rs121912653

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;T)	7	Li-Fraumeni Syndrome (predicted)
(T;T)	0	common in clinvar

Make rs121912653(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7674208

Gene

TP53

is a	snp
is	mentioned by
dbSNP	rs121912653
dbSNP (classic)	rs121912653
ClinGen	rs121912653
ebi	rs121912653
HLI	rs121912653
Exac	rs121912653
Gnomad	rs121912653
Varsome	rs121912653
LitVar	rs121912653
Map	rs121912653
PheGenI	rs121912653
Biobank	rs121912653
1000 genomes	rs121912653
hgdp	rs121912653
ensembl	rs121912653
geneview	rs121912653
scholar	rs121912653
google	rs121912653
pharmgkb	rs121912653
gwascentral	rs121912653
openSNP	rs121912653
23andMe	rs121912653
SNPshot	rs121912653
SNPdbe	rs121912653
MSV3d	rs121912653
GWAS Ctlg	rs121912653

Max Magnitude

7

OMIM	191170
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121912653(C;C)
Alt	rs121912653(C;C)
Reference	Rs121912653(T;T)
Significance	Pathogenic
Disease	Li-Fraumeni syndrome 1
Variation	info
Gene	TP53
CLNDBN	Li-Fraumeni syndrome 1
Reversed	1
HGVS	NC_000017.10:g.7577526A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013143.20,