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rs587780068

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780068(C;T)
Make rs587780068(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7675140
GeneTP53
is asnp
is mentioned by
dbSNPrs587780068
ebirs587780068
HLIrs587780068
Exacrs587780068
Varsomers587780068
Maprs587780068
PheGenIrs587780068
hapmaprs587780068
1000 genomesrs587780068
hgdprs587780068
ensemblrs587780068
gopubmedrs587780068
geneviewrs587780068
scholarrs587780068
googlers587780068
pharmgkbrs587780068
gwascentralrs587780068
openSNPrs587780068
23andMers587780068
23andMe allrs587780068
SNP Nexus

SNPshotrs587780068
SNPdbers587780068
MSV3drs587780068
GWAS Ctlgrs587780068
Max Magnitude0
ClinVar
Risk rs587780068(T;T)
Alt rs587780068(T;T)
Reference rs587780068(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7578458G>A
CLNSRC
CLNACC RCV000115723.6, RCV000213053.1,