rs1057519991

Orientation

minus

Stabilized

minus

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

Make rs1057519991(A;G)

Make rs1057519991(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7675076

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519991
dbSNP (classic)	rs1057519991
ClinGen	rs1057519991
ebi	rs1057519991
HLI	rs1057519991
Exac	rs1057519991
Gnomad	rs1057519991
Varsome	rs1057519991
LitVar	rs1057519991
Map	rs1057519991
PheGenI	rs1057519991
Biobank	rs1057519991
1000 genomes	rs1057519991
hgdp	rs1057519991
ensembl	rs1057519991
geneview	rs1057519991
scholar	rs1057519991
google	rs1057519991
pharmgkb	rs1057519991
gwascentral	rs1057519991
openSNP	rs1057519991
23andMe	rs1057519991
SNPshot	rs1057519991
SNPdbe	rs1057519991
MSV3d	rs1057519991
GWAS Ctlg	rs1057519991

Max Magnitude

0

ClinVar
Risk	rs1057519991(C;C) rs1057519991(G;G) rs1057519991(T;T)
Alt	rs1057519991(C;C) rs1057519991(G;G) rs1057519991(T;T)
Reference	Rs1057519991(A;A)
Significance	Probable-Pathogenic
Disease	Uterine Carcinosarcoma Pancreatic adenocarcinoma Carcinoma of gallbladder Glioblastoma Oesophageal carcinoma Hepatocellular carcinoma Neoplasm of breast Neoplasm of brain Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Malignant melanoma of skin Small cell lung cancer Squamous cell carcinoma of lung Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of lung
Variation	info
Gene	TP53
CLNDBN	Uterine Carcinosarcoma Pancreatic adenocarcinoma Carcinoma of gallbladder Glioblastoma Oesophageal carcinoma Hepatocellular carcinoma Neoplasm of breast Neoplasm of brain Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Malignant melanoma of skin Small cell lung cancer Squamous cell carcinoma of lung Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of lung
Reversed	1
HGVS	NC_000017.10:g.7578394T>A; NC_000017.10:g.7578394T>C; NC_000017.10:g.7578394T>G
CLNSRC
CLNACC	RCV000418129.1, RCV000418835.1, RCV000420124.1, RCV000421837.1, RCV000426806.1, RCV000427330.1, RCV000427517.1, RCV000427941.1, RCV000429543.1, RCV000432531.1, RCV000432746.1, RCV000433134.1, RCV000435347.1, RCV000438217.1, RCV000438631.1, RCV000439318.1, RCV000439930.1, RCV000443637.1, RCV000444683.1, RCV000417695.1, RCV000417973.1, RCV000420789.1, RCV000421853.1, RCV000423292.1, RCV000426502.1, RCV000427175.1, RCV000428674.1, RCV000429260.1, RCV000432550.1, RCV000433227.1, RCV000433943.1, RCV000437826.1, RCV000438042.1, RCV000438407.1, RCV000439947.1, RCV000440632.1, RCV000443785.1, RCV000445268.1, RCV000420510.1, RCV000421224.1, RCV000421433.1, RCV000422328.1, RCV000426919.1, RCV000427172.1, RCV000427925.1, RCV000428125.1, RCV000431234.1, RCV000432547.1, RCV000433456.1, RCV000434884.1, RCV000437164.1, RCV000438275.1, RCV000439058.1, RCV000441519.1, RCV000443703.1, RCV000444604.1, RCV000444694.1,