rs587782272

Orientation

minus

Stabilized

minus

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

Make rs587782272(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7670716

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587782272
dbSNP (classic)	rs587782272
ClinGen	rs587782272
ebi	rs587782272
HLI	rs587782272
Exac	rs587782272
Gnomad	rs587782272
Varsome	rs587782272
LitVar	rs587782272
Map	rs587782272
PheGenI	rs587782272
Biobank	rs587782272
1000 genomes	rs587782272
hgdp	rs587782272
ensembl	rs587782272
geneview	rs587782272
scholar	rs587782272
google	rs587782272
pharmgkb	rs587782272
gwascentral	rs587782272
openSNP	rs587782272
23andMe	rs587782272
SNPshot	rs587782272
SNPdbe	rs587782272
MSV3d	rs587782272
GWAS Ctlg	rs587782272

Max Magnitude

7

ClinVar
Risk	rs587782272(A;A) rs587782272(C;C)
Alt	rs587782272(A;A) rs587782272(C;C)
Reference	Rs587782272(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.7574034C>G; NC_000017.10:g.7574034C>T
CLNSRC
CLNACC	RCV000221716.1, RCV000131124.2,