rs28934571

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0
(G;G)	0	common in complete genomics

Make rs28934571(G;T)

Make rs28934571(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7674216

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs28934571
dbSNP (classic)	rs28934571
ClinGen	rs28934571
ebi	rs28934571
HLI	rs28934571
Exac	rs28934571
Gnomad	rs28934571
Varsome	rs28934571
LitVar	rs28934571
Map	rs28934571
PheGenI	rs28934571
Biobank	rs28934571
1000 genomes	rs28934571
hgdp	rs28934571
ensembl	rs28934571
geneview	rs28934571
scholar	rs28934571
google	rs28934571
pharmgkb	rs28934571
gwascentral	rs28934571
openSNP	rs28934571
23andMe	rs28934571
SNPshot	rs28934571
SNPdbe	rs28934571
MSV3d	rs28934571
GWAS Ctlg	rs28934571

Max Magnitude

0

OMIM	191170
Desc	HEPATOCELLULAR CARCINOMA
Variant	0006
Related	also

ClinVar
Risk	Rs28934571(C;C) rs28934571(T;T)
Alt	Rs28934571(C;C) rs28934571(T;T)
Reference	Rs28934571(G;G)
Significance	Pathogenic
Disease	Hepatocellular carcinoma Carcinoma of cervix Li-Fraumeni syndrome
Variation	info
Gene	TP53
CLNDBN	Hepatocellular carcinoma Carcinoma of cervix Li-Fraumeni syndrome
Reversed	1
HGVS	NC_000017.10:g.7577534C>A; NC_000017.10:g.7577534C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013145.4, RCV000013146.4, RCV000464372.1, RCV000465003.1,