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rs886039869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs886039869(C;C)
Make rs886039869(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position196740786
GeneCFH
is asnp
is mentioned by
dbSNPrs886039869
dbSNP (old)rs886039869
ClinGenrs886039869
ebirs886039869
HLIrs886039869
Exacrs886039869
Gnomadrs886039869
Varsomers886039869
Maprs886039869
PheGenIrs886039869
Biobankrs886039869
1000 genomesrs886039869
hgdprs886039869
ensemblrs886039869
gopubmedrs886039869
geneviewrs886039869
scholarrs886039869
googlers886039869
pharmgkbrs886039869
gwascentralrs886039869
openSNPrs886039869
23andMers886039869
23andMe allrs886039869
SNPshotrs886039869
SNPdbers886039869
MSV3drs886039869
GWAS Ctlgrs886039869
Max Magnitude0
ClinVar
Risk rs886039869(C;C)
Alt rs886039869(C;C)
Reference Rs886039869(T;T)
Significance Probable-Pathogenic
Disease Atypical hemolytic-uremic syndrome 1
Variation info
Gene CFH
CLNDBN Atypical hemolytic-uremic syndrome 1
Reversed 0
HGVS NC_000001.10:g.196709916T>C
CLNSRC
CLNACC RCV000256395.1,