rs1060501194

Orientation

minus

Stabilized

minus

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

Make rs1060501194(-;-)

Make rs1060501194(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7673830

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1060501194
dbSNP (classic)	rs1060501194
ClinGen	rs1060501194
ebi	rs1060501194
HLI	rs1060501194
Exac	rs1060501194
Gnomad	rs1060501194
Varsome	rs1060501194
LitVar	rs1060501194
Map	rs1060501194
PheGenI	rs1060501194
Biobank	rs1060501194
1000 genomes	rs1060501194
hgdp	rs1060501194
ensembl	rs1060501194
geneview	rs1060501194
scholar	rs1060501194
google	rs1060501194
pharmgkb	rs1060501194
gwascentral	rs1060501194
openSNP	rs1060501194
23andMe	rs1060501194
SNPshot	rs1060501194
SNPdbe	rs1060501194
MSV3d	rs1060501194
GWAS Ctlg	rs1060501194

Max Magnitude

0

ClinVar
Risk	rs1060501194(-;-)
Alt	rs1060501194(-;-)
Reference	Rs1060501194(C;C)
Significance	Pathogenic
Disease	Li-Fraumeni syndrome
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni syndrome
Reversed	1
HGVS	NC_000017.10:g.7577148delG
CLNSRC
CLNACC	RCV000472594.1,