{{Rsnum
|rsid=63750959
|Gene=MAPT
|Chromosome=17
|position=45962351
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAPT
}}{{omim
|id=157140
|rsnum=63750959
|variant=0017
}}
{{omim
|id=157140
|rsnum=63750959
|variant=0019
}}{{ClinVar
|rsid=63750959
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=44039717
|CHROM=17
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x05016000000004001e110100
|GENEINFO=MAPT:4137
|GENE_NAME=MAPT
|GENE_ID=4137
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.44039717G>A; NC_000017.10:g.44039717G>T
|CLNSRC=OMIM Allelic Variant; Neurodegenerative Brain Diseases Group
|CLNORIGIN=1
|CLNSRCID=157140.0017; ADM_173; 157140.0019
|CLNSIG=5
|CLNCUI=C0338451; C0038868
|CLNDBN=Frontotemporal dementia; Progressive supranuclear ophthalmoplegia; not provided
|Disease=Frontotemporal dementia; Progressive supranuclear ophthalmoplegia; not provided
|CLNACC=RCV000015330.24; RCV000015332.24; RCV000084498.1
|Tags=PM;SLO;VLD;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1505:C0338451:600274:282:230270009; NBK1505:C0038868:601104:240071:28978003
|COMMON=1
}}