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rs1060501195

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501195(C;C)
Make rs1060501195(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7676056
GeneTP53
is asnp
is mentioned by
dbSNPrs1060501195
dbSNP (old)rs1060501195
ClinGenrs1060501195
ebirs1060501195
HLIrs1060501195
Exacrs1060501195
Gnomadrs1060501195
Varsomers1060501195
Maprs1060501195
PheGenIrs1060501195
Biobankrs1060501195
1000 genomesrs1060501195
hgdprs1060501195
ensemblrs1060501195
gopubmedrs1060501195
geneviewrs1060501195
scholarrs1060501195
googlers1060501195
pharmgkbrs1060501195
gwascentralrs1060501195
openSNPrs1060501195
23andMers1060501195
23andMe allrs1060501195
SNPshotrs1060501195
SNPdbers1060501195
MSV3drs1060501195
GWAS Ctlgrs1060501195
Max Magnitude0
ClinVar
Risk rs1060501195(C;C)
Alt rs1060501195(C;C)
Reference Rs1060501195(G;G)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579374C>G; NC_000017.10:g.7579374C>T
CLNSRC
CLNACC RCV000475325.1, RCV000492606.1, RCV000492331.1,