rs1057519986

Orientation

minus

Stabilized

minus

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

Make rs1057519986(C;C)

Make rs1057519986(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673811

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519986
dbSNP (classic)	rs1057519986
ClinGen	rs1057519986
ebi	rs1057519986
HLI	rs1057519986
Exac	rs1057519986
Gnomad	rs1057519986
Varsome	rs1057519986
LitVar	rs1057519986
Map	rs1057519986
PheGenI	rs1057519986
Biobank	rs1057519986
1000 genomes	rs1057519986
hgdp	rs1057519986
ensembl	rs1057519986
geneview	rs1057519986
scholar	rs1057519986
google	rs1057519986
pharmgkb	rs1057519986
gwascentral	rs1057519986
openSNP	rs1057519986
23andMe	rs1057519986
SNPshot	rs1057519986
SNPdbe	rs1057519986
MSV3d	rs1057519986
GWAS Ctlg	rs1057519986

Max Magnitude

0

ClinVar
Risk	rs1057519986(C;C) rs1057519986(G;G)
Alt	rs1057519986(C;C) rs1057519986(G;G)
Reference	Rs1057519986(T;T)
Significance	Probable-Pathogenic
Disease	Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the skin Neoplasm of brain Neoplasm of breast Squamous cell carcinoma of lung Oesophageal carcinoma Squamous cell carcinoma of the head and neck not provided
Variation	info
Gene	TP53
CLNDBN	Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the skin Neoplasm of brain Neoplasm of breast Squamous cell carcinoma of lung Oesophageal carcinoma Squamous cell carcinoma of the head and neck not provided
Reversed	1
HGVS	NC_000017.10:g.7577129A>C; NC_000017.10:g.7577129A>G
CLNSRC
CLNACC	RCV000422121.1, RCV000422786.1, RCV000424190.1, RCV000432351.1, RCV000433925.1, RCV000434574.1, RCV000440467.1, RCV000441020.1, RCV000443933.1, RCV000418965.1, RCV000419602.1, RCV000421032.1, RCV000426140.1, RCV000429016.1, RCV000429241.1, RCV000437299.1, RCV000438621.1, RCV000439252.1, RCV000481465.1,