rs1057519983

Orientation

minus

Stabilized

minus

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

Make rs1057519983(C;C)

Make rs1057519983(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673797

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519983
dbSNP (classic)	rs1057519983
ClinGen	rs1057519983
ebi	rs1057519983
HLI	rs1057519983
Exac	rs1057519983
Gnomad	rs1057519983
Varsome	rs1057519983
LitVar	rs1057519983
Map	rs1057519983
PheGenI	rs1057519983
Biobank	rs1057519983
1000 genomes	rs1057519983
hgdp	rs1057519983
ensembl	rs1057519983
geneview	rs1057519983
scholar	rs1057519983
google	rs1057519983
pharmgkb	rs1057519983
gwascentral	rs1057519983
openSNP	rs1057519983
23andMe	rs1057519983
SNPshot	rs1057519983
SNPdbe	rs1057519983
MSV3d	rs1057519983
GWAS Ctlg	rs1057519983

Max Magnitude

0

ClinVar
Risk	rs1057519983(C;C)
Alt	rs1057519983(C;C)
Reference	Rs1057519983(T;T)
Significance	Probable-Pathogenic
Disease	Neoplasm of brain Neoplasm of breast Hepatocellular carcinoma Multiple myeloma Colorectal Neoplasms Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Renal cell carcinoma Adenocarcinoma of lung Oesophageal carcinoma Glioblastoma Malignant melanoma of skin Adrenocortical carcinoma Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma
Variation	info
Gene	TP53
CLNDBN	Neoplasm of brain Neoplasm of breast Hepatocellular carcinoma Multiple myeloma Colorectal Neoplasms Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Renal cell carcinoma Adenocarcinoma of lung Oesophageal carcinoma Glioblastoma Malignant melanoma of skin Adrenocortical carcinoma Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma
Reversed	1
HGVS	NC_000017.10:g.7577115A>G
CLNSRC
CLNACC	RCV000418020.1, RCV000420225.1, RCV000420853.1, RCV000424757.1, RCV000425483.1, RCV000426139.1, RCV000430390.1, RCV000431136.1, RCV000432909.1, RCV000433579.1, RCV000435015.1, RCV000435695.1, RCV000440640.1, RCV000441393.1, RCV000442259.1, RCV000443110.1,