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rs876659328

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659328(-;-)
Make rs876659328(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635888
GenePALB2
is asnp
is mentioned by
dbSNPrs876659328
ebirs876659328
HLIrs876659328
Exacrs876659328
Varsomers876659328
Maprs876659328
PheGenIrs876659328
hapmaprs876659328
1000 genomesrs876659328
hgdprs876659328
ensemblrs876659328
gopubmedrs876659328
geneviewrs876659328
scholarrs876659328
googlers876659328
pharmgkbrs876659328
gwascentralrs876659328
openSNPrs876659328
23andMers876659328
23andMe allrs876659328
SNP Nexus

SNPshotrs876659328
SNPdbers876659328
MSV3drs876659328
GWAS Ctlgrs876659328
Max Magnitude0
ClinVar
Risk rs876659328(;)
Alt rs876659328(;)
Reference rs876659328(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.23647209delT
CLNSRC
CLNACC RCV000217719.1,