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rs587778720

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778720(A;A)
Make rs587778720(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674893
GeneTP53
is asnp
is mentioned by
dbSNPrs587778720
ebirs587778720
HLIrs587778720
Exacrs587778720
Varsomers587778720
Maprs587778720
PheGenIrs587778720
hapmaprs587778720
1000 genomesrs587778720
hgdprs587778720
ensemblrs587778720
gopubmedrs587778720
geneviewrs587778720
scholarrs587778720
googlers587778720
pharmgkbrs587778720
gwascentralrs587778720
openSNPrs587778720
23andMers587778720
23andMe allrs587778720
SNP Nexus

SNPshotrs587778720
SNPdbers587778720
MSV3drs587778720
GWAS Ctlgrs587778720
Max Magnitude0
ClinVar
Risk rs587778720(A,C;A,C)
Alt rs587778720(A,C;A,C)
Reference rs587778720(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not specified Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not specified Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Reversed 1
HGVS NC_000017.10:g.7578211C>G; NC_000017.10:g.7578211C>T
CLNSRC Inc.
CLNACC RCV000220461.1, RCV000122176.1, RCV000123099.2, RCV000130072.3, RCV000144664.1,