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rs786202962

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202962(A;A)
Make rs786202962(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675085
GeneTP53
is asnp
is mentioned by
dbSNPrs786202962
ebirs786202962
HLIrs786202962
Exacrs786202962
Varsomers786202962
Maprs786202962
PheGenIrs786202962
hapmaprs786202962
1000 genomesrs786202962
hgdprs786202962
ensemblrs786202962
gopubmedrs786202962
geneviewrs786202962
scholarrs786202962
googlers786202962
pharmgkbrs786202962
gwascentralrs786202962
openSNPrs786202962
23andMers786202962
23andMe allrs786202962
SNP Nexus

SNPshotrs786202962
SNPdbers786202962
MSV3drs786202962
GWAS Ctlgrs786202962
Max Magnitude0
ClinVar
Risk rs786202962(A;A)
Alt rs786202962(A;A)
Reference rs786202962(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578403C>T
CLNSRC
CLNACC RCV000166045.1,