{{Rsnum
|rsid=121912491
|Chromosome=3
|position=49131128
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LAMB2
|Gene_s=LAMB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=150325
|rsnum=121912491
|variant=0006
}}{{ClinVar
|rsid=121912491
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=49168561
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LAMB2:3913
|GENE_NAME=LAMB2
|GENE_ID=3913
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.49168561C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=150325.0006
|CLNSIG=5
|CLNCUI=CN078918
|CLNDBN=Nephrotic syndrome, type 5, with or without ocular abnormalities
|Disease=Nephrotic syndrome
|CLNACC=RCV000015633.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280113:614199:306507
}}