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rs786202222

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202222(A;A)
Make rs786202222(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674916
GeneTP53
is asnp
is mentioned by
dbSNPrs786202222
ebirs786202222
HLIrs786202222
Exacrs786202222
Varsomers786202222
Maprs786202222
PheGenIrs786202222
hapmaprs786202222
1000 genomesrs786202222
hgdprs786202222
ensemblrs786202222
gopubmedrs786202222
geneviewrs786202222
scholarrs786202222
googlers786202222
pharmgkbrs786202222
gwascentralrs786202222
openSNPrs786202222
23andMers786202222
23andMe allrs786202222
SNP Nexus

SNPshotrs786202222
SNPdbers786202222
MSV3drs786202222
GWAS Ctlgrs786202222
Max Magnitude0
ClinVar
Risk rs786202222(A;A)
Alt rs786202222(A;A)
Reference rs786202222(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578234A>T
CLNSRC
CLNACC RCV000164938.1,