rs863223300

Orientation

minus

Stabilized

minus

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

Make rs863223300(-;-)

Make rs863223300(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

7675080

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs863223300
dbSNP (classic)	rs863223300
ClinGen	rs863223300
ebi	rs863223300
HLI	rs863223300
Exac	rs863223300
Gnomad	rs863223300
Varsome	rs863223300
LitVar	rs863223300
Map	rs863223300
PheGenI	rs863223300
Biobank	rs863223300
1000 genomes	rs863223300
hgdp	rs863223300
ensembl	rs863223300
geneview	rs863223300
scholar	rs863223300
google	rs863223300
pharmgkb	rs863223300
gwascentral	rs863223300
openSNP	rs863223300
23andMe	rs863223300
SNPshot	rs863223300
SNPdbe	rs863223300
MSV3d	rs863223300
GWAS Ctlg	rs863223300

Max Magnitude

0

ClinVar
Risk	rs863223300(-;-)
Alt	rs863223300(-;-)
Reference	Rs863223300(C;C)
Significance	Pathogenic
Disease	Li-Fraumeni syndrome 1 Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni syndrome 1 Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578398delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013176.23, RCV000215848.1,