rs1057520001

Orientation

minus

Stabilized

minus

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

Make rs1057520001(G;G)

Make rs1057520001(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674886

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057520001
dbSNP (classic)	rs1057520001
ClinGen	rs1057520001
ebi	rs1057520001
HLI	rs1057520001
Exac	rs1057520001
Gnomad	rs1057520001
Varsome	rs1057520001
LitVar	rs1057520001
Map	rs1057520001
PheGenI	rs1057520001
Biobank	rs1057520001
1000 genomes	rs1057520001
hgdp	rs1057520001
ensembl	rs1057520001
geneview	rs1057520001
scholar	rs1057520001
google	rs1057520001
pharmgkb	rs1057520001
gwascentral	rs1057520001
openSNP	rs1057520001
23andMe	rs1057520001
SNPshot	rs1057520001
SNPdbe	rs1057520001
MSV3d	rs1057520001
GWAS Ctlg	rs1057520001

Max Magnitude

0

ClinVar
Risk	rs1057520001(G;G)
Alt	rs1057520001(G;G)
Reference	Rs1057520001(T;T)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of stomach Neoplasm of breast Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Small cell lung cancer Hepatocellular carcinoma Oesophageal carcinoma Acute myeloid leukemia Adenocarcinoma of lung Li-Fraumeni syndrome
Variation	info
Gene	TP53
CLNDBN	Adenocarcinoma of stomach Neoplasm of breast Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Small cell lung cancer Hepatocellular carcinoma Oesophageal carcinoma Acute myeloid leukemia Adenocarcinoma of lung Li-Fraumeni syndrome
Reversed	1
HGVS	NC_000017.10:g.7578204A>C
CLNSRC
CLNACC	RCV000421044.1, RCV000422178.1, RCV000425174.1, RCV000431745.1, RCV000432876.1, RCV000437603.1, RCV000439391.1, RCV000442610.1, RCV000442691.1, RCV000465501.1,