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rs587778720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778720(A;A)
Make rs587778720(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674893
GeneTP53
is asnp
is mentioned by
dbSNPrs587778720
dbSNP (old)rs587778720
ClinGenrs587778720
ebirs587778720
HLIrs587778720
Exacrs587778720
Varsomers587778720
Maprs587778720
PheGenIrs587778720
Biobankrs587778720
1000 genomesrs587778720
hgdprs587778720
ensemblrs587778720
gopubmedrs587778720
geneviewrs587778720
scholarrs587778720
googlers587778720
pharmgkbrs587778720
gwascentralrs587778720
openSNPrs587778720
23andMers587778720
23andMe allrs587778720
SNP Nexus

SNPshotrs587778720
SNPdbers587778720
MSV3drs587778720
GWAS Ctlgrs587778720
Max Magnitude0
ClinVar
Risk rs587778720(A;A) rs587778720(C;C) rs587778720(T;T)
Alt rs587778720(A;A) rs587778720(C;C) rs587778720(T;T)
Reference Rs587778720(G;G)
Significance Pathogenic
Disease Adrenocortical carcinoma Uterine Carcinosarcoma Malignant melanoma of skin Neoplasm of brain Colorectal Neoplasms Hepatocellular carcinoma Glioblastoma Pancreatic adenocarcinoma Renal cell carcinoma Neoplasm of breast Oesophageal carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Adenoid cystic carcinoma Adenocarcinoma of prostate Adenocarcinoma of lung Nasopharyngeal Neoplasms Ovarian Serous Cystadenocarcinoma Malignant neoplasm of body of uterus Hereditary cancer-predisposing syndrome not specified Li-Fraumeni syndrome Li-Fraumeni syndrome 1 not provided
Variation info
Gene TP53
CLNDBN Adrenocortical carcinoma Uterine Carcinosarcoma Malignant melanoma of skin Neoplasm of brain Colorectal Neoplasms Hepatocellular carcinoma Glioblastoma Pancreatic adenocarcinoma Renal cell carcinoma Neoplasm of breast Oesophageal carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Adenoid cystic carcinoma Adenocarcinoma of prostate Adenocarcinoma of lung Nasopharyngeal Neoplasms Ovarian Serous Cystadenocarcinoma Malignant neoplasm of body of uterus Hereditary cancer-predisposing syndrome not specified Li-Fraumeni syndrome Li-Fraumeni syndrome 1 not provided
Reversed 1
HGVS NC_000017.10:g.7578211C>A; NC_000017.10:g.7578211C>G; NC_000017.10:g.7578211C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000417467.1, RCV000418608.1, RCV000418814.1, RCV000421737.1, RCV000422458.1, RCV000422684.1, RCV000427240.1, RCV000427500.1, RCV000428488.1, RCV000428624.1, RCV000428841.1, RCV000432738.1, RCV000433789.1, RCV000435132.1, RCV000435387.1, RCV000437481.1, RCV000438469.1, RCV000439587.1, RCV000439979.1, RCV000443648.1, RCV000444469.1, RCV000445195.1, RCV000220461.2, RCV000418520.1, RCV000419521.1, RCV000420213.1, RCV000423147.1, RCV000423776.1, RCV000424407.1, RCV000425014.1, RCV000426111.1, RCV000429975.1, RCV000430230.1, RCV000430895.1, RCV000431639.1, RCV000433848.1, RCV000434458.1, RCV000435742.1, RCV000436779.1, RCV000440212.1, RCV000440917.1, RCV000441029.1, RCV000441598.1, RCV000443850.1, RCV000443926.1, RCV000122176.1, RCV000123099.3, RCV000130072.4, RCV000144664.1, RCV000419636.1, RCV000420459.1, RCV000420595.1, RCV000420734.1, RCV000420908.1, RCV000422008.1, RCV000424188.1, RCV000425846.1, RCV000427005.1, RCV000428223.1, RCV000430601.1, RCV000430755.1, RCV000430946.1, RCV000432016.1, RCV000432438.1, RCV000436981.1, RCV000437236.1, RCV000438230.1, RCV000438582.1, RCV000441015.1, RCV000443346.1, RCV000444077.1, RCV000444201.1,