rs587782650

Orientation

minus

Stabilized

minus

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

Make rs587782650(GT;GT)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7676232

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587782650
dbSNP (classic)	rs587782650
ClinGen	rs587782650
ebi	rs587782650
HLI	rs587782650
Exac	rs587782650
Gnomad	rs587782650
Varsome	rs587782650
LitVar	rs587782650
Map	rs587782650
PheGenI	rs587782650
Biobank	rs587782650
1000 genomes	rs587782650
hgdp	rs587782650
ensembl	rs587782650
geneview	rs587782650
scholar	rs587782650
google	rs587782650
pharmgkb	rs587782650
gwascentral	rs587782650
openSNP	rs587782650
23andMe	rs587782650
SNPshot	rs587782650
SNPdbe	rs587782650
MSV3d	rs587782650
GWAS Ctlg	rs587782650

Max Magnitude

7

ClinVar
Risk	rs587782650(GT;GT)
Alt	rs587782650(GT;GT)
Reference	Rs587782650(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7579550delGinsAC
CLNSRC
CLNACC	RCV000132061.2,