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rs786203589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAGATGTTTTGCCAAC;AAGATGTTTTGCCAAC) 0 common in clinvar
Make rs786203589(-;-)
Make rs786203589(-;AAGATGTTTTGCCAAC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675203
GeneTP53
is asnp
is mentioned by
dbSNPrs786203589
ClinGenrs786203589
ebirs786203589
HLIrs786203589
Exacrs786203589
Varsomers786203589
Maprs786203589
PheGenIrs786203589
hapmaprs786203589
1000 genomesrs786203589
hgdprs786203589
ensemblrs786203589
gopubmedrs786203589
geneviewrs786203589
scholarrs786203589
googlers786203589
pharmgkbrs786203589
gwascentralrs786203589
openSNPrs786203589
23andMers786203589
23andMe allrs786203589
SNP Nexus

SNPshotrs786203589
SNPdbers786203589
MSV3drs786203589
GWAS Ctlgrs786203589
Max Magnitude0
ClinVar
Risk rs786203589(-;-)
Alt rs786203589(-;-)
Reference Rs786203589(AAGATGTTTTGCCAAC;AAGATGTTTTGCCAAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578521_7578536del16
CLNSRC
CLNACC RCV000166969.1,