rs786202315

Orientation

minus

Stabilized

minus

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

Make rs786202315(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

7674865

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs786202315
dbSNP (classic)	rs786202315
ClinGen	rs786202315
ebi	rs786202315
HLI	rs786202315
Exac	rs786202315
Gnomad	rs786202315
Varsome	rs786202315
LitVar	rs786202315
Map	rs786202315
PheGenI	rs786202315
Biobank	rs786202315
1000 genomes	rs786202315
hgdp	rs786202315
ensembl	rs786202315
geneview	rs786202315
scholar	rs786202315
google	rs786202315
pharmgkb	rs786202315
gwascentral	rs786202315
openSNP	rs786202315
23andMe	rs786202315
SNPshot	rs786202315
SNPdbe	rs786202315
MSV3d	rs786202315
GWAS Ctlg	rs786202315

Max Magnitude

7

ClinVar
Risk	rs786202315(-;-)
Alt	rs786202315(-;-)
Reference	Rs786202315(GGTGCCCTATGAGCCG;GGTGCCCTATGAGCCG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578183_7578198del16
CLNSRC
CLNACC	RCV000165061.1,