{{Rsnum
|rsid=121912488
|Chromosome=3
|position=49131129
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMB2
|Gene_s=LAMB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=150325
|rsnum=121912488
|variant=0002
}}{{ClinVar
|rsid=121912488
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=49168562
|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.49168562G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=150325.0002
|CLNSIG=5
|CLNCUI=C1836876
|CLNDBN=Pierson syndrome
|Disease=Pierson syndrome
|CLNACC=RCV000015629.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836876:609049:2670
}}