{{Rsnum
|rsid=387906726
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PIGA
|position=15321727
|Gene_s=PIGA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000022881.2
|CLNALLE=1
|CLNDBN=Multiple congenital anomalies-hypotonia-seizures syndrome 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3275508:300868:300496
|CLNHGVS=NC_000023.10:g.15339849G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=311770.0011
|Disease=Multiple congenital anomalies-hypotonia-seizures syndrome 2
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=15339849
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906726
|GENEINFO=PIGA:5277
|GENE_ID=5277
|GENE_NAME=PIGA
}}