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rs786201838

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201838(A;G)
Make rs786201838(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674953
GeneTP53
is asnp
is mentioned by
dbSNPrs786201838
dbSNP (old)rs786201838
ClinGenrs786201838
ebirs786201838
HLIrs786201838
Exacrs786201838
Gnomadrs786201838
Varsomers786201838
Maprs786201838
PheGenIrs786201838
Biobankrs786201838
1000 genomesrs786201838
hgdprs786201838
ensemblrs786201838
gopubmedrs786201838
geneviewrs786201838
scholarrs786201838
googlers786201838
pharmgkbrs786201838
gwascentralrs786201838
openSNPrs786201838
23andMers786201838
23andMe allrs786201838
SNP Nexus

SNPshotrs786201838
SNPdbers786201838
MSV3drs786201838
GWAS Ctlgrs786201838
Max Magnitude0
ClinVar
Risk rs786201838(C;C) rs786201838(G;G) rs786201838(T;T)
Alt rs786201838(C;C) rs786201838(G;G) rs786201838(T;T)
Reference Rs786201838(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Oesophageal carcinoma Squamous cell carcinoma of the head and neck Small cell lung cancer Chronic lymphocytic leukemia Adenocarcinoma of prostate Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Brainstem glioma Squamous cell carcinoma of lung Colorectal Neoplasms Neoplasm of breast Acute myeloid leukemia Uterine Carcinosarcoma Pancreatic adenocarcinoma Papillary renal cell carcinoma Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Neoplasm of brain Hepatocellular carcinoma Adenocarcinoma of stomach not provided Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Oesophageal carcinoma Squamous cell carcinoma of the head and neck Small cell lung cancer Chronic lymphocytic leukemia Adenocarcinoma of prostate Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Brainstem glioma Squamous cell carcinoma of lung Colorectal Neoplasms Neoplasm of breast Acute myeloid leukemia Uterine Carcinosarcoma Pancreatic adenocarcinoma Papillary renal cell carcinoma, sporadic Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Neoplasm of brain Hepatocellular carcinoma Adenocarcinoma of stomach not provided Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578271T>A; NC_000017.10:g.7578271T>C; NC_000017.10:g.7578271T>G
CLNSRC UniProtKB (protein)
CLNACC RCV000165315.1, RCV000419701.1, RCV000420523.1, RCV000421145.1, RCV000421777.1, RCV000422830.1, RCV000426960.1, RCV000427615.1, RCV000428359.1, RCV000430839.1, RCV000431198.1, RCV000432479.1, RCV000433537.1, RCV000437609.1, RCV000437660.1, RCV000438323.1, RCV000438373.1, RCV000439007.1, RCV000441921.1, RCV000443734.1, RCV000444673.1, RCV000164329.1, RCV000255425.1, RCV000417979.1, RCV000418086.1, RCV000418288.1, RCV000423052.1, RCV000423280.1, RCV000424475.1, RCV000425611.1, RCV000427767.1, RCV000428340.1, RCV000429618.1, RCV000433342.1, RCV000434391.1, RCV000434549.1, RCV000435651.1, RCV000435870.1, RCV000439433.1, RCV000439827.1, RCV000440903.1, RCV000445029.1, RCV000445148.1, RCV000460847.1, RCV000417520.1, RCV000418213.1, RCV000422374.1, RCV000422912.1, RCV000423516.1, RCV000424851.1, RCV000427668.1, RCV000428197.1, RCV000428877.1, RCV000429577.1, RCV000433585.1, RCV000434205.1, RCV000434933.1, RCV000435420.1, RCV000435566.1, RCV000439568.1, RCV000440128.1, RCV000442541.1, RCV000444985.1, RCV000445292.1,