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rs1060501194

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501194(-;-)
Make rs1060501194(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673830
GeneTP53
is asnp
is mentioned by
dbSNPrs1060501194
dbSNP (old)rs1060501194
ClinGenrs1060501194
ebirs1060501194
HLIrs1060501194
Exacrs1060501194
Gnomadrs1060501194
Varsomers1060501194
Maprs1060501194
PheGenIrs1060501194
Biobankrs1060501194
1000 genomesrs1060501194
hgdprs1060501194
ensemblrs1060501194
gopubmedrs1060501194
geneviewrs1060501194
scholarrs1060501194
googlers1060501194
pharmgkbrs1060501194
gwascentralrs1060501194
openSNPrs1060501194
23andMers1060501194
23andMe allrs1060501194
SNPshotrs1060501194
SNPdbers1060501194
MSV3drs1060501194
GWAS Ctlgrs1060501194
Max Magnitude0
ClinVar
Risk rs1060501194(-;-)
Alt rs1060501194(-;-)
Reference Rs1060501194(C;C)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577148delG
CLNSRC
CLNACC RCV000472594.1,