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rs730882007

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882007(A;C)
Make rs730882007(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674212
GeneTP53
is asnp
is mentioned by
dbSNPrs730882007
ebirs730882007
HLIrs730882007
Exacrs730882007
Varsomers730882007
Maprs730882007
PheGenIrs730882007
hapmaprs730882007
1000 genomesrs730882007
hgdprs730882007
ensemblrs730882007
gopubmedrs730882007
geneviewrs730882007
scholarrs730882007
googlers730882007
pharmgkbrs730882007
gwascentralrs730882007
openSNPrs730882007
23andMers730882007
23andMe allrs730882007
SNP Nexus

SNPshotrs730882007
SNPdbers730882007
MSV3drs730882007
GWAS Ctlgrs730882007
Max Magnitude0
ClinVar
Risk rs730882007(C;C)
Alt rs730882007(C;C)
Reference rs730882007(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577530T>G
CLNSRC
CLNACC RCV000161037.1,