rs876658144

Orientation

minus

Stabilized

minus

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

Make rs876658144(-;-)

Make rs876658144(-;CTATGAGCC)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7674866

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs876658144
dbSNP (classic)	rs876658144
ClinGen	rs876658144
ebi	rs876658144
HLI	rs876658144
Exac	rs876658144
Gnomad	rs876658144
Varsome	rs876658144
LitVar	rs876658144
Map	rs876658144
PheGenI	rs876658144
Biobank	rs876658144
1000 genomes	rs876658144
hgdp	rs876658144
ensembl	rs876658144
geneview	rs876658144
scholar	rs876658144
google	rs876658144
pharmgkb	rs876658144
gwascentral	rs876658144
openSNP	rs876658144
23andMe	rs876658144
SNPshot	rs876658144
SNPdbe	rs876658144
MSV3d	rs876658144
GWAS Ctlg	rs876658144

Max Magnitude

0

ClinVar
Risk	rs876658144(-;-)
Alt	rs876658144(-;-)
Reference	Rs876658144(CTATGAGCC;CTATGAGCC)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578184_7578192delGGCTCATAG
CLNSRC
CLNACC	RCV000222764.1,