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rs876659326

From SNPedia

Orientationminus
Geno Mag Summary
(CCTTT;CCTTT) 0 common in clinvar
Make rs876659326(-;-)
Make rs876659326(-;CCTTT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635797
GenePALB2
is asnp
is mentioned by
dbSNPrs876659326
ebirs876659326
HLIrs876659326
Exacrs876659326
Varsomers876659326
Maprs876659326
PheGenIrs876659326
hapmaprs876659326
1000 genomesrs876659326
hgdprs876659326
ensemblrs876659326
gopubmedrs876659326
geneviewrs876659326
scholarrs876659326
googlers876659326
pharmgkbrs876659326
gwascentralrs876659326
openSNPrs876659326
23andMers876659326
23andMe allrs876659326
SNP Nexus

SNPshotrs876659326
SNPdbers876659326
MSV3drs876659326
GWAS Ctlgrs876659326
Max Magnitude0
ClinVar
Risk rs876659326(;)
Alt rs876659326(;)
Reference rs876659326(CCTTT;CCTTT)
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.23647118_23647122delAAAGG
CLNSRC
CLNACC RCV000222919.1,