rs587781433

Orientation

minus

Stabilized

minus

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

Make rs587781433(A;G)

Make rs587781433(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7674197

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587781433
dbSNP (classic)	rs587781433
ClinGen	rs587781433
ebi	rs587781433
HLI	rs587781433
Exac	rs587781433
Gnomad	rs587781433
Varsome	rs587781433
LitVar	rs587781433
Map	rs587781433
PheGenI	rs587781433
Biobank	rs587781433
1000 genomes	rs587781433
hgdp	rs587781433
ensembl	rs587781433
geneview	rs587781433
scholar	rs587781433
google	rs587781433
pharmgkb	rs587781433
gwascentral	rs587781433
openSNP	rs587781433
23andMe	rs587781433
SNPshot	rs587781433
SNPdbe	rs587781433
MSV3d	rs587781433
GWAS Ctlg	rs587781433

Max Magnitude

0

ClinVar
Risk	rs587781433(G;G)
Alt	rs587781433(G;G)
Reference	Rs587781433(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Reversed	1
HGVS	NC_000017.10:g.7577515T>C
CLNSRC
CLNACC	RCV000129326.2, RCV000172827.1,