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rs876659378

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659378(-;-)
Make rs876659378(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23621448
GenePALB2
is asnp
is mentioned by
dbSNPrs876659378
ebirs876659378
HLIrs876659378
Exacrs876659378
Varsomers876659378
Maprs876659378
PheGenIrs876659378
hapmaprs876659378
1000 genomesrs876659378
hgdprs876659378
ensemblrs876659378
gopubmedrs876659378
geneviewrs876659378
scholarrs876659378
googlers876659378
pharmgkbrs876659378
gwascentralrs876659378
openSNPrs876659378
23andMers876659378
23andMe allrs876659378
SNP Nexus

SNPshotrs876659378
SNPdbers876659378
MSV3drs876659378
GWAS Ctlgrs876659378
Max Magnitude0
ClinVar
Risk rs876659378(;)
Alt rs876659378(;)
Reference rs876659378(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.23632769delA
CLNSRC
CLNACC RCV000217162.1,