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rs876659679

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659679(G;G)
Make rs876659679(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23641108
GeneDCTN5, PALB2
is asnp
is mentioned by
dbSNPrs876659679
ebirs876659679
HLIrs876659679
Exacrs876659679
Varsomers876659679
Maprs876659679
PheGenIrs876659679
hapmaprs876659679
1000 genomesrs876659679
hgdprs876659679
ensemblrs876659679
gopubmedrs876659679
geneviewrs876659679
scholarrs876659679
googlers876659679
pharmgkbrs876659679
gwascentralrs876659679
openSNPrs876659679
23andMers876659679
23andMe allrs876659679
SNP Nexus

SNPshotrs876659679
SNPdbers876659679
MSV3drs876659679
GWAS Ctlgrs876659679
Max Magnitude0
ClinVar
Risk rs876659679(G;G)
Alt rs876659679(G;G)
Reference rs876659679(T;T)
Significance Probable-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.23652429A>C
CLNSRC
CLNACC RCV000221819.1,