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rs876659063

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659063(-;-)
Make rs876659063(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23641123
GeneDCTN5, PALB2
is asnp
is mentioned by
dbSNPrs876659063
ebirs876659063
HLIrs876659063
Exacrs876659063
Varsomers876659063
Maprs876659063
PheGenIrs876659063
hapmaprs876659063
1000 genomesrs876659063
hgdprs876659063
ensemblrs876659063
gopubmedrs876659063
geneviewrs876659063
scholarrs876659063
googlers876659063
pharmgkbrs876659063
gwascentralrs876659063
openSNPrs876659063
23andMers876659063
23andMe allrs876659063
SNP Nexus

SNPshotrs876659063
SNPdbers876659063
MSV3drs876659063
GWAS Ctlgrs876659063
Max Magnitude0
ClinVar
Risk rs876659063(;)
Alt rs876659063(;)
Reference rs876659063(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2 DCTN5
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23652444delT
CLNSRC
CLNACC RCV000218745.1,