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rs1057517840

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1057517840(-;-)
Make rs1057517840(-;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7674904
GeneTP53
is asnp
is mentioned by
dbSNPrs1057517840
dbSNP (old)rs1057517840
ClinGenrs1057517840
ebirs1057517840
HLIrs1057517840
Exacrs1057517840
Gnomadrs1057517840
Varsomers1057517840
Maprs1057517840
PheGenIrs1057517840
Biobankrs1057517840
1000 genomesrs1057517840
hgdprs1057517840
ensemblrs1057517840
gopubmedrs1057517840
geneviewrs1057517840
scholarrs1057517840
googlers1057517840
pharmgkbrs1057517840
gwascentralrs1057517840
openSNPrs1057517840
23andMers1057517840
23andMe allrs1057517840
SNPshotrs1057517840
SNPdbers1057517840
MSV3drs1057517840
GWAS Ctlgrs1057517840
Max Magnitude0
ClinVar
Risk rs1057517840(-;-)
Alt rs1057517840(-;-)
Reference Rs1057517840(GA;GA)
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.7578222_7578223delTC
CLNSRC
CLNACC RCV000414120.1, RCV000492427.1,