rs587781564

Orientation

minus

Stabilized

minus

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

Make rs587781564(AGAGACCGGCG;CA)

Make rs587781564(CA;CA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7673772

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587781564
dbSNP (classic)	rs587781564
ClinGen	rs587781564
ebi	rs587781564
HLI	rs587781564
Exac	rs587781564
Gnomad	rs587781564
Varsome	rs587781564
LitVar	rs587781564
Map	rs587781564
PheGenI	rs587781564
Biobank	rs587781564
1000 genomes	rs587781564
hgdp	rs587781564
ensembl	rs587781564
geneview	rs587781564
scholar	rs587781564
google	rs587781564
pharmgkb	rs587781564
gwascentral	rs587781564
openSNP	rs587781564
23andMe	rs587781564
SNPshot	rs587781564
SNPdbe	rs587781564
MSV3d	rs587781564
GWAS Ctlg	rs587781564

Max Magnitude

0

ClinVar
Risk	rs587781564(CA;CA)
Alt	rs587781564(CA;CA)
Reference	Rs587781564(AGAGACCGGCG;AGAGACCGGCG)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577090_7577100delCGCCGGTCTCTinsTG
CLNSRC
CLNACC	RCV000129588.2,