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rs876659341

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659341(-;-)
Make rs876659341(-;T)
Make rs876659341(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635120
GenePALB2
is asnp
is mentioned by
dbSNPrs876659341
ebirs876659341
HLIrs876659341
Exacrs876659341
Varsomers876659341
Maprs876659341
PheGenIrs876659341
hapmaprs876659341
1000 genomesrs876659341
hgdprs876659341
ensemblrs876659341
gopubmedrs876659341
geneviewrs876659341
scholarrs876659341
googlers876659341
pharmgkbrs876659341
gwascentralrs876659341
openSNPrs876659341
23andMers876659341
23andMe allrs876659341
SNP Nexus

SNPshotrs876659341
SNPdbers876659341
MSV3drs876659341
GWAS Ctlgrs876659341
Max Magnitude0
ClinVar
Risk rs876659341(T;T)
Alt rs876659341(T;T)
Reference rs876659341(;)
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.23646441_23646442insA
CLNSRC
CLNACC RCV000217519.1,