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rs1064793881

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position7673784
GeneTP53
is asnp
is mentioned by
dbSNPrs1064793881
dbSNP (old)rs1064793881
ClinGenrs1064793881
ebirs1064793881
HLIrs1064793881
Exacrs1064793881
Gnomadrs1064793881
Varsomers1064793881
Maprs1064793881
PheGenIrs1064793881
Biobankrs1064793881
1000 genomesrs1064793881
hgdprs1064793881
ensemblrs1064793881
gopubmedrs1064793881
geneviewrs1064793881
scholarrs1064793881
googlers1064793881
pharmgkbrs1064793881
gwascentralrs1064793881
openSNPrs1064793881
23andMers1064793881
23andMe allrs1064793881
SNPshotrs1064793881
SNPdbers1064793881
MSV3drs1064793881
GWAS Ctlgrs1064793881
Max Magnitude0
ClinVar
Risk rs1064793881(A;A)
Alt rs1064793881(A;A)
Reference Rs1064793881(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577102C>T
CLNSRC
CLNACC RCV000484876.1, RCV000492354.1,