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rs786202514

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202514(-;-)
Make rs786202514(-;GAGGT)
Make rs786202514(GAGGT;GAGGT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7675096
GeneTP53
is asnp
is mentioned by
dbSNPrs786202514
ebirs786202514
HLIrs786202514
Exacrs786202514
Varsomers786202514
Maprs786202514
PheGenIrs786202514
hapmaprs786202514
1000 genomesrs786202514
hgdprs786202514
ensemblrs786202514
gopubmedrs786202514
geneviewrs786202514
scholarrs786202514
googlers786202514
pharmgkbrs786202514
gwascentralrs786202514
openSNPrs786202514
23andMers786202514
23andMe allrs786202514
SNP Nexus

SNPshotrs786202514
SNPdbers786202514
MSV3drs786202514
GWAS Ctlgrs786202514
Max Magnitude0
ClinVar
Risk rs786202514(GAGGT;GAGGT)
Alt rs786202514(GAGGT;GAGGT)
Reference rs786202514(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578415_7578419dupACCTC
CLNSRC
CLNACC RCV000165358.1,