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rs1057519991

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519991(A;G)
Make rs1057519991(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7675076
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519991
dbSNP (old)rs1057519991
ClinGenrs1057519991
ebirs1057519991
HLIrs1057519991
Exacrs1057519991
Gnomadrs1057519991
Varsomers1057519991
Maprs1057519991
PheGenIrs1057519991
Biobankrs1057519991
1000 genomesrs1057519991
hgdprs1057519991
ensemblrs1057519991
gopubmedrs1057519991
geneviewrs1057519991
scholarrs1057519991
googlers1057519991
pharmgkbrs1057519991
gwascentralrs1057519991
openSNPrs1057519991
23andMers1057519991
23andMe allrs1057519991
SNPshotrs1057519991
SNPdbers1057519991
MSV3drs1057519991
GWAS Ctlgrs1057519991
Max Magnitude0
ClinVar
Risk rs1057519991(C;C) rs1057519991(G;G) rs1057519991(T;T)
Alt rs1057519991(C;C) rs1057519991(G;G) rs1057519991(T;T)
Reference Rs1057519991(A;A)
Significance Probable-Pathogenic
Disease Uterine Carcinosarcoma Pancreatic adenocarcinoma Carcinoma of gallbladder Glioblastoma Oesophageal carcinoma Hepatocellular carcinoma Neoplasm of breast Neoplasm of brain Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Malignant melanoma of skin Small cell lung cancer Squamous cell carcinoma of lung Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of lung
Variation info
Gene TP53
CLNDBN Uterine Carcinosarcoma Pancreatic adenocarcinoma Carcinoma of gallbladder Glioblastoma Oesophageal carcinoma Hepatocellular carcinoma Neoplasm of breast Neoplasm of brain Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Malignant melanoma of skin Small cell lung cancer Squamous cell carcinoma of lung Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of lung
Reversed 1
HGVS NC_000017.10:g.7578394T>A; NC_000017.10:g.7578394T>C; NC_000017.10:g.7578394T>G
CLNSRC
CLNACC RCV000418129.1, RCV000418835.1, RCV000420124.1, RCV000421837.1, RCV000426806.1, RCV000427330.1, RCV000427517.1, RCV000427941.1, RCV000429543.1, RCV000432531.1, RCV000432746.1, RCV000433134.1, RCV000435347.1, RCV000438217.1, RCV000438631.1, RCV000439318.1, RCV000439930.1, RCV000443637.1, RCV000444683.1, RCV000417695.1, RCV000417973.1, RCV000420789.1, RCV000421853.1, RCV000423292.1, RCV000426502.1, RCV000427175.1, RCV000428674.1, RCV000429260.1, RCV000432550.1, RCV000433227.1, RCV000433943.1, RCV000437826.1, RCV000438042.1, RCV000438407.1, RCV000439947.1, RCV000440632.1, RCV000443785.1, RCV000445268.1, RCV000420510.1, RCV000421224.1, RCV000421433.1, RCV000422328.1, RCV000426919.1, RCV000427172.1, RCV000427925.1, RCV000428125.1, RCV000431234.1, RCV000432547.1, RCV000433456.1, RCV000434884.1, RCV000437164.1, RCV000438275.1, RCV000439058.1, RCV000441519.1, RCV000443703.1, RCV000444604.1, RCV000444694.1,