rs1057520005

Orientation

minus

Stabilized

minus

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

Make rs1057520005(G;T)

Make rs1057520005(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673800

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057520005
dbSNP (classic)	rs1057520005
ClinGen	rs1057520005
ebi	rs1057520005
HLI	rs1057520005
Exac	rs1057520005
Gnomad	rs1057520005
Varsome	rs1057520005
LitVar	rs1057520005
Map	rs1057520005
PheGenI	rs1057520005
Biobank	rs1057520005
1000 genomes	rs1057520005
hgdp	rs1057520005
ensembl	rs1057520005
geneview	rs1057520005
scholar	rs1057520005
google	rs1057520005
pharmgkb	rs1057520005
gwascentral	rs1057520005
openSNP	rs1057520005
23andMe	rs1057520005
SNPshot	rs1057520005
SNPdbe	rs1057520005
MSV3d	rs1057520005
GWAS Ctlg	rs1057520005

Max Magnitude

0

ClinVar
Risk	rs1057520005(C;C) rs1057520005(T;T)
Alt	rs1057520005(C;C) rs1057520005(T;T)
Reference	Rs1057520005(G;G)
Significance	Probable-Pathogenic
Disease	Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of lung Malignant melanoma of skin Adenocarcinoma of stomach Adenocarcinoma of prostate Small cell lung cancer Neoplasm of brain Neoplasm of breast
Variation	info
Gene	TP53
CLNDBN	Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of lung Malignant melanoma of skin Adenocarcinoma of stomach Adenocarcinoma of prostate Small cell lung cancer Neoplasm of brain Neoplasm of breast
Reversed	1
HGVS	NC_000017.10:g.7577118C>A; NC_000017.10:g.7577118C>G
CLNSRC
CLNACC	RCV000418237.1, RCV000418736.1, RCV000419355.1, RCV000423526.1, RCV000428932.1, RCV000429450.1, RCV000430114.1, RCV000435470.1, RCV000436116.1, RCV000440120.1, RCV000440773.1, RCV000418040.1, RCV000420871.1, RCV000422166.1, RCV000422877.1, RCV000428087.1, RCV000428696.1, RCV000429377.1, RCV000433566.1, RCV000435261.1, RCV000439367.1, RCV000440106.1,