rs1057519994

Orientation

minus

Stabilized

minus

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

Make rs1057519994(C;G)

Make rs1057519994(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674946

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519994
dbSNP (classic)	rs1057519994
ClinGen	rs1057519994
ebi	rs1057519994
HLI	rs1057519994
Exac	rs1057519994
Gnomad	rs1057519994
Varsome	rs1057519994
LitVar	rs1057519994
Map	rs1057519994
PheGenI	rs1057519994
Biobank	rs1057519994
1000 genomes	rs1057519994
hgdp	rs1057519994
ensembl	rs1057519994
geneview	rs1057519994
scholar	rs1057519994
google	rs1057519994
pharmgkb	rs1057519994
gwascentral	rs1057519994
openSNP	rs1057519994
23andMe	rs1057519994
SNPshot	rs1057519994
SNPdbe	rs1057519994
MSV3d	rs1057519994
GWAS Ctlg	rs1057519994

Max Magnitude

0

ClinVar
Risk	rs1057519994(G;G)
Alt	rs1057519994(G;G)
Reference	Rs1057519994(C;C)
Significance	Probable-Pathogenic
Disease	Acute myeloid leukemia Oesophageal carcinoma Neoplasm of brain Ovarian Serous Cystadenocarcinoma Hepatocellular carcinoma Pancreatic adenocarcinoma Uterine Carcinosarcoma Multiple myeloma Neoplasm of breast Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of lung Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Glioblastoma Squamous cell carcinoma of lung
Variation	info
Gene	TP53
CLNDBN	Acute myeloid leukemia Oesophageal carcinoma Neoplasm of brain Ovarian Serous Cystadenocarcinoma Hepatocellular carcinoma Pancreatic adenocarcinoma Uterine Carcinosarcoma Multiple myeloma Neoplasm of breast Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of lung Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Glioblastoma Squamous cell carcinoma of lung
Reversed	1
HGVS	NC_000017.10:g.7578264G>C
CLNSRC
CLNACC	RCV000418858.1, RCV000419550.1, RCV000421371.1, RCV000423525.1, RCV000424140.1, RCV000426409.1, RCV000428127.1, RCV000429158.1, RCV000429834.1, RCV000433822.1, RCV000434462.1, RCV000436566.1, RCV000438380.1, RCV000439382.1, RCV000442092.1, RCV000442140.1,