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rs587780066

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780066(-;-)
Make rs587780066(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676041
GeneTP53
is asnp
is mentioned by
dbSNPrs587780066
ebirs587780066
HLIrs587780066
Exacrs587780066
Varsomers587780066
Maprs587780066
PheGenIrs587780066
hapmaprs587780066
1000 genomesrs587780066
hgdprs587780066
ensemblrs587780066
gopubmedrs587780066
geneviewrs587780066
scholarrs587780066
googlers587780066
pharmgkbrs587780066
gwascentralrs587780066
openSNPrs587780066
23andMers587780066
23andMe allrs587780066
SNP Nexus

SNPshotrs587780066
SNPdbers587780066
MSV3drs587780066
GWAS Ctlgrs587780066
Max Magnitude0
ClinVar
Risk rs587780066(;)
Alt rs587780066(;)
Reference rs587780066(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579359delG
CLNSRC
CLNACC RCV000115718.2,