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rs876659571

From SNPedia

Orientationminus
Geno Mag Summary
(TGAA;TGAA) 0 common in clinvar
Make rs876659571(-;-)
Make rs876659571(-;TGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629863
GenePALB2
is asnp
is mentioned by
dbSNPrs876659571
ebirs876659571
HLIrs876659571
Exacrs876659571
Varsomers876659571
Maprs876659571
PheGenIrs876659571
hapmaprs876659571
1000 genomesrs876659571
hgdprs876659571
ensemblrs876659571
gopubmedrs876659571
geneviewrs876659571
scholarrs876659571
googlers876659571
pharmgkbrs876659571
gwascentralrs876659571
openSNPrs876659571
23andMers876659571
23andMe allrs876659571
SNP Nexus

SNPshotrs876659571
SNPdbers876659571
MSV3drs876659571
GWAS Ctlgrs876659571
Max Magnitude0
ClinVar
Risk rs876659571(;)
Alt rs876659571(;)
Reference rs876659571(TGAA;TGAA)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000016.9:g.23641184_23641187delTTCA
CLNSRC
CLNACC RCV000213608.1, RCV000235354.1,