Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519995

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519995(A;T)
Make rs1057519995(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674200
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519995
dbSNP (old)rs1057519995
ClinGenrs1057519995
ebirs1057519995
HLIrs1057519995
Exacrs1057519995
Gnomadrs1057519995
Varsomers1057519995
Maprs1057519995
PheGenIrs1057519995
Biobankrs1057519995
1000 genomesrs1057519995
hgdprs1057519995
ensemblrs1057519995
gopubmedrs1057519995
geneviewrs1057519995
scholarrs1057519995
googlers1057519995
pharmgkbrs1057519995
gwascentralrs1057519995
openSNPrs1057519995
23andMers1057519995
23andMe allrs1057519995
SNPshotrs1057519995
SNPdbers1057519995
MSV3drs1057519995
GWAS Ctlgrs1057519995
Max Magnitude0
ClinVar
Risk rs1057519995(T;T)
Alt rs1057519995(T;T)
Reference Rs1057519995(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of brain Adenocarcinoma of lung Neoplasm of breast Glioblastoma Oesophageal carcinoma Chronic lymphocytic leukemia Pancreatic adenocarcinoma
Variation info
Gene TP53
CLNDBN Neoplasm of brain Adenocarcinoma of lung Neoplasm of breast Glioblastoma Oesophageal carcinoma Chronic lymphocytic leukemia Pancreatic adenocarcinoma
Reversed 1
HGVS NC_000017.10:g.7577518T>A
CLNSRC
CLNACC RCV000418615.1, RCV000425759.1, RCV000428426.1, RCV000435616.1, RCV000436027.1, RCV000436676.1, RCV000444896.1,