rs587782393

Orientation

minus

Stabilized

minus

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

Make rs587782393(-;-)

Make rs587782393(-;CACACCCCCGCCC)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7675153

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587782393
dbSNP (classic)	rs587782393
ClinGen	rs587782393
ebi	rs587782393
HLI	rs587782393
Exac	rs587782393
Gnomad	rs587782393
Varsome	rs587782393
LitVar	rs587782393
Map	rs587782393
PheGenI	rs587782393
Biobank	rs587782393
1000 genomes	rs587782393
hgdp	rs587782393
ensembl	rs587782393
geneview	rs587782393
scholar	rs587782393
google	rs587782393
pharmgkb	rs587782393
gwascentral	rs587782393
openSNP	rs587782393
23andMe	rs587782393
SNPshot	rs587782393
SNPdbe	rs587782393
MSV3d	rs587782393
GWAS Ctlg	rs587782393

Max Magnitude

0

ClinVar
Risk	rs587782393(-;-)
Alt	rs587782393(-;-)
Reference	Rs587782393(CACACCCCCGCCC;CACACCCCCGCCC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578471_7578483delGGGCGGGGGTGTG
CLNSRC
CLNACC	RCV000131407.2,