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rs587782144

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782144(A;A)
Make rs587782144(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675139
GeneTP53
is asnp
is mentioned by
dbSNPrs587782144
ebirs587782144
HLIrs587782144
Exacrs587782144
Varsomers587782144
Maprs587782144
PheGenIrs587782144
hapmaprs587782144
1000 genomesrs587782144
hgdprs587782144
ensemblrs587782144
gopubmedrs587782144
geneviewrs587782144
scholarrs587782144
googlers587782144
pharmgkbrs587782144
gwascentralrs587782144
openSNPrs587782144
23andMers587782144
23andMe allrs587782144
SNP Nexus

SNPshotrs587782144
SNPdbers587782144
MSV3drs587782144
GWAS Ctlgrs587782144
Max Magnitude0
ClinVar
Risk rs587782144(A,C;A,C)
Alt rs587782144(A,C;A,C)
Reference rs587782144(G;G)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not specified Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578457C>G; NC_000017.10:g.7578457C>T
CLNSRC
CLNACC RCV000236862.1, RCV000130708.2, RCV000227859.1,