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rs1057520607

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520607(G;T)
Make rs1057520607(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673740
GeneTP53
is asnp
is mentioned by
dbSNPrs1057520607
dbSNP (old)rs1057520607
ClinGenrs1057520607
ebirs1057520607
HLIrs1057520607
Exacrs1057520607
Gnomadrs1057520607
Varsomers1057520607
Maprs1057520607
PheGenIrs1057520607
Biobankrs1057520607
1000 genomesrs1057520607
hgdprs1057520607
ensemblrs1057520607
gopubmedrs1057520607
geneviewrs1057520607
scholarrs1057520607
googlers1057520607
pharmgkbrs1057520607
gwascentralrs1057520607
openSNPrs1057520607
23andMers1057520607
23andMe allrs1057520607
SNPshotrs1057520607
SNPdbers1057520607
MSV3drs1057520607
GWAS Ctlgrs1057520607
Max Magnitude0
ClinVar
Risk rs1057520607(T;T)
Alt rs1057520607(T;T)
Reference Rs1057520607(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7577058C>A
CLNSRC
CLNACC RCV000433836.1,