Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658431

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658431(-;-)
Make rs876658431(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635340
GenePALB2
is asnp
is mentioned by
dbSNPrs876658431
ebirs876658431
HLIrs876658431
Exacrs876658431
Varsomers876658431
Maprs876658431
PheGenIrs876658431
hapmaprs876658431
1000 genomesrs876658431
hgdprs876658431
ensemblrs876658431
gopubmedrs876658431
geneviewrs876658431
scholarrs876658431
googlers876658431
pharmgkbrs876658431
gwascentralrs876658431
openSNPrs876658431
23andMers876658431
23andMe allrs876658431
SNP Nexus

SNPshotrs876658431
SNPdbers876658431
MSV3drs876658431
GWAS Ctlgrs876658431
Max Magnitude0
ClinVar
Risk rs876658431(;)
Alt rs876658431(;)
Reference rs876658431(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23646661delA
CLNSRC
CLNACC RCV000218688.1,