rs587780074

Orientation

minus

Stabilized

minus

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

Make rs587780074(G;G)

Make rs587780074(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

7674226

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs587780074
dbSNP (classic)	rs587780074
ClinGen	rs587780074
ebi	rs587780074
HLI	rs587780074
Exac	rs587780074
Gnomad	rs587780074
Varsome	rs587780074
LitVar	rs587780074
Map	rs587780074
PheGenI	rs587780074
Biobank	rs587780074
1000 genomes	rs587780074
hgdp	rs587780074
ensembl	rs587780074
geneview	rs587780074
scholar	rs587780074
google	rs587780074
pharmgkb	rs587780074
gwascentral	rs587780074
openSNP	rs587780074
23andMe	rs587780074
SNPshot	rs587780074
SNPdbe	rs587780074
MSV3d	rs587780074
GWAS Ctlg	rs587780074

Max Magnitude

7

ClinVar
Risk	rs587780074(G;G)
Alt	rs587780074(G;G)
Reference	Rs587780074(T;T)
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.7577544A>C; NC_000017.10:g.7577544A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000115734.2, RCV000492075.1,