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rs121913057

From SNPedia

Orientationplus
Stabilizedplus
Make rs121913057(A;A)
Make rs121913057(A;T)
Make rs121913057(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196737575
GeneCFH
is asnp
is mentioned by
dbSNPrs121913057
dbSNP (old)rs121913057
ClinGenrs121913057
ebirs121913057
HLIrs121913057
Exacrs121913057
Gnomadrs121913057
Varsomers121913057
Maprs121913057
PheGenIrs121913057
Biobankrs121913057
1000 genomesrs121913057
hgdprs121913057
ensemblrs121913057
gopubmedrs121913057
geneviewrs121913057
scholarrs121913057
googlers121913057
pharmgkbrs121913057
gwascentralrs121913057
openSNPrs121913057
23andMers121913057
23andMe allrs121913057
SNP Nexus

SNPshotrs121913057
SNPdbers121913057
MSV3drs121913057
GWAS Ctlgrs121913057
Max Magnitude
OMIM134370
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121913057(A;A) rs121913057(C;C)
Alt rs121913057(A;A) rs121913057(C;C)
Reference rs121913057(T;T)
Significance Other
Disease Atypical hemolytic-uremic syndrome 1
Variation info
Gene CFH
CLNDBN Atypical hemolytic-uremic syndrome 1
Reversed 0
HGVS NC_000001.10:g.196706705T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018020.4,