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rs1642785

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1642785(C;G)
Make rs1642785(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676483
GeneTP53
is asnp
is mentioned by
dbSNPrs1642785
ebirs1642785
HLIrs1642785
Exacrs1642785
Varsomers1642785
Maprs1642785
PheGenIrs1642785
hapmaprs1642785
1000 genomesrs1642785
hgdprs1642785
ensemblrs1642785
gopubmedrs1642785
geneviewrs1642785
scholarrs1642785
googlers1642785
pharmgkbrs1642785
gwascentralrs1642785
openSNPrs1642785
23andMers1642785
23andMe allrs1642785
SNP Nexus

SNPshotrs1642785
SNPdbers1642785
MSV3drs1642785
GWAS Ctlgrs1642785
GMAF0.3636
Max Magnitude0

[PMID 19423538OA-icon.png] Common Genetic Variation in TP53 and Risk of Human Papillomavirus Persistence and Progression to CIN3/Cancer Revisited[PMID 17096406] Germ-line genetic variation of TP53 in osteosarcoma.

[PMID 18798306OA-icon.png] Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.

[PMID 19276375OA-icon.png] Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer.

[PMID 21115003] TP53 polymorphisms in gliomas from Indian patients: Study of codon 72 genotype, rs1642785, rs1800370 and 16 base pair insertion in intron-3.

[PMID 21437228OA-icon.png] Using epidemiology and genomics to understand osteosarcoma etiology.

ClinVar
Risk rs1642785(G;G)
Alt rs1642785(G;G)
Reference rs1642785(C;C)
Significance Non-pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579801G>C
CLNSRC ClinVar GeneDx
CLNACC RCV000125574.2,