{{Rsnum
|rsid = 11540652
|Gene = TP53
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=17
|position=7674220
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TP53
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=LI-FRAUMENI SYNDROME 1
|id=191170
|rsnum=11540652
|variant=0010
}}
{{ neighbor
| rsid = 1042522
| distance = 1934
}}
{{ neighbor
| rsid = 28934571
| distance = 4
}}
{{ neighbor
| rsid = 28934575
| distance = 10
}}

{{ClinVar
|rsid=11540652
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=7577538
|CHROM=17
|dbSNPBuildID=120
|SSR=0
|SAO=3
|VP=0x050368000000000002110120
|GENEINFO=TP53:7157
|GENE_NAME=TP53
|GENE_ID=7157
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.7577538C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=2
|CLNSRCID=191170.0010
|CLNSIG=5
|CLNCUI=C1835398
|CLNDBN=Li-Fraumeni syndrome 1
|Disease=Li-Fraumeni syndrome 1
|CLNACC=RCV000013150.21
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1311:C1835398:151623:524:428850001
}}

{{PMID Auto
|PMID=18798306
|Title=Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.
|OA=1
}}

{{PMID Auto
|PMID=21264207
|Title=Detection of somatic mutations by high-resolution DNA melting (HRM) analysis in multiple cancers.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}