909748(G;G)
Reference rs121909748(A;A)
Significance Other
Disease Atypical hemolytic-uremic syndrome 4
Variation info
Gene CFB
CLNDBN Atypical hemolytic-uremic syndrome 4
Reversed 0
HGVS NC_000006.11:g.31916220A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017460.3,