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rs786202315

From SNPedia

Orientationminus
Geno Mag Summary
(GGTGCCCTATGAGCCG;GGTGCCCTATGAGCCG) 0 common in clinvar
Make rs786202315(-;-)
Make rs786202315(-;GGTGCCCTATGAGCCG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674865
GeneTP53
is asnp
is mentioned by
dbSNPrs786202315
ebirs786202315
HLIrs786202315
Exacrs786202315
Varsomers786202315
Maprs786202315
PheGenIrs786202315
hapmaprs786202315
1000 genomesrs786202315
hgdprs786202315
ensemblrs786202315
gopubmedrs786202315
geneviewrs786202315
scholarrs786202315
googlers786202315
pharmgkbrs786202315
gwascentralrs786202315
openSNPrs786202315
23andMers786202315
23andMe allrs786202315
SNP Nexus

SNPshotrs786202315
SNPdbers786202315
MSV3drs786202315
GWAS Ctlgrs786202315
Max Magnitude0
ClinVar
Risk rs786202315(;)
Alt rs786202315(;)
Reference rs786202315(GGTGCCCTATGAGCCG;GGTGCCCTATGAGCCG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578183_7578198del16
CLNSRC
CLNACC RCV000165061.1,