rs587781525

Orientation

minus

Stabilized

minus

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

Make rs587781525(A;G)

Make rs587781525(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7673778

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587781525
dbSNP (classic)	rs587781525
ClinGen	rs587781525
ebi	rs587781525
HLI	rs587781525
Exac	rs587781525
Gnomad	rs587781525
Varsome	rs587781525
LitVar	rs587781525
Map	rs587781525
PheGenI	rs587781525
Biobank	rs587781525
1000 genomes	rs587781525
hgdp	rs587781525
ensembl	rs587781525
geneview	rs587781525
scholar	rs587781525
google	rs587781525
pharmgkb	rs587781525
gwascentral	rs587781525
openSNP	rs587781525
23andMe	rs587781525
SNPshot	rs587781525
SNPdbe	rs587781525
MSV3d	rs587781525
GWAS Ctlg	rs587781525

Max Magnitude

0

ClinVar
Risk	rs587781525(C;C) rs587781525(G;G) rs587781525(T;T)
Alt	rs587781525(C;C) rs587781525(G;G) rs587781525(T;T)
Reference	Rs587781525(A;A)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Chronic lymphocytic leukemia Uterine Carcinosarcoma Ovarian Serous Cystadenocarcinoma Glioblastoma Transitional cell carcinoma of the bladder Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Multiple myeloma Malignant melanoma of skin Renal cell carcinoma Squamous cell carcinoma of the head and neck Neoplasm of breast Adenocarcinoma of stomach Malignant neoplasm of body of uterus Neuroblastoma Squamous cell carcinoma of lung Hepatocellular carcinoma
Variation	info
Gene	TP53
CLNDBN	not provided Hereditary cancer-predisposing syndrome Chronic lymphocytic leukemia Uterine Carcinosarcoma Ovarian Serous Cystadenocarcinoma Glioblastoma Transitional cell carcinoma of the bladder Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Multiple myeloma Malignant melanoma of skin Renal cell carcinoma Squamous cell carcinoma of the head and neck Neoplasm of breast Adenocarcinoma of stomach Malignant neoplasm of body of uterus Neuroblastoma Squamous cell carcinoma of lung Hepatocellular carcinoma
Reversed	1
HGVS	NC_000017.10:g.7577096T>A; NC_000017.10:g.7577096T>C; NC_000017.10:g.7577096T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000161072.1, RCV000215048.1, RCV000417569.1, RCV000418100.1, RCV000423186.1, RCV000423894.1, RCV000425401.1, RCV000426125.1, RCV000428503.1, RCV000431328.1, RCV000432892.1, RCV000433464.1, RCV000434194.1, RCV000435682.1, RCV000435739.1, RCV000438736.1, RCV000440916.1, RCV000441595.1, RCV000442104.1, RCV000443096.1, RCV000129516.2, RCV000418257.1, RCV000418481.1, RCV000423760.1, RCV000423959.1, RCV000425885.1, RCV000426980.1, RCV000428043.1, RCV000429146.1, RCV000431187.1, RCV000433596.1, RCV000434395.1, RCV000435472.1, RCV000436592.1, RCV000436807.1, RCV000438583.1, RCV000441016.1, RCV000442068.1, RCV000442813.1, RCV000417517.1, RCV000419849.1, RCV000420104.1, RCV000422679.1, RCV000424893.1, RCV000425979.1, RCV000427537.1, RCV000429708.1, RCV000430790.1, RCV000433406.1, RCV000435611.1, RCV000435784.1, RCV000438210.1, RCV000440361.1, RCV000440602.1, RCV000442214.1, RCV000442965.1, RCV000443934.1,