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rs587781702

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781702(A;A)
Make rs587781702(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673609
GeneTP53
is asnp
is mentioned by
dbSNPrs587781702
ebirs587781702
HLIrs587781702
Exacrs587781702
Varsomers587781702
Maprs587781702
PheGenIrs587781702
hapmaprs587781702
1000 genomesrs587781702
hgdprs587781702
ensemblrs587781702
gopubmedrs587781702
geneviewrs587781702
scholarrs587781702
googlers587781702
pharmgkbrs587781702
gwascentralrs587781702
openSNPrs587781702
23andMers587781702
23andMe allrs587781702
SNP Nexus

SNPshotrs587781702
SNPdbers587781702
MSV3drs587781702
GWAS Ctlgrs587781702
Max Magnitude0
ClinVar
Risk rs587781702(A;A)
Alt rs587781702(A;A)
Reference rs587781702(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7576927C>T
CLNSRC
CLNACC RCV000129871.2,