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rs1057522275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057522275(C;G)
Make rs1057522275(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674246
GeneTP53
is asnp
is mentioned by
dbSNPrs1057522275
dbSNP (old)rs1057522275
ClinGenrs1057522275
ebirs1057522275
HLIrs1057522275
Exacrs1057522275
Gnomadrs1057522275
Varsomers1057522275
LitVarrs1057522275
Maprs1057522275
PheGenIrs1057522275
Biobankrs1057522275
1000 genomesrs1057522275
hgdprs1057522275
ensemblrs1057522275
gopubmedrs1057522275
geneviewrs1057522275
scholarrs1057522275
googlers1057522275
pharmgkbrs1057522275
gwascentralrs1057522275
openSNPrs1057522275
23andMers1057522275
23andMe allrs1057522275
SNPshotrs1057522275
SNPdbers1057522275
MSV3drs1057522275
GWAS Ctlgrs1057522275
Max Magnitude0
ClinVar
Risk rs1057522275(G;G)
Alt rs1057522275(G;G)
Reference Rs1057522275(C;C)
Significance Probable-Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN not specified Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577564G>C
CLNSRC
CLNACC RCV000431317.1, RCV000492173.1,