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rs760043106

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs760043106(A;G)
Make rs760043106(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674947
GeneTP53
is asnp
is mentioned by
dbSNPrs760043106
ebirs760043106
HLIrs760043106
Exacrs760043106
Varsomers760043106
Maprs760043106
PheGenIrs760043106
hapmaprs760043106
1000 genomesrs760043106
hgdprs760043106
ensemblrs760043106
gopubmedrs760043106
geneviewrs760043106
scholarrs760043106
googlers760043106
pharmgkbrs760043106
gwascentralrs760043106
openSNPrs760043106
23andMers760043106
23andMe allrs760043106
SNP Nexus

SNPshotrs760043106
SNPdbers760043106
MSV3drs760043106
GWAS Ctlgrs760043106
Max Magnitude0
ClinVar
Risk rs760043106(G;G)
Alt rs760043106(G;G)
Reference rs760043106(A;A)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 0
HGVS NC_000017.10:g.7578265A>G
CLNSRC
CLNACC RCV000198789.2,