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rs876660754

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660754(A;A)
Make rs876660754(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7675095
GeneTP53
is asnp
is mentioned by
dbSNPrs876660754
ebirs876660754
HLIrs876660754
Exacrs876660754
Varsomers876660754
Maprs876660754
PheGenIrs876660754
hapmaprs876660754
1000 genomesrs876660754
hgdprs876660754
ensemblrs876660754
gopubmedrs876660754
geneviewrs876660754
scholarrs876660754
googlers876660754
pharmgkbrs876660754
gwascentralrs876660754
openSNPrs876660754
23andMers876660754
23andMe allrs876660754
SNP Nexus

SNPshotrs876660754
SNPdbers876660754
MSV3drs876660754
GWAS Ctlgrs876660754
Max Magnitude0
ClinVar
Risk rs876660754(A;A)
Alt rs876660754(A;A)
Reference rs876660754(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000017.10:g.7578413C>T
CLNSRC
CLNACC RCV000214341.1, RCV000223396.1,