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rs876660643

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660643(-;-)
Make rs876660643(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626349
GenePALB2
is asnp
is mentioned by
dbSNPrs876660643
ebirs876660643
HLIrs876660643
Exacrs876660643
Varsomers876660643
Maprs876660643
PheGenIrs876660643
hapmaprs876660643
1000 genomesrs876660643
hgdprs876660643
ensemblrs876660643
gopubmedrs876660643
geneviewrs876660643
scholarrs876660643
googlers876660643
pharmgkbrs876660643
gwascentralrs876660643
openSNPrs876660643
23andMers876660643
23andMe allrs876660643
SNP Nexus

SNPshotrs876660643
SNPdbers876660643
MSV3drs876660643
GWAS Ctlgrs876660643
Max Magnitude0
ClinVar
Risk rs876660643(;)
Alt rs876660643(;)
Reference rs876660643(A;A)
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.23637670delT
CLNSRC
CLNACC RCV000215674.1,