Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519981(C;C)
Make rs1057519981(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674251
GeneTP53
is asnp
is mentioned by
dbSNPrs1057519981
dbSNP (old)rs1057519981
ClinGenrs1057519981
ebirs1057519981
HLIrs1057519981
Exacrs1057519981
Gnomadrs1057519981
Varsomers1057519981
LitVarrs1057519981
Maprs1057519981
PheGenIrs1057519981
Biobankrs1057519981
1000 genomesrs1057519981
hgdprs1057519981
ensemblrs1057519981
gopubmedrs1057519981
geneviewrs1057519981
scholarrs1057519981
googlers1057519981
pharmgkbrs1057519981
gwascentralrs1057519981
openSNPrs1057519981
23andMers1057519981
23andMe allrs1057519981
SNPshotrs1057519981
SNPdbers1057519981
MSV3drs1057519981
GWAS Ctlgrs1057519981
Max Magnitude0
ClinVar
Risk rs1057519981(C;C) rs1057519981(G;G)
Alt rs1057519981(C;C) rs1057519981(G;G)
Reference Rs1057519981(T;T)
Significance Pathogenic
Disease Adenocarcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Uterine cervical neoplasms Transitional cell carcinoma of the bladder Colorectal Neoplasms Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Multiple myeloma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Neoplasm of brain Hepatocellular carcinoma Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Adenocarcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Uterine cervical neoplasms Transitional cell carcinoma of the bladder Colorectal Neoplasms Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Multiple myeloma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Neoplasm of brain Hepatocellular carcinoma Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577569A>C; NC_000017.10:g.7577569A>G
CLNSRC
CLNACC RCV000417486.1, RCV000420677.1, RCV000422044.1, RCV000422283.1, RCV000423396.1, RCV000427246.1, RCV000428630.1, RCV000428804.1, RCV000430919.1, RCV000433478.1, RCV000435170.1, RCV000437321.1, RCV000437476.1, RCV000438876.1, RCV000439946.1, RCV000443356.1, RCV000444792.1, RCV000419348.1, RCV000420409.1, RCV000421679.1, RCV000421933.1, RCV000424052.1, RCV000426193.1, RCV000428210.1, RCV000430482.1, RCV000430655.1, RCV000431946.1, RCV000433046.1, RCV000437018.1, RCV000437199.1, RCV000438447.1, RCV000441834.1, RCV000441879.1, RCV000442237.1, RCV000492666.1,