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rs1060501207

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501207(A;G)
Make rs1060501207(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673839
GeneTP53
is asnp
is mentioned by
dbSNPrs1060501207
dbSNP (old)rs1060501207
ClinGenrs1060501207
ebirs1060501207
HLIrs1060501207
Exacrs1060501207
Gnomadrs1060501207
Varsomers1060501207
Maprs1060501207
PheGenIrs1060501207
Biobankrs1060501207
1000 genomesrs1060501207
hgdprs1060501207
ensemblrs1060501207
gopubmedrs1060501207
geneviewrs1060501207
scholarrs1060501207
googlers1060501207
pharmgkbrs1060501207
gwascentralrs1060501207
openSNPrs1060501207
23andMers1060501207
23andMe allrs1060501207
SNPshotrs1060501207
SNPdbers1060501207
MSV3drs1060501207
GWAS Ctlgrs1060501207
Max Magnitude0
ClinVar
Risk rs1060501207(G;G)
Alt rs1060501207(G;G)
Reference Rs1060501207(A;A)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577157T>C
CLNSRC
CLNACC RCV000464087.1,