rs55832599

Orientation

plus

Stabilized

plus

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

Make rs55832599(A;A)

Reference

GRCh38 38.1/142

Chromosome

17

Position

7673821

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs55832599
dbSNP (classic)	rs55832599
ClinGen	rs55832599
ebi	rs55832599
HLI	rs55832599
Exac	rs55832599
Gnomad	rs55832599
Varsome	rs55832599
LitVar	rs55832599
Map	rs55832599
PheGenI	rs55832599
Biobank	rs55832599
1000 genomes	rs55832599
hgdp	rs55832599
ensembl	rs55832599
geneview	rs55832599
scholar	rs55832599
google	rs55832599
pharmgkb	rs55832599
gwascentral	rs55832599
openSNP	rs55832599
23andMe	rs55832599
SNPshot	rs55832599
SNPdbe	rs55832599
MSV3d	rs55832599
GWAS Ctlg	rs55832599

Max Magnitude

7

ClinVar
Risk	rs55832599(A;A)
Alt	rs55832599(A;A)
Reference	Rs55832599(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000017.10:g.7577139G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000130398.4, RCV000413074.1,