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rs786201057

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201057(C;T)
Make rs786201057(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675995
GeneTP53
is asnp
is mentioned by
dbSNPrs786201057
ebirs786201057
HLIrs786201057
Exacrs786201057
Varsomers786201057
Maprs786201057
PheGenIrs786201057
hapmaprs786201057
1000 genomesrs786201057
hgdprs786201057
ensemblrs786201057
gopubmedrs786201057
geneviewrs786201057
scholarrs786201057
googlers786201057
pharmgkbrs786201057
gwascentralrs786201057
openSNPrs786201057
23andMers786201057
23andMe allrs786201057
SNP Nexus

SNPshotrs786201057
SNPdbers786201057
MSV3drs786201057
GWAS Ctlgrs786201057
Max Magnitude0
ClinVar
Risk rs786201057(A,T;A,T)
Alt rs786201057(A,T;A,T)
Reference rs786201057(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome not specified Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579313G>A; NC_000017.10:g.7579313G>T
CLNSRC
CLNACC RCV000162461.2, RCV000237013.1, RCV000197507.1,