rs730882007

Orientation

minus

Stabilized

minus

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

Make rs730882007(A;C)

Make rs730882007(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7674212

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs730882007
dbSNP (classic)	rs730882007
ClinGen	rs730882007
ebi	rs730882007
HLI	rs730882007
Exac	rs730882007
Gnomad	rs730882007
Varsome	rs730882007
LitVar	rs730882007
Map	rs730882007
PheGenI	rs730882007
Biobank	rs730882007
1000 genomes	rs730882007
hgdp	rs730882007
ensembl	rs730882007
geneview	rs730882007
scholar	rs730882007
google	rs730882007
pharmgkb	rs730882007
gwascentral	rs730882007
openSNP	rs730882007
23andMe	rs730882007
SNPshot	rs730882007
SNPdbe	rs730882007
MSV3d	rs730882007
GWAS Ctlg	rs730882007

Max Magnitude

0

ClinVar
Risk	rs730882007(C;C)
Alt	rs730882007(C;C)
Reference	Rs730882007(A;A)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577530T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000161037.2, RCV000492548.1,