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rs730882017

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882017(-;-)
Make rs730882017(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7669666
GeneTP53
is asnp
is mentioned by
dbSNPrs730882017
ebirs730882017
HLIrs730882017
Exacrs730882017
Varsomers730882017
Maprs730882017
PheGenIrs730882017
hapmaprs730882017
1000 genomesrs730882017
hgdprs730882017
ensemblrs730882017
gopubmedrs730882017
geneviewrs730882017
scholarrs730882017
googlers730882017
pharmgkbrs730882017
gwascentralrs730882017
openSNPrs730882017
23andMers730882017
23andMe allrs730882017
SNP Nexus

SNPshotrs730882017
SNPdbers730882017
MSV3drs730882017
GWAS Ctlgrs730882017
Max Magnitude0
ClinVar
Risk rs730882017(;)
Alt rs730882017(;)
Reference rs730882017(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7572984delC
CLNSRC
CLNACC RCV000161058.2,