rs1057519995

Orientation

minus

Stabilized

minus

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

Make rs1057519995(A;T)

Make rs1057519995(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674200

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519995
dbSNP (classic)	rs1057519995
ClinGen	rs1057519995
ebi	rs1057519995
HLI	rs1057519995
Exac	rs1057519995
Gnomad	rs1057519995
Varsome	rs1057519995
LitVar	rs1057519995
Map	rs1057519995
PheGenI	rs1057519995
Biobank	rs1057519995
1000 genomes	rs1057519995
hgdp	rs1057519995
ensembl	rs1057519995
geneview	rs1057519995
scholar	rs1057519995
google	rs1057519995
pharmgkb	rs1057519995
gwascentral	rs1057519995
openSNP	rs1057519995
23andMe	rs1057519995
SNPshot	rs1057519995
SNPdbe	rs1057519995
MSV3d	rs1057519995
GWAS Ctlg	rs1057519995

Max Magnitude

0

ClinVar
Risk	rs1057519995(T;T)
Alt	rs1057519995(T;T)
Reference	Rs1057519995(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm of brain Adenocarcinoma of lung Neoplasm of breast Glioblastoma Oesophageal carcinoma Chronic lymphocytic leukemia Pancreatic adenocarcinoma
Variation	info
Gene	TP53
CLNDBN	Neoplasm of brain Adenocarcinoma of lung Neoplasm of breast Glioblastoma Oesophageal carcinoma Chronic lymphocytic leukemia Pancreatic adenocarcinoma
Reversed	1
HGVS	NC_000017.10:g.7577518T>A
CLNSRC
CLNACC	RCV000418615.1, RCV000425759.1, RCV000428426.1, RCV000435616.1, RCV000436027.1, RCV000436676.1, RCV000444896.1,