rs1064793881

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

7673784

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1064793881
dbSNP (classic)	rs1064793881
ClinGen	rs1064793881
ebi	rs1064793881
HLI	rs1064793881
Exac	rs1064793881
Gnomad	rs1064793881
Varsome	rs1064793881
LitVar	rs1064793881
Map	rs1064793881
PheGenI	rs1064793881
Biobank	rs1064793881
1000 genomes	rs1064793881
hgdp	rs1064793881
ensembl	rs1064793881
geneview	rs1064793881
scholar	rs1064793881
google	rs1064793881
pharmgkb	rs1064793881
gwascentral	rs1064793881
openSNP	rs1064793881
23andMe	rs1064793881
SNPshot	rs1064793881
SNPdbe	rs1064793881
MSV3d	rs1064793881
GWAS Ctlg	rs1064793881

Max Magnitude

0

ClinVar
Risk	rs1064793881(A;A)
Alt	rs1064793881(A;A)
Reference	Rs1064793881(G;G)
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.7577102C>T
CLNSRC
CLNACC	RCV000484876.1, RCV000492354.1,