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rs876657370

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657370(-;-)
Make rs876657370(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position94262525
GenePLCE1
is asnp
is mentioned by
dbSNPrs876657370
ebirs876657370
HLIrs876657370
Exacrs876657370
Varsomers876657370
Maprs876657370
PheGenIrs876657370
hapmaprs876657370
1000 genomesrs876657370
hgdprs876657370
ensemblrs876657370
gopubmedrs876657370
geneviewrs876657370
scholarrs876657370
googlers876657370
pharmgkbrs876657370
gwascentralrs876657370
openSNPrs876657370
23andMers876657370
23andMe allrs876657370
SNP Nexus

SNPshotrs876657370
SNPdbers876657370
MSV3drs876657370
GWAS Ctlgrs876657370
Max Magnitude0
ClinVar
Risk rs876657370(;)
Alt rs876657370(;)
Reference rs876657370(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene PLCE1
CLNDBN Nephrotic syndrome, type 3
Reversed 0
HGVS NC_000010.10:g.96022282delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002438.3,