rs876660726

Orientation

minus

Stabilized

minus

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

Make rs876660726(-;-)

Make rs876660726(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7673718

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876660726
dbSNP (classic)	rs876660726
ClinGen	rs876660726
ebi	rs876660726
HLI	rs876660726
Exac	rs876660726
Gnomad	rs876660726
Varsome	rs876660726
LitVar	rs876660726
Map	rs876660726
PheGenI	rs876660726
Biobank	rs876660726
1000 genomes	rs876660726
hgdp	rs876660726
ensembl	rs876660726
geneview	rs876660726
scholar	rs876660726
google	rs876660726
pharmgkb	rs876660726
gwascentral	rs876660726
openSNP	rs876660726
23andMe	rs876660726
SNPshot	rs876660726
SNPdbe	rs876660726
MSV3d	rs876660726
GWAS Ctlg	rs876660726

Max Magnitude

0

ClinVar
Risk	rs876660726(-;-)
Alt	rs876660726(-;-)
Reference	Rs876660726(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577036delG
CLNSRC
CLNACC	RCV000219373.2,