rs1057519987

Orientation

minus

Stabilized

minus

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

Make rs1057519987(G;G)

Make rs1057519987(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673810

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519987
dbSNP (classic)	rs1057519987
ClinGen	rs1057519987
ebi	rs1057519987
HLI	rs1057519987
Exac	rs1057519987
Gnomad	rs1057519987
Varsome	rs1057519987
LitVar	rs1057519987
Map	rs1057519987
PheGenI	rs1057519987
Biobank	rs1057519987
1000 genomes	rs1057519987
hgdp	rs1057519987
ensembl	rs1057519987
geneview	rs1057519987
scholar	rs1057519987
google	rs1057519987
pharmgkb	rs1057519987
gwascentral	rs1057519987
openSNP	rs1057519987
23andMe	rs1057519987
SNPshot	rs1057519987
SNPdbe	rs1057519987
MSV3d	rs1057519987
GWAS Ctlg	rs1057519987

Max Magnitude

0

ClinVar
Risk	rs1057519987(G;G)
Alt	rs1057519987(G;G)
Reference	Rs1057519987(T;T)
Significance	Probable-Pathogenic
Disease	Neoplasm of breast Neoplasm of brain Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Adenocarcinoma of stomach Adenocarcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Variation	info
Gene	TP53
CLNDBN	Neoplasm of breast Neoplasm of brain Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Adenocarcinoma of stomach Adenocarcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Reversed	1
HGVS	NC_000017.10:g.7577128A>C
CLNSRC
CLNACC	RCV000423824.1, RCV000426445.1, RCV000426634.1, RCV000432152.1, RCV000433231.1, RCV000434093.1, RCV000438906.1, RCV000442796.1, RCV000443660.1,