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rs267606953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606953(C;T)
Make rs267606953(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position94322006
GenePLCE1
is asnp
is mentioned by
dbSNPrs267606953
ebirs267606953
HLIrs267606953
Exacrs267606953
Varsomers267606953
Maprs267606953
PheGenIrs267606953
hapmaprs267606953
1000 genomesrs267606953
hgdprs267606953
ensemblrs267606953
gopubmedrs267606953
geneviewrs267606953
scholarrs267606953
googlers267606953
pharmgkbrs267606953
gwascentralrs267606953
openSNPrs267606953
23andMers267606953
23andMe allrs267606953
SNP Nexus

SNPshotrs267606953
SNPdbers267606953
MSV3drs267606953
GWAS Ctlgrs267606953
Max Magnitude0
ClinVar
Risk rs267606953(T;T)
Alt rs267606953(T;T)
Reference rs267606953(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene PLCE1
CLNDBN Nephrotic syndrome, type 3
Reversed 0
HGVS NC_000010.10:g.96081763C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002442.3,