rs1057519999

Orientation

minus

Stabilized

minus

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

Make rs1057519999(A;G)

Make rs1057519999(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674247

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519999
dbSNP (classic)	rs1057519999
ClinGen	rs1057519999
ebi	rs1057519999
HLI	rs1057519999
Exac	rs1057519999
Gnomad	rs1057519999
Varsome	rs1057519999
LitVar	rs1057519999
Map	rs1057519999
PheGenI	rs1057519999
Biobank	rs1057519999
1000 genomes	rs1057519999
hgdp	rs1057519999
ensembl	rs1057519999
geneview	rs1057519999
scholar	rs1057519999
google	rs1057519999
pharmgkb	rs1057519999
gwascentral	rs1057519999
openSNP	rs1057519999
23andMe	rs1057519999
SNPshot	rs1057519999
SNPdbe	rs1057519999
MSV3d	rs1057519999
GWAS Ctlg	rs1057519999

Max Magnitude

0

ClinVar
Risk	rs1057519999(C;C) rs1057519999(G;G)
Alt	rs1057519999(C;C) rs1057519999(G;G)
Reference	Rs1057519999(A;A)
Significance	Probable-Pathogenic
Disease	Colorectal Neoplasms Renal cell carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Neoplasm of breast Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Adenocarcinoma of stomach Hepatocellular carcinoma Adenocarcinoma of prostate
Variation	info
Gene	TP53
CLNDBN	Colorectal Neoplasms Renal cell carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Neoplasm of breast Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Adenocarcinoma of stomach Hepatocellular carcinoma Adenocarcinoma of prostate
Reversed	1
HGVS	NC_000017.10:g.7577565T>C; NC_000017.10:g.7577565T>G
CLNSRC
CLNACC	RCV000418854.1, RCV000420011.1, RCV000426368.1, RCV000427640.1, RCV000428926.1, RCV000429581.1, RCV000436108.1, RCV000437044.1, RCV000438332.1, RCV000438482.1, RCV000442626.1, RCV000417510.1, RCV000418162.1, RCV000420547.1, RCV000424579.1, RCV000425771.1, RCV000430564.1, RCV000431205.1, RCV000435297.1, RCV000436479.1, RCV000441278.1, RCV000442232.1,