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rs730882005

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882005(A;A)
Make rs730882005(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674250
GeneTP53
is asnp
is mentioned by
dbSNPrs730882005
ebirs730882005
HLIrs730882005
Exacrs730882005
Varsomers730882005
Maprs730882005
PheGenIrs730882005
hapmaprs730882005
1000 genomesrs730882005
hgdprs730882005
ensemblrs730882005
gopubmedrs730882005
geneviewrs730882005
scholarrs730882005
googlers730882005
pharmgkbrs730882005
gwascentralrs730882005
openSNPrs730882005
23andMers730882005
23andMe allrs730882005
SNP Nexus

SNPshotrs730882005
SNPdbers730882005
MSV3drs730882005
GWAS Ctlgrs730882005
Max Magnitude0
ClinVar
Risk rs730882005(A;A)
Alt rs730882005(A;A)
Reference rs730882005(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7577568C>T
CLNSRC
CLNACC RCV000161034.4, RCV000167907.1, RCV000235220.1,