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rs786201838

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201838(A;G)
Make rs786201838(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674953
GeneTP53
is asnp
is mentioned by
dbSNPrs786201838
ebirs786201838
HLIrs786201838
Exacrs786201838
Varsomers786201838
Maprs786201838
PheGenIrs786201838
hapmaprs786201838
1000 genomesrs786201838
hgdprs786201838
ensemblrs786201838
gopubmedrs786201838
geneviewrs786201838
scholarrs786201838
googlers786201838
pharmgkbrs786201838
gwascentralrs786201838
openSNPrs786201838
23andMers786201838
23andMe allrs786201838
SNP Nexus

SNPshotrs786201838
SNPdbers786201838
MSV3drs786201838
GWAS Ctlgrs786201838
Max Magnitude0
ClinVar
Risk rs786201838(G,T;G,T)
Alt rs786201838(G,T;G,T)
Reference rs786201838(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578271T>A; NC_000017.10:g.7578271T>C
CLNSRC
CLNACC RCV000165315.1, RCV000164329.1,