rs1057519997

Orientation

minus

Stabilized

minus

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

Make rs1057519997(C;C)

Make rs1057519997(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7676037

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519997
dbSNP (classic)	rs1057519997
ClinGen	rs1057519997
ebi	rs1057519997
HLI	rs1057519997
Exac	rs1057519997
Gnomad	rs1057519997
Varsome	rs1057519997
LitVar	rs1057519997
Map	rs1057519997
PheGenI	rs1057519997
Biobank	rs1057519997
1000 genomes	rs1057519997
hgdp	rs1057519997
ensembl	rs1057519997
geneview	rs1057519997
scholar	rs1057519997
google	rs1057519997
pharmgkb	rs1057519997
gwascentral	rs1057519997
openSNP	rs1057519997
23andMe	rs1057519997
SNPshot	rs1057519997
SNPdbe	rs1057519997
MSV3d	rs1057519997
GWAS Ctlg	rs1057519997

Max Magnitude

0

ClinVar
Risk	rs1057519997(A;A) rs1057519997(C;C) rs1057519997(G;G)
Alt	rs1057519997(A;A) rs1057519997(C;C) rs1057519997(G;G)
Reference	Rs1057519997(T;T)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Hepatocellular carcinoma Malignant melanoma of skin Neoplasm of breast Glioblastoma Oesophageal carcinoma Li-Fraumeni syndrome not specified
Variation	info
Gene	TP53
CLNDBN	Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Hepatocellular carcinoma Malignant melanoma of skin Neoplasm of breast Glioblastoma Oesophageal carcinoma Li-Fraumeni syndrome not specified
Reversed	1
HGVS	NC_000017.10:g.7579355A>C; NC_000017.10:g.7579355A>G; NC_000017.10:g.7579355A>T
CLNSRC
CLNACC	RCV000420444.1, RCV000423328.1, RCV000423948.1, RCV000429869.1, RCV000430499.1, RCV000435486.1, RCV000440112.1, RCV000441661.1, RCV000417617.1, RCV000425579.1, RCV000425862.1, RCV000428739.1, RCV000435274.1, RCV000435918.1, RCV000441916.1, RCV000442239.1, RCV000459042.1, RCV000480700.1, RCV000421931.1, RCV000424730.1, RCV000433045.1, RCV000433598.1, RCV000434970.1, RCV000442091.1, RCV000442462.1, RCV000443054.1,