rs876660548

Orientation

minus

Stabilized

minus

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

Make rs876660548(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7676096

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876660548
dbSNP (classic)	rs876660548
ClinGen	rs876660548
ebi	rs876660548
HLI	rs876660548
Exac	rs876660548
Gnomad	rs876660548
Varsome	rs876660548
LitVar	rs876660548
Map	rs876660548
PheGenI	rs876660548
Biobank	rs876660548
1000 genomes	rs876660548
hgdp	rs876660548
ensembl	rs876660548
geneview	rs876660548
scholar	rs876660548
google	rs876660548
pharmgkb	rs876660548
gwascentral	rs876660548
openSNP	rs876660548
23andMe	rs876660548
SNPshot	rs876660548
SNPdbe	rs876660548
MSV3d	rs876660548
GWAS Ctlg	rs876660548

Max Magnitude

7

ClinVar
Risk	rs876660548(A;A)
Alt	rs876660548(A;A)
Reference	Rs876660548(G;G)
Significance	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.7579414C>T
CLNSRC
CLNACC	RCV000220815.2, RCV000233967.1,