rs876659215

Orientation

minus

Stabilized

minus

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

Make rs876659215(-;-)

Make rs876659215(-;CCGCCCGGCACCC)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7675146

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876659215
dbSNP (classic)	rs876659215
ClinGen	rs876659215
ebi	rs876659215
HLI	rs876659215
Exac	rs876659215
Gnomad	rs876659215
Varsome	rs876659215
LitVar	rs876659215
Map	rs876659215
PheGenI	rs876659215
Biobank	rs876659215
1000 genomes	rs876659215
hgdp	rs876659215
ensembl	rs876659215
geneview	rs876659215
scholar	rs876659215
google	rs876659215
pharmgkb	rs876659215
gwascentral	rs876659215
openSNP	rs876659215
23andMe	rs876659215
SNPshot	rs876659215
SNPdbe	rs876659215
MSV3d	rs876659215
GWAS Ctlg	rs876659215

Max Magnitude

0

ClinVar
Risk	rs876659215(-;-)
Alt	rs876659215(-;-)
Reference	Rs876659215(CCGCCCGGCACCC;CCGCCCGGCACCC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578464_7578476delGGGTGCCGGGCGG
CLNSRC
CLNACC	RCV000220919.1,