{{Rsnum
|rsid=199422218
|Chromosome=17
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AAT)
|geno3=(AAT;AAT)
|Gene=MAPT
|position=46010373
|Gene_s=MAPT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199422218
|Reversed=0
|FwdREF=AAT
|FwdALT=
|REF=TAAT
|ALT=T
|RSPOS=44087738
|CHROM=17
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.44087739_44087741delAAT
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000015334.24; RCV000015335.1
|CLNDBN=Supranuclear palsy, progressive, 1, atypical; Parkinson disease, late-onset, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=157140.0021
|Disease=Supranuclear palsy; Parkinson disease
|GENEINFO=MAPT:4137
|GENE_ID=4137
|GENE_NAME=MAPT
}}