rs876659384

Orientation

minus

Stabilized

minus

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

Make rs876659384(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7673552

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876659384
dbSNP (classic)	rs876659384
ClinGen	rs876659384
ebi	rs876659384
HLI	rs876659384
Exac	rs876659384
Gnomad	rs876659384
Varsome	rs876659384
LitVar	rs876659384
Map	rs876659384
PheGenI	rs876659384
Biobank	rs876659384
1000 genomes	rs876659384
hgdp	rs876659384
ensembl	rs876659384
geneview	rs876659384
scholar	rs876659384
google	rs876659384
pharmgkb	rs876659384
gwascentral	rs876659384
openSNP	rs876659384
23andMe	rs876659384
SNPshot	rs876659384
SNPdbe	rs876659384
MSV3d	rs876659384
GWAS Ctlg	rs876659384

Max Magnitude

7

ClinVar
Risk	rs876659384(T;T)
Alt	rs876659384(T;T)
Reference	Rs876659384(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7576870C>A
CLNSRC
CLNACC	RCV000218971.1,