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rs267606954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606954(C;T)
Make rs267606954(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position94032007
GenePLCE1
is asnp
is mentioned by
dbSNPrs267606954
ebirs267606954
HLIrs267606954
Exacrs267606954
Varsomers267606954
Maprs267606954
PheGenIrs267606954
hapmaprs267606954
1000 genomesrs267606954
hgdprs267606954
ensemblrs267606954
gopubmedrs267606954
geneviewrs267606954
scholarrs267606954
googlers267606954
pharmgkbrs267606954
gwascentralrs267606954
openSNPrs267606954
23andMers267606954
23andMe allrs267606954
SNP Nexus

SNPshotrs267606954
SNPdbers267606954
MSV3drs267606954
GWAS Ctlgrs267606954
Max Magnitude0
ClinVar
Risk rs267606954(T;T)
Alt rs267606954(T;T)
Reference rs267606954(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene PLCE1
CLNDBN Nephrotic syndrome, type 3
Reversed 0
HGVS NC_000010.10:g.95791764C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002443.3,