rs397516439

Orientation

minus

Stabilized

minus

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

Make rs397516439(A;G)

Make rs397516439(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7673610

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs397516439
dbSNP (classic)	rs397516439
ClinGen	rs397516439
ebi	rs397516439
HLI	rs397516439
Exac	rs397516439
Gnomad	rs397516439
Varsome	rs397516439
LitVar	rs397516439
Map	rs397516439
PheGenI	rs397516439
Biobank	rs397516439
1000 genomes	rs397516439
hgdp	rs397516439
ensembl	rs397516439
geneview	rs397516439
scholar	rs397516439
google	rs397516439
pharmgkb	rs397516439
gwascentral	rs397516439
openSNP	rs397516439
23andMe	rs397516439
SNPshot	rs397516439
SNPdbe	rs397516439
MSV3d	rs397516439
GWAS Ctlg	rs397516439

Max Magnitude

0

ClinVar
Risk	rs397516439(G;G)
Alt	rs397516439(G;G)
Reference	Rs397516439(A;A)
Significance	Pathogenic
Disease	Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.7576928T>C
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000036537.2, RCV000132190.2, RCV000483617.1,