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rs267606955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606955(C;T)
Make rs267606955(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position94259072
GenePLCE1
is asnp
is mentioned by
dbSNPrs267606955
ebirs267606955
HLIrs267606955
Exacrs267606955
Varsomers267606955
Maprs267606955
PheGenIrs267606955
hapmaprs267606955
1000 genomesrs267606955
hgdprs267606955
ensemblrs267606955
gopubmedrs267606955
geneviewrs267606955
scholarrs267606955
googlers267606955
pharmgkbrs267606955
gwascentralrs267606955
openSNPrs267606955
23andMers267606955
23andMe allrs267606955
SNP Nexus

SNPshotrs267606955
SNPdbers267606955
MSV3drs267606955
GWAS Ctlgrs267606955
Max Magnitude0
ClinVar
Risk rs267606955(A,T;A,T)
Alt rs267606955(A,T;A,T)
Reference rs267606955(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene PLCE1
CLNDBN Nephrotic syndrome, type 3
Reversed 0
HGVS NC_000010.10:g.96018829C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002444.3,