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rs763098116

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763098116(C;T)
Make rs763098116(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673790
GeneTP53
is asnp
is mentioned by
dbSNPrs763098116
ebirs763098116
HLIrs763098116
Exacrs763098116
Varsomers763098116
Maprs763098116
PheGenIrs763098116
hapmaprs763098116
1000 genomesrs763098116
hgdprs763098116
ensemblrs763098116
gopubmedrs763098116
geneviewrs763098116
scholarrs763098116
googlers763098116
pharmgkbrs763098116
gwascentralrs763098116
openSNPrs763098116
23andMers763098116
23andMe allrs763098116
SNP Nexus

SNPshotrs763098116
SNPdbers763098116
MSV3drs763098116
GWAS Ctlgrs763098116
Max Magnitude0
ClinVar
Risk rs763098116(A,T;A,T)
Alt rs763098116(A,T;A,T)
Reference rs763098116(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.7577108C>T
CLNSRC
CLNACC RCV000165199.1,