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rs1064796124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCCCCTG;GCCCCTG) 0 common in clinvar
Chromosome17
Position7676090
GeneTP53
is asnp
is mentioned by
dbSNPrs1064796124
dbSNP (old)rs1064796124
ClinGenrs1064796124
ebirs1064796124
HLIrs1064796124
Exacrs1064796124
Gnomadrs1064796124
Varsomers1064796124
Maprs1064796124
PheGenIrs1064796124
Biobankrs1064796124
1000 genomesrs1064796124
hgdprs1064796124
ensemblrs1064796124
gopubmedrs1064796124
geneviewrs1064796124
scholarrs1064796124
googlers1064796124
pharmgkbrs1064796124
gwascentralrs1064796124
openSNPrs1064796124
23andMers1064796124
23andMe allrs1064796124
SNPshotrs1064796124
SNPdbers1064796124
MSV3drs1064796124
GWAS Ctlgrs1064796124
Max Magnitude0
ClinVar
Risk rs1064796124(-;-)
Alt rs1064796124(-;-)
Reference Rs1064796124(GCCCCTG;GCCCCTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7579408_7579414delCAGGGGC
CLNSRC
CLNACC RCV000479803.1,