rs730882019

Orientation

minus

Stabilized

minus

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

Make rs730882019(-;C)

Make rs730882019(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7675156

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs730882019
dbSNP (classic)	rs730882019
ClinGen	rs730882019
ebi	rs730882019
HLI	rs730882019
Exac	rs730882019
Gnomad	rs730882019
Varsome	rs730882019
LitVar	rs730882019
Map	rs730882019
PheGenI	rs730882019
Biobank	rs730882019
1000 genomes	rs730882019
hgdp	rs730882019
ensembl	rs730882019
geneview	rs730882019
scholar	rs730882019
google	rs730882019
pharmgkb	rs730882019
gwascentral	rs730882019
openSNP	rs730882019
23andMe	rs730882019
SNPshot	rs730882019
SNPdbe	rs730882019
MSV3d	rs730882019
GWAS Ctlg	rs730882019

Max Magnitude

0

ClinVar
Risk	rs730882019(C;C)
Alt	rs730882019(C;C)
Reference	Rs730882019(-;-)
Significance	Pathogenic
Disease	Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578475dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013157.20, RCV000161060.1,