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rs1060501197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501197(-;-)
Make rs1060501197(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674247
GeneTP53
is asnp
is mentioned by
dbSNPrs1060501197
dbSNP (classic)rs1060501197
ClinGenrs1060501197
ebirs1060501197
HLIrs1060501197
Exacrs1060501197
Gnomadrs1060501197
Varsomers1060501197
LitVarrs1060501197
Maprs1060501197
PheGenIrs1060501197
Biobankrs1060501197
1000 genomesrs1060501197
hgdprs1060501197
ensemblrs1060501197
geneviewrs1060501197
scholarrs1060501197
googlers1060501197
pharmgkbrs1060501197
gwascentralrs1060501197
openSNPrs1060501197
23andMers1060501197
23andMe allrs1060501197
SNPshotrs1060501197
SNPdbers1060501197
MSV3drs1060501197
GWAS Ctlgrs1060501197
Max Magnitude0
ClinVar
Risk rs1060501197(-;-)
Alt rs1060501197(-;-)
Reference Rs1060501197(A;A)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577565delT
CLNSRC
CLNACC RCV000460136.1,