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rs780442292

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs780442292(A;C)
Make rs780442292(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7675211
GeneTP53
is asnp
is mentioned by
dbSNPrs780442292
ebirs780442292
HLIrs780442292
Exacrs780442292
Varsomers780442292
Maprs780442292
PheGenIrs780442292
hapmaprs780442292
1000 genomesrs780442292
hgdprs780442292
ensemblrs780442292
gopubmedrs780442292
geneviewrs780442292
scholarrs780442292
googlers780442292
pharmgkbrs780442292
gwascentralrs780442292
openSNPrs780442292
23andMers780442292
23andMe allrs780442292
SNP Nexus

SNPshotrs780442292
SNPdbers780442292
MSV3drs780442292
GWAS Ctlgrs780442292
Max Magnitude0
ClinVar
Risk rs780442292(C;C)
Alt rs780442292(C;C)
Reference rs780442292(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.7578529A>C
CLNSRC
CLNACC RCV000214547.1,