rs876658468

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	7	Li-Fraumeni Syndrome (predicted)

Make rs876658468(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7674954

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876658468
dbSNP (classic)	rs876658468
ClinGen	rs876658468
ebi	rs876658468
HLI	rs876658468
Exac	rs876658468
Gnomad	rs876658468
Varsome	rs876658468
LitVar	rs876658468
Map	rs876658468
PheGenI	rs876658468
Biobank	rs876658468
1000 genomes	rs876658468
hgdp	rs876658468
ensembl	rs876658468
geneview	rs876658468
scholar	rs876658468
google	rs876658468
pharmgkb	rs876658468
gwascentral	rs876658468
openSNP	rs876658468
23andMe	rs876658468
SNPshot	rs876658468
SNPdbe	rs876658468
MSV3d	rs876658468
GWAS Ctlg	rs876658468

Max Magnitude

7

ClinVar
Risk	rs876658468(A;A) rs876658468(G;G) rs876658468(T;T)
Alt	rs876658468(A;A) rs876658468(G;G) rs876658468(T;T)
Reference	Rs876658468(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Adenocarcinoma of stomach Papillary renal cell carcinoma Hepatocellular carcinoma Pancreatic adenocarcinoma Brainstem glioma Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Colorectal Neoplasms Neoplasm of brain Adenocarcinoma of prostate Adenocarcinoma of lung Squamous cell carcinoma of lung Uterine Carcinosarcoma Acute myeloid leukemia Oesophageal carcinoma Neoplasm of breast Small cell lung cancer Transitional cell carcinoma of the bladder Ovarian Serous Cystadenocarcinoma
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome not provided Adenocarcinoma of stomach Papillary renal cell carcinoma, sporadic Hepatocellular carcinoma Pancreatic adenocarcinoma Brainstem glioma Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Colorectal Neoplasms Neoplasm of brain Adenocarcinoma of prostate Adenocarcinoma of lung Squamous cell carcinoma of lung Uterine Carcinosarcoma Acute myeloid leukemia Oesophageal carcinoma Neoplasm of breast Small cell lung cancer Transitional cell carcinoma of the bladder Ovarian Serous Cystadenocarcinoma
Reversed	1
HGVS	NC_000017.10:g.7578272G>A; NC_000017.10:g.7578272G>C; NC_000017.10:g.7578272G>T
CLNSRC
CLNACC	RCV000221478.1, RCV000412758.1, RCV000418749.1, RCV000419469.1, RCV000419839.1, RCV000421204.1, RCV000423524.1, RCV000424900.1, RCV000425998.1, RCV000426264.1, RCV000429902.1, RCV000430089.1, RCV000431464.1, RCV000432551.1, RCV000434647.1, RCV000436284.1, RCV000437380.1, RCV000440111.1, RCV000441207.1, RCV000441502.1, RCV000444740.1, RCV000445008.1, RCV000418378.1, RCV000419005.1, RCV000419924.1, RCV000421156.1, RCV000423999.1, RCV000425273.1, RCV000425552.1, RCV000425919.1, RCV000429967.1, RCV000430614.1, RCV000431849.1, RCV000432462.1, RCV000434704.1, RCV000436250.1, RCV000436620.1, RCV000438391.1, RCV000440641.1, RCV000441340.1, RCV000442175.1, RCV000444718.1, RCV000419544.1, RCV000420192.1, RCV000420894.1, RCV000421458.1, RCV000422179.1, RCV000422815.1, RCV000426753.1, RCV000427057.1, RCV000428079.1, RCV000430888.1, RCV000432133.1, RCV000432878.1, RCV000433595.1, RCV000437420.1, RCV000437710.1, RCV000438671.1, RCV000439335.1, RCV000441629.1, RCV000441851.1, RCV000444677.1,