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rs1057519987

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519987(G;G)
Make rs1057519987(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673810
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519987
dbSNP (old)rs1057519987
ClinGenrs1057519987
ebirs1057519987
HLIrs1057519987
Exacrs1057519987
Gnomadrs1057519987
Varsomers1057519987
LitVarrs1057519987
Maprs1057519987
PheGenIrs1057519987
Biobankrs1057519987
1000 genomesrs1057519987
hgdprs1057519987
ensemblrs1057519987
gopubmedrs1057519987
geneviewrs1057519987
scholarrs1057519987
googlers1057519987
pharmgkbrs1057519987
gwascentralrs1057519987
openSNPrs1057519987
23andMers1057519987
23andMe allrs1057519987
SNPshotrs1057519987
SNPdbers1057519987
MSV3drs1057519987
GWAS Ctlgrs1057519987
Max Magnitude0
ClinVar
Risk rs1057519987(G;G)
Alt rs1057519987(G;G)
Reference Rs1057519987(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of breast Neoplasm of brain Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Adenocarcinoma of stomach Adenocarcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Variation info
Gene TP53
CLNDBN Neoplasm of breast Neoplasm of brain Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Adenocarcinoma of stomach Adenocarcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Reversed 1
HGVS NC_000017.10:g.7577128A>C
CLNSRC
CLNACC RCV000423824.1, RCV000426445.1, RCV000426634.1, RCV000432152.1, RCV000433231.1, RCV000434093.1, RCV000438906.1, RCV000442796.1, RCV000443660.1,