rs876658982

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs876658982(A;A)

Make rs876658982(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7669691

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876658982
dbSNP (classic)	rs876658982
ClinGen	rs876658982
ebi	rs876658982
HLI	rs876658982
Exac	rs876658982
Gnomad	rs876658982
Varsome	rs876658982
LitVar	rs876658982
Map	rs876658982
PheGenI	rs876658982
Biobank	rs876658982
1000 genomes	rs876658982
hgdp	rs876658982
ensembl	rs876658982
geneview	rs876658982
scholar	rs876658982
google	rs876658982
pharmgkb	rs876658982
gwascentral	rs876658982
openSNP	rs876658982
23andMe	rs876658982
SNPshot	rs876658982
SNPdbe	rs876658982
MSV3d	rs876658982
GWAS Ctlg	rs876658982

Max Magnitude

0

ClinVar
Risk	rs876658982(A;A)
Alt	rs876658982(A;A)
Reference	Rs876658982(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed	1
HGVS	NC_000017.10:g.7573009C>T
CLNSRC
CLNACC	RCV000222547.2, RCV000466199.1,