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rs267606720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606720(G;G)
Make rs267606720(G;T)
ReferenceGRCh37.p10 37.5/138
Chromosome19
Position863114
GeneCFD
is asnp
is mentioned by
dbSNPrs267606720
ebirs267606720
HLIrs267606720
Exacrs267606720
Varsomers267606720
Maprs267606720
PheGenIrs267606720
hapmaprs267606720
1000 genomesrs267606720
hgdprs267606720
ensemblrs267606720
gopubmedrs267606720
geneviewrs267606720
scholarrs267606720
googlers267606720
pharmgkbrs267606720
gwascentralrs267606720
openSNPrs267606720
23andMers267606720
23andMe allrs267606720
SNP Nexus

SNPshotrs267606720
SNPdbers267606720
MSV3drs267606720
GWAS Ctlgrs267606720
Max Magnitude0
ClinVar
Risk rs267606720(G;G)
Alt rs267606720(G;G)
Reference rs267606720(T;T)
Significance Pathogenic
Disease Complement factor d deficiency
Variation info
Gene CFD
CLNDBN Complement factor d deficiency
Reversed 0
HGVS NC_000019.9:g.863114T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018033.27,