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rs1057519982

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519982(A;A)
Make rs1057519982(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674239
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519982
dbSNP (old)rs1057519982
ClinGenrs1057519982
ebirs1057519982
HLIrs1057519982
Exacrs1057519982
Gnomadrs1057519982
Varsomers1057519982
Maprs1057519982
PheGenIrs1057519982
Biobankrs1057519982
1000 genomesrs1057519982
hgdprs1057519982
ensemblrs1057519982
gopubmedrs1057519982
geneviewrs1057519982
scholarrs1057519982
googlers1057519982
pharmgkbrs1057519982
gwascentralrs1057519982
openSNPrs1057519982
23andMers1057519982
23andMe allrs1057519982
SNPshotrs1057519982
SNPdbers1057519982
MSV3drs1057519982
GWAS Ctlgrs1057519982
Max Magnitude0
ClinVar
Risk rs1057519982(A;A) rs1057519982(G;G)
Alt rs1057519982(A;A) rs1057519982(G;G)
Reference Rs1057519982(T;T)
Significance Probable-Pathogenic
Disease Uterine Carcinosarcoma Oesophageal carcinoma Glioblastoma Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Neoplasm of breast Hepatocellular carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Uterine Carcinosarcoma Oesophageal carcinoma Glioblastoma Adenocarcinoma of stomach Chronic lymphocytic leukemia Squamous cell carcinoma of lung Neoplasm of breast Hepatocellular carcinoma Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577557A>C; NC_000017.10:g.7577557A>T
CLNSRC
CLNACC RCV000417900.1, RCV000420803.1, RCV000426704.1, RCV000427357.1, RCV000428013.1, RCV000428578.1, RCV000435223.1, RCV000437385.1, RCV000438030.1, RCV000442190.1, RCV000444807.1, RCV000461418.1, RCV000419559.1, RCV000423712.1, RCV000424356.1, RCV000429187.1, RCV000430244.1, RCV000431566.1, RCV000434352.1, RCV000439881.1, RCV000440943.1, RCV000441578.1, RCV000442629.1,