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rs1057520001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520001(G;G)
Make rs1057520001(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674886
GeneTP53
is asnp
is mentioned by
dbSNPrs1057520001
dbSNP (old)rs1057520001
ClinGenrs1057520001
ebirs1057520001
HLIrs1057520001
Exacrs1057520001
Gnomadrs1057520001
Varsomers1057520001
LitVarrs1057520001
Maprs1057520001
PheGenIrs1057520001
Biobankrs1057520001
1000 genomesrs1057520001
hgdprs1057520001
ensemblrs1057520001
gopubmedrs1057520001
geneviewrs1057520001
scholarrs1057520001
googlers1057520001
pharmgkbrs1057520001
gwascentralrs1057520001
openSNPrs1057520001
23andMers1057520001
23andMe allrs1057520001
SNPshotrs1057520001
SNPdbers1057520001
MSV3drs1057520001
GWAS Ctlgrs1057520001
Max Magnitude0
ClinVar
Risk rs1057520001(G;G)
Alt rs1057520001(G;G)
Reference Rs1057520001(T;T)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Neoplasm of breast Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Small cell lung cancer Hepatocellular carcinoma Oesophageal carcinoma Acute myeloid leukemia Adenocarcinoma of lung Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Adenocarcinoma of stomach Neoplasm of breast Ovarian Serous Cystadenocarcinoma Pancreatic adenocarcinoma Small cell lung cancer Hepatocellular carcinoma Oesophageal carcinoma Acute myeloid leukemia Adenocarcinoma of lung Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578204A>C
CLNSRC
CLNACC RCV000421044.1, RCV000422178.1, RCV000425174.1, RCV000431745.1, RCV000432876.1, RCV000437603.1, RCV000439391.1, RCV000442610.1, RCV000442691.1, RCV000465501.1,