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rs786202799

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202799(A;G)
Make rs786202799(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675238
GeneTP53
is asnp
is mentioned by
dbSNPrs786202799
ebirs786202799
HLIrs786202799
Exacrs786202799
Varsomers786202799
Maprs786202799
PheGenIrs786202799
hapmaprs786202799
1000 genomesrs786202799
hgdprs786202799
ensemblrs786202799
gopubmedrs786202799
geneviewrs786202799
scholarrs786202799
googlers786202799
pharmgkbrs786202799
gwascentralrs786202799
openSNPrs786202799
23andMers786202799
23andMe allrs786202799
SNP Nexus

SNPshotrs786202799
SNPdbers786202799
MSV3drs786202799
GWAS Ctlgrs786202799
Max Magnitude0
ClinVar
Risk rs786202799(G;G)
Alt rs786202799(G;G)
Reference rs786202799(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578556T>C
CLNSRC
CLNACC RCV000165794.1,