rs587780066

Orientation

minus

Stabilized

minus

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

Make rs587780066(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7676041

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587780066
dbSNP (classic)	rs587780066
ClinGen	rs587780066
ebi	rs587780066
HLI	rs587780066
Exac	rs587780066
Gnomad	rs587780066
Varsome	rs587780066
LitVar	rs587780066
Map	rs587780066
PheGenI	rs587780066
Biobank	rs587780066
1000 genomes	rs587780066
hgdp	rs587780066
ensembl	rs587780066
geneview	rs587780066
scholar	rs587780066
google	rs587780066
pharmgkb	rs587780066
gwascentral	rs587780066
openSNP	rs587780066
23andMe	rs587780066
SNPshot	rs587780066
SNPdbe	rs587780066
MSV3d	rs587780066
GWAS Ctlg	rs587780066

Max Magnitude

7

ClinVar
Risk	rs587780066(-;-)
Alt	rs587780066(-;-)
Reference	Rs587780066(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7579359delG
CLNSRC
CLNACC	RCV000115718.2,