{{Rsnum
|rsid=398122418
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MAGEL2
|position=23644619
|Gene_s=MAGEL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000074487.3
|CLNALLE=1
|CLNDBN=Prader-Willi-like syndrome
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN182242:615547
|CLNHGVS=NC_000015.9:g.23889766G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605283.0004
|Disease=Prader-Willi-like syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=MAGEL2:54551
|GENE_ID=54551
|GENE_NAME=MAGEL2
|REF=G
|RSPOS=23889766
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122418
}}