{{Rsnum
|rsid=397514475
|Chromosome=18
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PIGN
|position=62095902
|Gene_s=PIGN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=18
|CLNACC=RCV000023506.2
|CLNALLE=1
|CLNDBN=Multiple congenital anomalies-hypotonia-seizures syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN077657:614080:280633
|CLNHGVS=NC_000018.9:g.59763135C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606097.0001
|Disease=Multiple congenital anomalies-hypotonia-seizures syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=PIGN:23556
|GENE_ID=23556
|GENE_NAME=PIGN
|REF=C
|RSPOS=59763135
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514475
}}