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

rs876659802

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659802(C;T)
Make rs876659802(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7673787
GeneTP53
is asnp
is mentioned by
dbSNPrs876659802
dbSNP (old)rs876659802
ClinGenrs876659802
ebirs876659802
HLIrs876659802
Exacrs876659802
Gnomadrs876659802
Varsomers876659802
Maprs876659802
PheGenIrs876659802
Biobankrs876659802
1000 genomesrs876659802
hgdprs876659802
ensemblrs876659802
gopubmedrs876659802
geneviewrs876659802
scholarrs876659802
googlers876659802
pharmgkbrs876659802
gwascentralrs876659802
openSNPrs876659802
23andMers876659802
23andMe allrs876659802
SNP Nexus

SNPshotrs876659802
SNPdbers876659802
MSV3drs876659802
GWAS Ctlgrs876659802
Max Magnitude0
ClinVar
Risk rs876659802(A;A) rs876659802(G;G) rs876659802(T;T)
Alt rs876659802(A;A) rs876659802(G;G) rs876659802(T;T)
Reference Rs876659802(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Colorectal Neoplasms Malignant neoplasm of body of uterus Neoplasm of brain Neoplasm of breast Squamous cell carcinoma of the skin Oesophageal carcinoma Squamous cell carcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Malignant melanoma of skin Multiple myeloma
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Colorectal Neoplasms Malignant neoplasm of body of uterus Neoplasm of brain Neoplasm of breast Squamous cell carcinoma of the skin Oesophageal carcinoma Squamous cell carcinoma of lung Pancreatic adenocarcinoma Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Malignant melanoma of skin Multiple myeloma
Reversed 1
HGVS NC_000017.10:g.7577105G>A; NC_000017.10:g.7577105G>C; NC_000017.10:g.7577105G>T
CLNSRC
CLNACC RCV000214784.1, RCV000417969.1, RCV000419043.1, RCV000421915.1, RCV000423023.1, RCV000424153.1, RCV000428205.1, RCV000429345.1, RCV000430442.1, RCV000433311.1, RCV000434963.1, RCV000439555.1, RCV000440687.1, RCV000443824.1, RCV000420956.1, RCV000423863.1, RCV000424036.1, RCV000425930.1, RCV000426582.1, RCV000431305.1, RCV000431661.1, RCV000431945.1, RCV000432244.1, RCV000441126.1, RCV000443337.1, RCV000443990.1, RCV000444083.1, RCV000417607.1, RCV000420265.1, RCV000422133.1, RCV000424797.1, RCV000426301.1, RCV000427682.1, RCV000428293.1, RCV000433513.1, RCV000433712.1, RCV000435517.1, RCV000437485.1, RCV000443564.1, RCV000444453.1,