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rs730882019

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882019(-;-)
Make rs730882019(-;C)
Make rs730882019(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675156
GeneTP53
is asnp
is mentioned by
dbSNPrs730882019
ebirs730882019
HLIrs730882019
Exacrs730882019
Varsomers730882019
Maprs730882019
PheGenIrs730882019
hapmaprs730882019
1000 genomesrs730882019
hgdprs730882019
ensemblrs730882019
gopubmedrs730882019
geneviewrs730882019
scholarrs730882019
googlers730882019
pharmgkbrs730882019
gwascentralrs730882019
openSNPrs730882019
23andMers730882019
23andMe allrs730882019
SNP Nexus

SNPshotrs730882019
SNPdbers730882019
MSV3drs730882019
GWAS Ctlgrs730882019
Max Magnitude0
ClinVar
Risk rs730882019(C;C)
Alt rs730882019(C;C)
Reference rs730882019(;)
Significance Pathogenic
Disease Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578475dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013157.20, RCV000161060.1,