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rs863223300

From SNPedia

Orientationminus
Make rs863223300(-;-)
Make rs863223300(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675080
GeneTP53
is asnp
is mentioned by
dbSNPrs863223300
ebirs863223300
HLIrs863223300
Exacrs863223300
Varsomers863223300
Maprs863223300
PheGenIrs863223300
hapmaprs863223300
1000 genomesrs863223300
hgdprs863223300
ensemblrs863223300
gopubmedrs863223300
geneviewrs863223300
scholarrs863223300
googlers863223300
pharmgkbrs863223300
gwascentralrs863223300
openSNPrs863223300
23andMers863223300
23andMe allrs863223300
SNP Nexus

SNPshotrs863223300
SNPdbers863223300
MSV3drs863223300
GWAS Ctlgrs863223300
Max Magnitude
ClinVar
Risk rs863223300(;)
Alt rs863223300(;)
Reference rs863223300(C;C)
Significance Pathogenic
Disease Li-Fraumeni syndrome 1 Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7578398delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013176.22, RCV000215848.1,