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rs786203436

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203436(G;G)
Make rs786203436(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675125
GeneTP53
is asnp
is mentioned by
dbSNPrs786203436
ebirs786203436
HLIrs786203436
Exacrs786203436
Varsomers786203436
Maprs786203436
PheGenIrs786203436
hapmaprs786203436
1000 genomesrs786203436
hgdprs786203436
ensemblrs786203436
gopubmedrs786203436
geneviewrs786203436
scholarrs786203436
googlers786203436
pharmgkbrs786203436
gwascentralrs786203436
openSNPrs786203436
23andMers786203436
23andMe allrs786203436
SNP Nexus

SNPshotrs786203436
SNPdbers786203436
MSV3drs786203436
GWAS Ctlgrs786203436
Max Magnitude0
ClinVar
Risk rs786203436(G;G)
Alt rs786203436(G;G)
Reference rs786203436(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578443A>C
CLNSRC
CLNACC RCV000166739.1,