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rs267606721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606721(C;C)
Make rs267606721(C;T)
ReferenceGRCh37.p10 37.5/138
Chromosome19
Position863116
GeneCFD
is asnp
is mentioned by
dbSNPrs267606721
ebirs267606721
HLIrs267606721
Exacrs267606721
Varsomers267606721
Maprs267606721
PheGenIrs267606721
hapmaprs267606721
1000 genomesrs267606721
hgdprs267606721
ensemblrs267606721
gopubmedrs267606721
geneviewrs267606721
scholarrs267606721
googlers267606721
pharmgkbrs267606721
gwascentralrs267606721
openSNPrs267606721
23andMers267606721
23andMe allrs267606721
SNP Nexus

SNPshotrs267606721
SNPdbers267606721
MSV3drs267606721
GWAS Ctlgrs267606721
Max Magnitude0
ClinVar
Risk rs267606721(C;C)
Alt rs267606721(C;C)
Reference rs267606721(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.863116T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018033.27,