rs1057520006

Orientation

minus

Stabilized

minus

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

Make rs1057520006(A;A)

Make rs1057520006(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673799

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057520006
dbSNP (classic)	rs1057520006
ClinGen	rs1057520006
ebi	rs1057520006
HLI	rs1057520006
Exac	rs1057520006
Gnomad	rs1057520006
Varsome	rs1057520006
LitVar	rs1057520006
Map	rs1057520006
PheGenI	rs1057520006
Biobank	rs1057520006
1000 genomes	rs1057520006
hgdp	rs1057520006
ensembl	rs1057520006
geneview	rs1057520006
scholar	rs1057520006
google	rs1057520006
pharmgkb	rs1057520006
gwascentral	rs1057520006
openSNP	rs1057520006
23andMe	rs1057520006
SNPshot	rs1057520006
SNPdbe	rs1057520006
MSV3d	rs1057520006
GWAS Ctlg	rs1057520006

Max Magnitude

0

ClinVar
Risk	rs1057520006(A;A) rs1057520006(C;C) rs1057520006(G;G)
Alt	rs1057520006(A;A) rs1057520006(C;C) rs1057520006(G;G)
Reference	Rs1057520006(T;T)
Significance	Probable-Pathogenic
Disease	Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of prostate Malignant melanoma of skin Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Neoplasm of brain Small cell lung cancer Adenocarcinoma of stomach Neoplasm of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of prostate Malignant melanoma of skin Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Neoplasm of brain Small cell lung cancer Adenocarcinoma of stomach Neoplasm of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577117A>C; NC_000017.10:g.7577117A>G; NC_000017.10:g.7577117A>T
CLNSRC
CLNACC	RCV000419865.1, RCV000420544.1, RCV000421122.1, RCV000426446.1, RCV000430539.1, RCV000431168.1, RCV000431803.1, RCV000437117.1, RCV000438367.1, RCV000439046.1, RCV000441279.1, RCV000492506.1, RCV000420150.1, RCV000421817.1, RCV000426067.1, RCV000426772.1, RCV000427353.1, RCV000432482.1, RCV000433292.1, RCV000437438.1, RCV000438006.1, RCV000443517.1, RCV000444136.1, RCV000419239.1, RCV000424200.1, RCV000424885.1, RCV000425563.1, RCV000431443.1, RCV000432106.1, RCV000434236.1, RCV000436477.1, RCV000441480.1, RCV000443016.1, RCV000443884.1,