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rs267606710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606710(C;T)
Make rs267606710(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position47612492
GeneCD2AP
is asnp
is mentioned by
dbSNPrs267606710
ebirs267606710
HLIrs267606710
Exacrs267606710
Varsomers267606710
Maprs267606710
PheGenIrs267606710
hapmaprs267606710
1000 genomesrs267606710
hgdprs267606710
ensemblrs267606710
gopubmedrs267606710
geneviewrs267606710
scholarrs267606710
googlers267606710
pharmgkbrs267606710
gwascentralrs267606710
openSNPrs267606710
23andMers267606710
23andMe allrs267606710
SNP Nexus

SNPshotrs267606710
SNPdbers267606710
MSV3drs267606710
GWAS Ctlgrs267606710
Max Magnitude0
ClinVar
Risk rs267606710(A,T;A,T)
Alt rs267606710(A,T;A,T)
Reference rs267606710(C;C)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 3
Variation info
Gene CD2AP
CLNDBN Focal segmental glomerulosclerosis 3
Reversed 0
HGVS NC_000006.11:g.47580228C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006058.2,