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rs1057520006

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520006(A;A)
Make rs1057520006(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673799
GeneTP53
is asnp
is mentioned by
dbSNPrs1057520006
dbSNP (old)rs1057520006
ClinGenrs1057520006
ebirs1057520006
HLIrs1057520006
Exacrs1057520006
Gnomadrs1057520006
Varsomers1057520006
Maprs1057520006
PheGenIrs1057520006
Biobankrs1057520006
1000 genomesrs1057520006
hgdprs1057520006
ensemblrs1057520006
gopubmedrs1057520006
geneviewrs1057520006
scholarrs1057520006
googlers1057520006
pharmgkbrs1057520006
gwascentralrs1057520006
openSNPrs1057520006
23andMers1057520006
23andMe allrs1057520006
SNPshotrs1057520006
SNPdbers1057520006
MSV3drs1057520006
GWAS Ctlgrs1057520006
Max Magnitude0
ClinVar
Risk rs1057520006(A;A) rs1057520006(C;C) rs1057520006(G;G)
Alt rs1057520006(A;A) rs1057520006(C;C) rs1057520006(G;G)
Reference Rs1057520006(T;T)
Significance Probable-Pathogenic
Disease Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of prostate Malignant melanoma of skin Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Neoplasm of brain Small cell lung cancer Adenocarcinoma of stomach Neoplasm of breast Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of prostate Malignant melanoma of skin Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Neoplasm of brain Small cell lung cancer Adenocarcinoma of stomach Neoplasm of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577117A>C; NC_000017.10:g.7577117A>G; NC_000017.10:g.7577117A>T
CLNSRC
CLNACC RCV000419865.1, RCV000420544.1, RCV000421122.1, RCV000426446.1, RCV000430539.1, RCV000431168.1, RCV000431803.1, RCV000437117.1, RCV000438367.1, RCV000439046.1, RCV000441279.1, RCV000492506.1, RCV000420150.1, RCV000421817.1, RCV000426067.1, RCV000426772.1, RCV000427353.1, RCV000432482.1, RCV000433292.1, RCV000437438.1, RCV000438006.1, RCV000443517.1, RCV000444136.1, RCV000419239.1, RCV000424200.1, RCV000424885.1, RCV000425563.1, RCV000431443.1, RCV000432106.1, RCV000434236.1, RCV000436477.1, RCV000441480.1, RCV000443016.1, RCV000443884.1,