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rs193920789

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193920789(G;G)
Make rs193920789(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674249
GeneTP53
is asnp
is mentioned by
dbSNPrs193920789
ebirs193920789
HLIrs193920789
Exacrs193920789
Varsomers193920789
Maprs193920789
PheGenIrs193920789
hapmaprs193920789
1000 genomesrs193920789
hgdprs193920789
ensemblrs193920789
gopubmedrs193920789
geneviewrs193920789
scholarrs193920789
googlers193920789
pharmgkbrs193920789
gwascentralrs193920789
openSNPrs193920789
23andMers193920789
23andMe allrs193920789
SNP Nexus

SNPshotrs193920789
SNPdbers193920789
MSV3drs193920789
GWAS Ctlgrs193920789
Max Magnitude0
ClinVar
Risk rs193920789(G;G)
Alt rs193920789(G;G)
Reference rs193920789(T;T)
Significance Pathogenic
Disease Malignant tumor of prostate Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Malignant tumor of prostate Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577567A>C
CLNSRC
CLNACC RCV000149049.1, RCV000203823.1,