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rs730882029

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882029(C;T)
Make rs730882029(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7670685
GeneTP53
is asnp
is mentioned by
dbSNPrs730882029
ebirs730882029
HLIrs730882029
Exacrs730882029
Varsomers730882029
Maprs730882029
PheGenIrs730882029
hapmaprs730882029
1000 genomesrs730882029
hgdprs730882029
ensemblrs730882029
gopubmedrs730882029
geneviewrs730882029
scholarrs730882029
googlers730882029
pharmgkbrs730882029
gwascentralrs730882029
openSNPrs730882029
23andMers730882029
23andMe allrs730882029
SNP Nexus

SNPshotrs730882029
SNPdbers730882029
MSV3drs730882029
GWAS Ctlgrs730882029
Max Magnitude0
ClinVar
Risk rs730882029(T;T)
Alt rs730882029(T;T)
Reference rs730882029(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.7574003G>A
CLNSRC
CLNACC RCV000161074.3, RCV000213069.1,