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rs121913063

From SNPedia

Orientationplus
Stabilizedplus
Make rs121913063(G;G)
Make rs121913063(G;T)
Make rs121913063(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196747209
GeneCFH
is asnp
is mentioned by
dbSNPrs121913063
dbSNP (old)rs121913063
ClinGenrs121913063
ebirs121913063
HLIrs121913063
Exacrs121913063
Gnomadrs121913063
Varsomers121913063
Maprs121913063
PheGenIrs121913063
Biobankrs121913063
1000 genomesrs121913063
hgdprs121913063
ensemblrs121913063
gopubmedrs121913063
geneviewrs121913063
scholarrs121913063
googlers121913063
pharmgkbrs121913063
gwascentralrs121913063
openSNPrs121913063
23andMers121913063
23andMe allrs121913063
SNP Nexus

SNPshotrs121913063
SNPdbers121913063
MSV3drs121913063
GWAS Ctlgrs121913063
Max Magnitude
OMIM134370
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121913063(T;T)
Alt rs121913063(T;T)
Reference rs121913063(G;G)
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.196716339G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018031.5,