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rs1064793279

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position7676115
GeneTP53
is asnp
is mentioned by
dbSNPrs1064793279
dbSNP (old)rs1064793279
ClinGenrs1064793279
ebirs1064793279
HLIrs1064793279
Exacrs1064793279
Gnomadrs1064793279
Varsomers1064793279
Maprs1064793279
PheGenIrs1064793279
Biobankrs1064793279
1000 genomesrs1064793279
hgdprs1064793279
ensemblrs1064793279
gopubmedrs1064793279
geneviewrs1064793279
scholarrs1064793279
googlers1064793279
pharmgkbrs1064793279
gwascentralrs1064793279
openSNPrs1064793279
23andMers1064793279
23andMe allrs1064793279
SNPshotrs1064793279
SNPdbers1064793279
MSV3drs1064793279
GWAS Ctlgrs1064793279
Max Magnitude0
ClinVar
Risk rs1064793279(-;-)
Alt rs1064793279(-;-)
Reference Rs1064793279(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7579433delG
CLNSRC
CLNACC RCV000486807.1,