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rs876659036

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659036(G;T)
Make rs876659036(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23622997
GenePALB2
is asnp
is mentioned by
dbSNPrs876659036
ebirs876659036
HLIrs876659036
Exacrs876659036
Varsomers876659036
Maprs876659036
PheGenIrs876659036
hapmaprs876659036
1000 genomesrs876659036
hgdprs876659036
ensemblrs876659036
gopubmedrs876659036
geneviewrs876659036
scholarrs876659036
googlers876659036
pharmgkbrs876659036
gwascentralrs876659036
openSNPrs876659036
23andMers876659036
23andMe allrs876659036
SNP Nexus

SNPshotrs876659036
SNPdbers876659036
MSV3drs876659036
GWAS Ctlgrs876659036
Max Magnitude0
ClinVar
Risk rs876659036(T;T)
Alt rs876659036(T;T)
Reference rs876659036(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.23634318C>A
CLNSRC
CLNACC RCV000219424.1,