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rs121913051

From SNPedia

Orientationplus
Stabilizedplus
Make rs121913051(C;C)
Make rs121913051(C;G)
Make rs121913051(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196747260
GeneCFH
is asnp
is mentioned by
dbSNPrs121913051
dbSNP (old)rs121913051
ClinGenrs121913051
ebirs121913051
HLIrs121913051
Exacrs121913051
Gnomadrs121913051
Varsomers121913051
Maprs121913051
PheGenIrs121913051
Biobankrs121913051
1000 genomesrs121913051
hgdprs121913051
ensemblrs121913051
gopubmedrs121913051
geneviewrs121913051
scholarrs121913051
googlers121913051
pharmgkbrs121913051
gwascentralrs121913051
openSNPrs121913051
23andMers121913051
23andMe allrs121913051
SNP Nexus

SNPshotrs121913051
SNPdbers121913051
MSV3drs121913051
GWAS Ctlgrs121913051
Max Magnitude
OMIM134370
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913051(G;G) rs121913051(T;T)
Alt rs121913051(G;G) rs121913051(T;T)
Reference rs121913051(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 1 CFH-Related Disorders
Variation info
Gene CFH
CLNDBN Atypical hemolytic-uremic syndrome 1 CFH-Related Disorders
Reversed 0
HGVS NC_000001.10:g.196716390C>G; NC_000001.10:g.196716390C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018008.2, RCV000276556.1,