{{Rsnum
|rsid=137852665
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=IGHMBP2
|position=68934466
|Gene_s=IGHMBP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600502
|variant=0001
|rsnum=137852665
}}{{ClinVar
|rsid=137852665
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=68701934
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=IGHMBP2:3508
|GENE_NAME=IGHMBP2
|GENE_ID=3508
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68701934G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600502.0001
|CLNSIG=5
|CLNCUI=C0043116
|CLNDBN=Werdnig-Hoffmann disease
|Disease=Werdnig-Hoffmann disease
|CLNACC=RCV000009682.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1352:C0043116:253300:604320:70:83330:64383006
}}