rs763098116

Orientation

plus

Stabilized

plus

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

Make rs763098116(C;T)

Make rs763098116(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7673790

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs763098116
dbSNP (classic)	rs763098116
ClinGen	rs763098116
ebi	rs763098116
HLI	rs763098116
Exac	rs763098116
Gnomad	rs763098116
Varsome	rs763098116
LitVar	rs763098116
Map	rs763098116
PheGenI	rs763098116
Biobank	rs763098116
1000 genomes	rs763098116
hgdp	rs763098116
ensembl	rs763098116
geneview	rs763098116
scholar	rs763098116
google	rs763098116
pharmgkb	rs763098116
gwascentral	rs763098116
openSNP	rs763098116
23andMe	rs763098116
SNPshot	rs763098116
SNPdbe	rs763098116
MSV3d	rs763098116
GWAS Ctlg	rs763098116

Max Magnitude

0

ClinVar
Risk	rs763098116(A;A) rs763098116(T;T)
Alt	rs763098116(A;A) rs763098116(T;T)
Reference	Rs763098116(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Li-Fraumeni syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome not provided Li-Fraumeni syndrome
Reversed	0
HGVS	NC_000017.10:g.7577108C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000165199.1, RCV000254809.1, RCV000456858.1,