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rs55819519

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55819519(C;T)
Make rs55819519(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7673751
GeneTP53
is asnp
is mentioned by
dbSNPrs55819519
ebirs55819519
HLIrs55819519
Exacrs55819519
Varsomers55819519
Maprs55819519
PheGenIrs55819519
hapmaprs55819519
1000 genomesrs55819519
hgdprs55819519
ensemblrs55819519
gopubmedrs55819519
geneviewrs55819519
scholarrs55819519
googlers55819519
pharmgkbrs55819519
gwascentralrs55819519
openSNPrs55819519
23andMers55819519
23andMe allrs55819519
SNP Nexus

SNPshotrs55819519
SNPdbers55819519
MSV3drs55819519
GWAS Ctlgrs55819519
Max Magnitude0
ClinVar
Risk rs55819519(T;T)
Alt rs55819519(T;T)
Reference rs55819519(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome Li-Fraumeni syndrome 1 not specified
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome Li-Fraumeni syndrome 1 not specified
Reversed 0
HGVS NC_000017.10:g.7577069C>T
CLNSRC
CLNACC RCV000115740.5, RCV000148914.4, RCV000195926.1, RCV000213061.1,