rs1057522275

Orientation

minus

Stabilized

minus

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

Make rs1057522275(C;G)

Make rs1057522275(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7674246

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs1057522275
dbSNP (classic)	rs1057522275
ClinGen	rs1057522275
ebi	rs1057522275
HLI	rs1057522275
Exac	rs1057522275
Gnomad	rs1057522275
Varsome	rs1057522275
LitVar	rs1057522275
Map	rs1057522275
PheGenI	rs1057522275
Biobank	rs1057522275
1000 genomes	rs1057522275
hgdp	rs1057522275
ensembl	rs1057522275
geneview	rs1057522275
scholar	rs1057522275
google	rs1057522275
pharmgkb	rs1057522275
gwascentral	rs1057522275
openSNP	rs1057522275
23andMe	rs1057522275
SNPshot	rs1057522275
SNPdbe	rs1057522275
MSV3d	rs1057522275
GWAS Ctlg	rs1057522275

Max Magnitude

0

ClinVar
Risk	rs1057522275(G;G)
Alt	rs1057522275(G;G)
Reference	Rs1057522275(C;C)
Significance	Probable-Pathogenic
Disease	not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	TP53
CLNDBN	not specified Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.7577564G>C
CLNSRC
CLNACC	RCV000431317.1, RCV000492173.1,