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rs55863639

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55863639(A;A)
Make rs55863639(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675994
GeneTP53
is asnp
is mentioned by
dbSNPrs55863639
ebirs55863639
HLIrs55863639
Exacrs55863639
Varsomers55863639
Maprs55863639
PheGenIrs55863639
hapmaprs55863639
1000 genomesrs55863639
hgdprs55863639
ensemblrs55863639
gopubmedrs55863639
geneviewrs55863639
scholarrs55863639
googlers55863639
pharmgkbrs55863639
gwascentralrs55863639
openSNPrs55863639
23andMers55863639
23andMe allrs55863639
SNP Nexus

SNPshotrs55863639
SNPdbers55863639
MSV3drs55863639
GWAS Ctlgrs55863639
Max Magnitude0
ClinVar
Risk rs55863639(A,T;A,T)
Alt rs55863639(A,T;A,T)
Reference rs55863639(C;C)
Significance Pathogenic
Disease Li-Fraumeni syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.7579312C>A; NC_000017.10:g.7579312C>T
CLNSRC
CLNACC RCV000229813.1, RCV000154460.1, RCV000218743.1,