rs730882006

Orientation

minus

Stabilized

minus

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

Make rs730882006(C;C)

Make rs730882006(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7674235

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs730882006
dbSNP (classic)	rs730882006
ClinGen	rs730882006
ebi	rs730882006
HLI	rs730882006
Exac	rs730882006
Gnomad	rs730882006
Varsome	rs730882006
LitVar	rs730882006
Map	rs730882006
PheGenI	rs730882006
Biobank	rs730882006
1000 genomes	rs730882006
hgdp	rs730882006
ensembl	rs730882006
geneview	rs730882006
scholar	rs730882006
google	rs730882006
pharmgkb	rs730882006
gwascentral	rs730882006
openSNP	rs730882006
23andMe	rs730882006
SNPshot	rs730882006
SNPdbe	rs730882006
MSV3d	rs730882006
GWAS Ctlg	rs730882006

Max Magnitude

0

ClinVar
Risk	rs730882006(C;C)
Alt	rs730882006(C;C)
Reference	Rs730882006(T;T)
Significance	Probable-Pathogenic
Disease	not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	not specified Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577553A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000161035.1, RCV000222280.1,