Have questions? Visit https://www.reddit.com/r/SNPedia

rs730882004

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882004(A;G)
Make rs730882004(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674254
GeneTP53
is asnp
is mentioned by
dbSNPrs730882004
ebirs730882004
HLIrs730882004
Exacrs730882004
Varsomers730882004
Maprs730882004
PheGenIrs730882004
hapmaprs730882004
1000 genomesrs730882004
hgdprs730882004
ensemblrs730882004
gopubmedrs730882004
geneviewrs730882004
scholarrs730882004
googlers730882004
pharmgkbrs730882004
gwascentralrs730882004
openSNPrs730882004
23andMers730882004
23andMe allrs730882004
SNP Nexus

SNPshotrs730882004
SNPdbers730882004
MSV3drs730882004
GWAS Ctlgrs730882004
Max Magnitude0
ClinVar
Risk rs730882004(G;G)
Alt rs730882004(G;G)
Reference rs730882004(A;A)
Significance Pathogenic
Disease not provided Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not provided Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577572T>C
CLNSRC
CLNACC RCV000161033.2, RCV000200500.1,