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rs876659405

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876659405(-;-)
Make rs876659405(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23636079
GenePALB2
is asnp
is mentioned by
dbSNPrs876659405
ebirs876659405
HLIrs876659405
Exacrs876659405
Varsomers876659405
Maprs876659405
PheGenIrs876659405
hapmaprs876659405
1000 genomesrs876659405
hgdprs876659405
ensemblrs876659405
gopubmedrs876659405
geneviewrs876659405
scholarrs876659405
googlers876659405
pharmgkbrs876659405
gwascentralrs876659405
openSNPrs876659405
23andMers876659405
23andMe allrs876659405
SNP Nexus

SNPshotrs876659405
SNPdbers876659405
MSV3drs876659405
GWAS Ctlgrs876659405
Max Magnitude0
ClinVar
Risk rs876659405(;)
Alt rs876659405(;)
Reference rs876659405(AT;AT)
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.23647400_23647401delAT
CLNSRC
CLNACC RCV000214798.1,