Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912491(A;A)
Make rs121912491(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position49131128
GeneLAMB2
is asnp
is mentioned by
dbSNPrs121912491
ebirs121912491
HLIrs121912491
Exacrs121912491
Varsomers121912491
Maprs121912491
PheGenIrs121912491
hapmaprs121912491
1000 genomesrs121912491
hgdprs121912491
ensemblrs121912491
gopubmedrs121912491
geneviewrs121912491
scholarrs121912491
googlers121912491
pharmgkbrs121912491
gwascentralrs121912491
openSNPrs121912491
23andMers121912491
23andMe allrs121912491
SNP Nexus

SNPshotrs121912491
SNPdbers121912491
MSV3drs121912491
GWAS Ctlgrs121912491
Max Magnitude0
OMIM150325
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121912491(A;A)
Alt rs121912491(A;A)
Reference rs121912491(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene LAMB2
CLNDBN Nephrotic syndrome, type 5, with or without ocular abnormalities
Reversed 1
HGVS NC_000003.11:g.49168561C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015633.25,