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rs863223301

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223301(-;GCCATGG)
Make rs863223301(GCCATGG;GCCATGG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675130
GeneTP53
is asnp
is mentioned by
dbSNPrs863223301
ClinGenrs863223301
ebirs863223301
HLIrs863223301
Exacrs863223301
Varsomers863223301
Maprs863223301
PheGenIrs863223301
hapmaprs863223301
1000 genomesrs863223301
hgdprs863223301
ensemblrs863223301
gopubmedrs863223301
geneviewrs863223301
scholarrs863223301
googlers863223301
pharmgkbrs863223301
gwascentralrs863223301
openSNPrs863223301
23andMers863223301
23andMe allrs863223301
SNP Nexus

SNPshotrs863223301
SNPdbers863223301
MSV3drs863223301
GWAS Ctlgrs863223301
Max Magnitude0
ClinVar
Risk rs863223301(GCCATGG;GCCATGG)
Alt rs863223301(GCCATGG;GCCATGG)
Reference Rs863223301(-;-)
Significance Pathogenic
Disease Choroid plexus papilloma Osteosarcoma
Variation info
Gene TP53
CLNDBN Choroid plexus papilloma Osteosarcoma
Reversed 1
HGVS NC_000017.10:g.7578449_7578455dupCCATGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000013179.23, RCV000013180.22,