{{Rsnum
|rsid=121918521
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP6AP2
|position=40597269
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP6AP2
}}{{omim
|id=300556
|rsnum=121918521
|variant=0001
}}{{ClinVar
|rsid=121918521
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=40456521
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ATP6AP2:10159
|GENE_NAME=ATP6AP2
|GENE_ID=10159
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.40456521C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300556.0001
|CLNSIG=5
|CLNCUI=C1845543
|CLNDBN=Mental retardation, X-linked, syndromic, Hedera type
|Disease=Mental retardation
|CLNACC=RCV000011548.3
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845543:300423:2076
}}