rs59758982

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CCCCAGCCCTCCAGGT;CCCCAGCCCTCCAGGT)	0	common in clinvar
(TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCC)	0	common in clinvar

Make rs59758982(-;-)

Make rs59758982(-;T)

Make rs59758982(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7676351

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs59758982
dbSNP (classic)	rs59758982
ClinGen	rs59758982
ebi	rs59758982
HLI	rs59758982
Exac	rs59758982
Gnomad	rs59758982
Varsome	rs59758982
LitVar	rs59758982
Map	rs59758982
PheGenI	rs59758982
Biobank	rs59758982
1000 genomes	rs59758982
hgdp	rs59758982
ensembl	rs59758982
geneview	rs59758982
scholar	rs59758982
google	rs59758982
pharmgkb	rs59758982
gwascentral	rs59758982
openSNP	rs59758982
23andMe	rs59758982
SNPshot	rs59758982
SNPdbe	rs59758982
MSV3d	rs59758982
GWAS Ctlg	rs59758982

Max Magnitude

0

[PMID 19471604] Lack of association between p53 gene polymorphisms and primary open angle glaucoma in the Japanese population

ClinVar
Risk	rs59758982(-;-) rs59758982(CAGGTCCCCAGCCCTC;CAGGTCCCCAGCCCTC) Rs59758982(CCCCAGCCCTCCAGGT;CCCCAGCCCTCCAGGT)
Alt	rs59758982(-;-) rs59758982(CAGGTCCCCAGCCCTC;CAGGTCCCCAGCCCTC) Rs59758982(CCCCAGCCCTCCAGGT;CCCCAGCCCTCCAGGT)
Reference	Rs59758982(TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCC)
Significance	Non-pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.7579669_7579684del16
CLNSRC
CLNACC	RCV000161045.1,