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rs1060501212

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TTA;TTA) 0 common in clinvar
Make rs1060501212(-;-)
Make rs1060501212(-;TTA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674973
GeneTP53
is asnp
is mentioned by
dbSNPrs1060501212
dbSNP (old)rs1060501212
ClinGenrs1060501212
ebirs1060501212
HLIrs1060501212
Exacrs1060501212
Gnomadrs1060501212
Varsomers1060501212
Maprs1060501212
PheGenIrs1060501212
Biobankrs1060501212
1000 genomesrs1060501212
hgdprs1060501212
ensemblrs1060501212
gopubmedrs1060501212
geneviewrs1060501212
scholarrs1060501212
googlers1060501212
pharmgkbrs1060501212
gwascentralrs1060501212
openSNPrs1060501212
23andMers1060501212
23andMe allrs1060501212
SNPshotrs1060501212
SNPdbers1060501212
MSV3drs1060501212
GWAS Ctlgrs1060501212
Max Magnitude0
ClinVar
Risk rs1060501212(-;-)
Alt rs1060501212(-;-)
Reference Rs1060501212(TTA;TTA)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578291_7578293delTAA
CLNSRC
CLNACC RCV000464864.1,