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rs1057523496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523496(G;G)
Make rs1057523496(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7676044
GeneTP53
is asnp
is mentioned by
dbSNPrs1057523496
dbSNP (old)rs1057523496
ClinGenrs1057523496
ebirs1057523496
HLIrs1057523496
Exacrs1057523496
Gnomadrs1057523496
Varsomers1057523496
Maprs1057523496
PheGenIrs1057523496
Biobankrs1057523496
1000 genomesrs1057523496
hgdprs1057523496
ensemblrs1057523496
gopubmedrs1057523496
geneviewrs1057523496
scholarrs1057523496
googlers1057523496
pharmgkbrs1057523496
gwascentralrs1057523496
openSNPrs1057523496
23andMers1057523496
23andMe allrs1057523496
SNPshotrs1057523496
SNPdbers1057523496
MSV3drs1057523496
GWAS Ctlgrs1057523496
Max Magnitude0
ClinVar
Risk rs1057523496(G;G)
Alt rs1057523496(G;G)
Reference Rs1057523496(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7579362A>C
CLNSRC
CLNACC RCV000434126.1,