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rs769399002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769399002(-;-)
Make rs769399002(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49122063
GeneLAMB2, USP19
is asnp
is mentioned by
dbSNPrs769399002
ClinGenrs769399002
ebirs769399002
HLIrs769399002
Exacrs769399002
Varsomers769399002
Maprs769399002
PheGenIrs769399002
hapmaprs769399002
1000 genomesrs769399002
hgdprs769399002
ensemblrs769399002
gopubmedrs769399002
geneviewrs769399002
scholarrs769399002
googlers769399002
pharmgkbrs769399002
gwascentralrs769399002
openSNPrs769399002
23andMers769399002
23andMe allrs769399002
SNP Nexus

SNPshotrs769399002
SNPdbers769399002
MSV3drs769399002
GWAS Ctlgrs769399002
Max Magnitude0
ClinVar
Risk rs769399002(-;-)
Alt rs769399002(-;-)
Reference Rs769399002(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene LAMB2 USP19
CLNDBN Nephrotic syndrome, type 5, with or without ocular abnormalities
Reversed 0
HGVS NC_000003.11:g.49159496delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015637.27,