rs1057519976

Orientation

minus

Stabilized

minus

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

Make rs1057519976(C;G)

Make rs1057519976(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7675207

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519976
dbSNP (classic)	rs1057519976
ClinGen	rs1057519976
ebi	rs1057519976
HLI	rs1057519976
Exac	rs1057519976
Gnomad	rs1057519976
Varsome	rs1057519976
LitVar	rs1057519976
Map	rs1057519976
PheGenI	rs1057519976
Biobank	rs1057519976
1000 genomes	rs1057519976
hgdp	rs1057519976
ensembl	rs1057519976
geneview	rs1057519976
scholar	rs1057519976
google	rs1057519976
pharmgkb	rs1057519976
gwascentral	rs1057519976
openSNP	rs1057519976
23andMe	rs1057519976
SNPshot	rs1057519976
SNPdbe	rs1057519976
MSV3d	rs1057519976
GWAS Ctlg	rs1057519976

Max Magnitude

0

ClinVar
Risk	rs1057519976(G;G)
Alt	rs1057519976(G;G)
Reference	Rs1057519976(C;C)
Significance	Probable-Pathogenic
Disease	Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of lung Adrenocortical carcinoma Adenocarcinoma of prostate Neoplasm of brain Neoplasm of breast Colorectal Neoplasms Transitional cell carcinoma of the bladder Squamous cell carcinoma of lung Adenocarcinoma of stomach not specified
Variation	info
Gene	TP53
CLNDBN	Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of lung Adrenocortical carcinoma Adenocarcinoma of prostate Neoplasm of brain Neoplasm of breast Colorectal Neoplasms Transitional cell carcinoma of the bladder Squamous cell carcinoma of lung Adenocarcinoma of stomach not specified
Reversed	1
HGVS	NC_000017.10:g.7578525G>C
CLNSRC
CLNACC	RCV000417767.1, RCV000420220.1, RCV000420893.1, RCV000423274.1, RCV000424924.1, RCV000429841.1, RCV000430892.1, RCV000432245.1, RCV000434979.1, RCV000435704.1, RCV000439451.1, RCV000440498.1, RCV000441628.1, RCV000479510.1,