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rs876657369

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657369(-;-)
Make rs876657369(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position94032192
GenePLCE1
is asnp
is mentioned by
dbSNPrs876657369
ebirs876657369
HLIrs876657369
Exacrs876657369
Varsomers876657369
Maprs876657369
PheGenIrs876657369
hapmaprs876657369
1000 genomesrs876657369
hgdprs876657369
ensemblrs876657369
gopubmedrs876657369
geneviewrs876657369
scholarrs876657369
googlers876657369
pharmgkbrs876657369
gwascentralrs876657369
openSNPrs876657369
23andMers876657369
23andMe allrs876657369
SNP Nexus

SNPshotrs876657369
SNPdbers876657369
MSV3drs876657369
GWAS Ctlgrs876657369
Max Magnitude0
ClinVar
Risk rs876657369(;)
Alt rs876657369(;)
Reference rs876657369(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene PLCE1
CLNDBN Nephrotic syndrome, type 3
Reversed 0
HGVS NC_000010.10:g.95791949delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002435.3,