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rs1057519997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519997(C;C)
Make rs1057519997(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7676037
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519997
dbSNP (old)rs1057519997
ClinGenrs1057519997
ebirs1057519997
HLIrs1057519997
Exacrs1057519997
Gnomadrs1057519997
Varsomers1057519997
Maprs1057519997
PheGenIrs1057519997
Biobankrs1057519997
1000 genomesrs1057519997
hgdprs1057519997
ensemblrs1057519997
gopubmedrs1057519997
geneviewrs1057519997
scholarrs1057519997
googlers1057519997
pharmgkbrs1057519997
gwascentralrs1057519997
openSNPrs1057519997
23andMers1057519997
23andMe allrs1057519997
SNPshotrs1057519997
SNPdbers1057519997
MSV3drs1057519997
GWAS Ctlgrs1057519997
Max Magnitude0
ClinVar
Risk rs1057519997(A;A) rs1057519997(C;C) rs1057519997(G;G)
Alt rs1057519997(A;A) rs1057519997(C;C) rs1057519997(G;G)
Reference Rs1057519997(T;T)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Hepatocellular carcinoma Malignant melanoma of skin Neoplasm of breast Glioblastoma Oesophageal carcinoma Li-Fraumeni syndrome not specified
Variation info
Gene TP53
CLNDBN Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Hepatocellular carcinoma Malignant melanoma of skin Neoplasm of breast Glioblastoma Oesophageal carcinoma Li-Fraumeni syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7579355A>C; NC_000017.10:g.7579355A>G; NC_000017.10:g.7579355A>T
CLNSRC
CLNACC RCV000420444.1, RCV000423328.1, RCV000423948.1, RCV000429869.1, RCV000430499.1, RCV000435486.1, RCV000440112.1, RCV000441661.1, RCV000417617.1, RCV000425579.1, RCV000425862.1, RCV000428739.1, RCV000435274.1, RCV000435918.1, RCV000441916.1, RCV000442239.1, RCV000459042.1, RCV000480700.1, RCV000421931.1, RCV000424730.1, RCV000433045.1, RCV000433598.1, RCV000434970.1, RCV000442091.1, RCV000442462.1, RCV000443054.1,