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rs121913060

From SNPedia

Orientationplus
Stabilizedplus
Make rs121913060(G;G)
Make rs121913060(G;T)
Make rs121913060(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196747131
GeneCFH
is asnp
is mentioned by
dbSNPrs121913060
dbSNP (old)rs121913060
ClinGenrs121913060
ebirs121913060
HLIrs121913060
Exacrs121913060
Varsomers121913060
Maprs121913060
PheGenIrs121913060
Biobankrs121913060
1000 genomesrs121913060
hgdprs121913060
ensemblrs121913060
gopubmedrs121913060
geneviewrs121913060
scholarrs121913060
googlers121913060
pharmgkbrs121913060
gwascentralrs121913060
openSNPrs121913060
23andMers121913060
23andMe allrs121913060
SNP Nexus

SNPshotrs121913060
SNPdbers121913060
MSV3drs121913060
GWAS Ctlgrs121913060
Max Magnitude
OMIM134370
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121913060(T;T)
Alt rs121913060(T;T)
Reference rs121913060(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.196716261G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018027.4,