rs1057519980

Orientation

minus

Stabilized

minus

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

Make rs1057519980(C;G)

Make rs1057519980(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7675084

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519980
dbSNP (classic)	rs1057519980
ClinGen	rs1057519980
ebi	rs1057519980
HLI	rs1057519980
Exac	rs1057519980
Gnomad	rs1057519980
Varsome	rs1057519980
LitVar	rs1057519980
Map	rs1057519980
PheGenI	rs1057519980
Biobank	rs1057519980
1000 genomes	rs1057519980
hgdp	rs1057519980
ensembl	rs1057519980
geneview	rs1057519980
scholar	rs1057519980
google	rs1057519980
pharmgkb	rs1057519980
gwascentral	rs1057519980
openSNP	rs1057519980
23andMe	rs1057519980
SNPshot	rs1057519980
SNPdbe	rs1057519980
MSV3d	rs1057519980
GWAS Ctlg	rs1057519980

Max Magnitude

0

ClinVar
Risk	rs1057519980(G;G)
Alt	rs1057519980(G;G)
Reference	Rs1057519980(C;C)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Adenocarcinoma of stomach Oesophageal carcinoma Renal cell carcinoma Neoplasm of brain Transitional cell carcinoma of the bladder Colorectal Neoplasms Hepatocellular carcinoma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Neoplasm of breast Pancreatic adenocarcinoma Squamous cell carcinoma of lung Acute myeloid leukemia
Variation	info
Gene	TP53
CLNDBN	Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Adenocarcinoma of stomach Oesophageal carcinoma Renal cell carcinoma Neoplasm of brain Transitional cell carcinoma of the bladder Colorectal Neoplasms Hepatocellular carcinoma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Neoplasm of breast Pancreatic adenocarcinoma Squamous cell carcinoma of lung Acute myeloid leukemia
Reversed	1
HGVS	NC_000017.10:g.7578402G>C
CLNSRC
CLNACC	RCV000418563.1, RCV000421434.1, RCV000422732.1, RCV000424249.1, RCV000424653.1, RCV000429475.1, RCV000429952.1, RCV000430137.1, RCV000432087.1, RCV000434070.1, RCV000439276.1, RCV000440822.1, RCV000441518.1, RCV000442369.1, RCV000445065.1,