rs1057520002

Orientation

minus

Stabilized

minus

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

Make rs1057520002(C;C)

Make rs1057520002(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674242

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057520002
dbSNP (classic)	rs1057520002
ClinGen	rs1057520002
ebi	rs1057520002
HLI	rs1057520002
Exac	rs1057520002
Gnomad	rs1057520002
Varsome	rs1057520002
LitVar	rs1057520002
Map	rs1057520002
PheGenI	rs1057520002
Biobank	rs1057520002
1000 genomes	rs1057520002
hgdp	rs1057520002
ensembl	rs1057520002
geneview	rs1057520002
scholar	rs1057520002
google	rs1057520002
pharmgkb	rs1057520002
gwascentral	rs1057520002
openSNP	rs1057520002
23andMe	rs1057520002
SNPshot	rs1057520002
SNPdbe	rs1057520002
MSV3d	rs1057520002
GWAS Ctlg	rs1057520002

Max Magnitude

0

ClinVar
Risk	rs1057520002(C;C) rs1057520002(G;G)
Alt	rs1057520002(C;C) rs1057520002(G;G)
Reference	Rs1057520002(T;T)
Significance	Probable-Pathogenic
Disease	Oesophageal carcinoma Colorectal Neoplasms Uterine Carcinosarcoma Neoplasm of brain Carcinoma of gallbladder Malignant melanoma of skin Malignant lymphoma Brainstem glioma Malignant neoplasm of body of uterus Neoplasm of breast Glioblastoma Renal cell carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of the head and neck Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Papillary renal cell carcinoma Transitional cell carcinoma of the bladder
Variation	info
Gene	TP53
CLNDBN	Oesophageal carcinoma Colorectal Neoplasms Uterine Carcinosarcoma Neoplasm of brain Carcinoma of gallbladder Malignant melanoma of skin Malignant lymphoma, non-Hodgkin Brainstem glioma Malignant neoplasm of body of uterus Neoplasm of breast Glioblastoma Renal cell carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of the head and neck Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Papillary renal cell carcinoma, sporadic Transitional cell carcinoma of the bladder
Reversed	1
HGVS	NC_000017.10:g.7577560A>C; NC_000017.10:g.7577560A>G
CLNSRC
CLNACC	RCV000418366.1, RCV000419457.1, RCV000420564.1, RCV000422775.1, RCV000423557.1, RCV000424609.1, RCV000425684.1, RCV000426866.1, RCV000429686.1, RCV000432077.1, RCV000434790.1, RCV000434877.1, RCV000435947.1, RCV000437125.1, RCV000440449.1, RCV000441702.1, RCV000441931.1, RCV000441961.1, RCV000443160.1, RCV000417799.1, RCV000418899.1, RCV000421946.1, RCV000422882.1, RCV000423390.1, RCV000425213.1, RCV000427437.1, RCV000428035.1, RCV000429092.1, RCV000430183.1, RCV000433139.1, RCV000433946.1, RCV000435497.1, RCV000436563.1, RCV000437871.1, RCV000439326.1, RCV000442103.1, RCV000442139.1, RCV000443312.1,