rs878854071

Orientation

minus

Stabilized

minus

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

Make rs878854071(-;-)

Make rs878854071(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

7674869

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs878854071
dbSNP (classic)	rs878854071
ClinGen	rs878854071
ebi	rs878854071
HLI	rs878854071
Exac	rs878854071
Gnomad	rs878854071
Varsome	rs878854071
LitVar	rs878854071
Map	rs878854071
PheGenI	rs878854071
Biobank	rs878854071
1000 genomes	rs878854071
hgdp	rs878854071
ensembl	rs878854071
geneview	rs878854071
scholar	rs878854071
google	rs878854071
pharmgkb	rs878854071
gwascentral	rs878854071
openSNP	rs878854071
23andMe	rs878854071
SNPshot	rs878854071
SNPdbe	rs878854071
MSV3d	rs878854071
GWAS Ctlg	rs878854071

Max Magnitude

0

ClinVar
Risk	rs878854071(-;-)
Alt	rs878854071(-;-)
Reference	Rs878854071(A;A)
Significance	Pathogenic
Disease	Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7578187delT
CLNSRC
CLNACC	RCV000234225.1, RCV000492096.1,