rs786202514

Orientation

minus

Stabilized

minus

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

Make rs786202514(GAGGT;GAGGT)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

7675096

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs786202514
dbSNP (classic)	rs786202514
ClinGen	rs786202514
ebi	rs786202514
HLI	rs786202514
Exac	rs786202514
Gnomad	rs786202514
Varsome	rs786202514
LitVar	rs786202514
Map	rs786202514
PheGenI	rs786202514
Biobank	rs786202514
1000 genomes	rs786202514
hgdp	rs786202514
ensembl	rs786202514
geneview	rs786202514
scholar	rs786202514
google	rs786202514
pharmgkb	rs786202514
gwascentral	rs786202514
openSNP	rs786202514
23andMe	rs786202514
SNPshot	rs786202514
SNPdbe	rs786202514
MSV3d	rs786202514
GWAS Ctlg	rs786202514

Max Magnitude

7

ClinVar
Risk	rs786202514(GAGGT;GAGGT)
Alt	rs786202514(GAGGT;GAGGT)
Reference	Rs786202514(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578415_7578419dupACCTC
CLNSRC
CLNACC	RCV000165358.1,