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rs121913055

From SNPedia

Orientationplus
Stabilizedplus
Make rs121913055(G;G)
Make rs121913055(G;T)
Make rs121913055(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196747183
GeneCFH
is asnp
is mentioned by
dbSNPrs121913055
dbSNP (old)rs121913055
ClinGenrs121913055
ebirs121913055
HLIrs121913055
Exacrs121913055
Varsomers121913055
Maprs121913055
PheGenIrs121913055
Biobankrs121913055
1000 genomesrs121913055
hgdprs121913055
ensemblrs121913055
gopubmedrs121913055
geneviewrs121913055
scholarrs121913055
googlers121913055
pharmgkbrs121913055
gwascentralrs121913055
openSNPrs121913055
23andMers121913055
23andMe allrs121913055
SNP Nexus

SNPshotrs121913055
SNPdbers121913055
MSV3drs121913055
GWAS Ctlgrs121913055
Max Magnitude
OMIM134370
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913055(G;G)
Alt rs121913055(G;G)
Reference rs121913055(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.196716313T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018014.3,