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rs876659741

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659741(-;-)
Make rs876659741(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635330
GenePALB2
is asnp
is mentioned by
dbSNPrs876659741
ebirs876659741
HLIrs876659741
Exacrs876659741
Varsomers876659741
Maprs876659741
PheGenIrs876659741
hapmaprs876659741
1000 genomesrs876659741
hgdprs876659741
ensemblrs876659741
gopubmedrs876659741
geneviewrs876659741
scholarrs876659741
googlers876659741
pharmgkbrs876659741
gwascentralrs876659741
openSNPrs876659741
23andMers876659741
23andMe allrs876659741
SNP Nexus

SNPshotrs876659741
SNPdbers876659741
MSV3drs876659741
GWAS Ctlgrs876659741
Max Magnitude0
ClinVar
Risk rs876659741(;)
Alt rs876659741(;)
Reference rs876659741(G;G)
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.23646651delC
CLNSRC
CLNACC RCV000219937.1,