rs1642785

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1642785(C;G)

Make rs1642785(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7676483

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1642785
dbSNP (classic)	rs1642785
ClinGen	rs1642785
ebi	rs1642785
HLI	rs1642785
Exac	rs1642785
Gnomad	rs1642785
Varsome	rs1642785
LitVar	rs1642785
Map	rs1642785
PheGenI	rs1642785
Biobank	rs1642785
1000 genomes	rs1642785
hgdp	rs1642785
ensembl	rs1642785
geneview	rs1642785
scholar	rs1642785
google	rs1642785
pharmgkb	rs1642785
gwascentral	rs1642785
openSNP	rs1642785
23andMe	rs1642785
SNPshot	rs1642785
SNPdbe	rs1642785
MSV3d	rs1642785
GWAS Ctlg	rs1642785

GMAF

0.3636

Max Magnitude

0

[PMID 19423538 ] 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 18798306 ] 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 19276375 ] 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 21437228 ] Using epidemiology and genomics to understand osteosarcoma etiology.

ClinVar
Risk	rs1642785(A;A) rs1642785(G;G)
Alt	rs1642785(A;A) rs1642785(G;G)
Reference	Rs1642785(C;C)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	TP53
CLNDBN	not specified
Reversed	1
HGVS	NC_000017.10:g.7579801G>C
CLNSRC	ClinVar GeneDx
CLNACC	RCV000250671.1,