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rs587781664

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781664(A;G)
Make rs587781664(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7669692
GeneTP53
is asnp
is mentioned by
dbSNPrs587781664
ebirs587781664
HLIrs587781664
Exacrs587781664
Varsomers587781664
Maprs587781664
PheGenIrs587781664
hapmaprs587781664
1000 genomesrs587781664
hgdprs587781664
ensemblrs587781664
gopubmedrs587781664
geneviewrs587781664
scholarrs587781664
googlers587781664
pharmgkbrs587781664
gwascentralrs587781664
openSNPrs587781664
23andMers587781664
23andMe allrs587781664
SNP Nexus

SNPshotrs587781664
SNPdbers587781664
MSV3drs587781664
GWAS Ctlgrs587781664
Max Magnitude0
ClinVar
Risk rs587781664(G;G)
Alt rs587781664(G;G)
Reference rs587781664(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not provided
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not provided
Reversed 1
HGVS NC_000017.10:g.7573010T>C
CLNSRC
CLNACC RCV000129814.5, RCV000206779.1, RCV000213070.1,