rs730882016

Orientation

minus

Stabilized

minus

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

Make rs730882016(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7674271

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs730882016
dbSNP (classic)	rs730882016
ClinGen	rs730882016
ebi	rs730882016
HLI	rs730882016
Exac	rs730882016
Gnomad	rs730882016
Varsome	rs730882016
LitVar	rs730882016
Map	rs730882016
PheGenI	rs730882016
Biobank	rs730882016
1000 genomes	rs730882016
hgdp	rs730882016
ensembl	rs730882016
geneview	rs730882016
scholar	rs730882016
google	rs730882016
pharmgkb	rs730882016
gwascentral	rs730882016
openSNP	rs730882016
23andMe	rs730882016
SNPshot	rs730882016
SNPdbe	rs730882016
MSV3d	rs730882016
GWAS Ctlg	rs730882016

Max Magnitude

7

ClinVar
Risk	rs730882016(-;-)
Alt	rs730882016(-;-)
Reference	Rs730882016(TGTACCAC;TGTACCAC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577589_7577596delGTGGTACA
CLNSRC
CLNACC	RCV000161057.1,