rs1057519977

Orientation

minus

Stabilized

minus

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

Make rs1057519977(C;G)

Make rs1057519977(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7675189

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057519977
dbSNP (classic)	rs1057519977
ClinGen	rs1057519977
ebi	rs1057519977
HLI	rs1057519977
Exac	rs1057519977
Gnomad	rs1057519977
Varsome	rs1057519977
LitVar	rs1057519977
Map	rs1057519977
PheGenI	rs1057519977
Biobank	rs1057519977
1000 genomes	rs1057519977
hgdp	rs1057519977
ensembl	rs1057519977
geneview	rs1057519977
scholar	rs1057519977
google	rs1057519977
pharmgkb	rs1057519977
gwascentral	rs1057519977
openSNP	rs1057519977
23andMe	rs1057519977
SNPshot	rs1057519977
SNPdbe	rs1057519977
MSV3d	rs1057519977
GWAS Ctlg	rs1057519977

Max Magnitude

0

ClinVar
Risk	rs1057519977(G;G)
Alt	rs1057519977(G;G)
Reference	Rs1057519977(C;C)
Significance	Probable-Pathogenic
Disease	Colorectal Neoplasms Multiple myeloma Squamous cell carcinoma of lung Acute myeloid leukemia Neoplasm of breast Pancreatic adenocarcinoma Malignant neoplasm of body of uterus Adenocarcinoma of prostate Neoplasm of brain Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Renal cell carcinoma Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Colorectal Neoplasms Multiple myeloma Squamous cell carcinoma of lung Acute myeloid leukemia Neoplasm of breast Pancreatic adenocarcinoma Malignant neoplasm of body of uterus Adenocarcinoma of prostate Neoplasm of brain Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Renal cell carcinoma Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578507G>C
CLNSRC
CLNACC	RCV000422816.1, RCV000423924.1, RCV000424802.1, RCV000425931.1, RCV000430241.1, RCV000431589.1, RCV000434169.1, RCV000434797.1, RCV000440499.1, RCV000442353.1, RCV000444942.1, RCV000445034.1, RCV000467641.1, RCV000492201.1,