rs1057519988

Orientation

minus

Stabilized

minus

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

Make rs1057519988(A;A)

Make rs1057519988(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673812

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519988
dbSNP (classic)	rs1057519988
ClinGen	rs1057519988
ebi	rs1057519988
HLI	rs1057519988
Exac	rs1057519988
Gnomad	rs1057519988
Varsome	rs1057519988
LitVar	rs1057519988
Map	rs1057519988
PheGenI	rs1057519988
Biobank	rs1057519988
1000 genomes	rs1057519988
hgdp	rs1057519988
ensembl	rs1057519988
geneview	rs1057519988
scholar	rs1057519988
google	rs1057519988
pharmgkb	rs1057519988
gwascentral	rs1057519988
openSNP	rs1057519988
23andMe	rs1057519988
SNPshot	rs1057519988
SNPdbe	rs1057519988
MSV3d	rs1057519988
GWAS Ctlg	rs1057519988

Max Magnitude

0

ClinVar
Risk	rs1057519988(A;A) rs1057519988(G;G)
Alt	rs1057519988(A;A) rs1057519988(G;G)
Reference	Rs1057519988(T;T)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Oesophageal carcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Neoplasm of brain Ovarian Serous Cystadenocarcinoma Neoplasm of breast
Variation	info
Gene	TP53
CLNDBN	Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Oesophageal carcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Neoplasm of brain Ovarian Serous Cystadenocarcinoma Neoplasm of breast
Reversed	1
HGVS	NC_000017.10:g.7577130A>C; NC_000017.10:g.7577130A>T
CLNSRC
CLNACC	RCV000420461.1, RCV000425222.1, RCV000425855.1, RCV000430671.1, RCV000435260.1, RCV000435460.1, RCV000438306.1, RCV000443062.1, RCV000443210.1, RCV000417655.1, RCV000417883.1, RCV000418371.1, RCV000425994.1, RCV000427865.1, RCV000430718.1, RCV000436003.1, RCV000436185.1, RCV000438999.1,