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rs587781525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781525(A;G)
Make rs587781525(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673778
GeneTP53
is asnp
is mentioned by
dbSNPrs587781525
ClinGenrs587781525
ebirs587781525
HLIrs587781525
Exacrs587781525
Varsomers587781525
Maprs587781525
PheGenIrs587781525
hapmaprs587781525
1000 genomesrs587781525
hgdprs587781525
ensemblrs587781525
gopubmedrs587781525
geneviewrs587781525
scholarrs587781525
googlers587781525
pharmgkbrs587781525
gwascentralrs587781525
openSNPrs587781525
23andMers587781525
23andMe allrs587781525
SNP Nexus

SNPshotrs587781525
SNPdbers587781525
MSV3drs587781525
GWAS Ctlgrs587781525
Max Magnitude0
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,