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rs786202055

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202055(-;-)
Make rs786202055(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7673714
GeneTP53
is asnp
is mentioned by
dbSNPrs786202055
ebirs786202055
HLIrs786202055
Exacrs786202055
Varsomers786202055
Maprs786202055
PheGenIrs786202055
hapmaprs786202055
1000 genomesrs786202055
hgdprs786202055
ensemblrs786202055
gopubmedrs786202055
geneviewrs786202055
scholarrs786202055
googlers786202055
pharmgkbrs786202055
gwascentralrs786202055
openSNPrs786202055
23andMers786202055
23andMe allrs786202055
SNP Nexus

SNPshotrs786202055
SNPdbers786202055
MSV3drs786202055
GWAS Ctlgrs786202055
Max Magnitude0
ClinVar
Risk rs786202055(;)
Alt rs786202055(;)
Reference rs786202055(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577032delC
CLNSRC
CLNACC RCV000164675.1,