rs587782609

Orientation

minus

Stabilized

minus

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

Make rs587782609(AAT;AAT)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7676211

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587782609
dbSNP (classic)	rs587782609
ClinGen	rs587782609
ebi	rs587782609
HLI	rs587782609
Exac	rs587782609
Gnomad	rs587782609
Varsome	rs587782609
LitVar	rs587782609
Map	rs587782609
PheGenI	rs587782609
Biobank	rs587782609
1000 genomes	rs587782609
hgdp	rs587782609
ensembl	rs587782609
geneview	rs587782609
scholar	rs587782609
google	rs587782609
pharmgkb	rs587782609
gwascentral	rs587782609
openSNP	rs587782609
23andMe	rs587782609
SNPshot	rs587782609
SNPdbe	rs587782609
MSV3d	rs587782609
GWAS Ctlg	rs587782609

Max Magnitude

7

ClinVar
Risk	rs587782609(AAT;AAT)
Alt	rs587782609(AAT;AAT)
Reference	Rs587782609(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7579530_7579532dupATT
CLNSRC
CLNACC	RCV000131982.2,