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rs876658773

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658773(G;T)
Make rs876658773(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23603662
GenePALB2
is asnp
is mentioned by
dbSNPrs876658773
ebirs876658773
HLIrs876658773
Exacrs876658773
Varsomers876658773
Maprs876658773
PheGenIrs876658773
hapmaprs876658773
1000 genomesrs876658773
hgdprs876658773
ensemblrs876658773
gopubmedrs876658773
geneviewrs876658773
scholarrs876658773
googlers876658773
pharmgkbrs876658773
gwascentralrs876658773
openSNPrs876658773
23andMers876658773
23andMe allrs876658773
SNP Nexus

SNPshotrs876658773
SNPdbers876658773
MSV3drs876658773
GWAS Ctlgrs876658773
Max Magnitude0
ClinVar
Risk rs876658773(T;T)
Alt rs876658773(T;T)
Reference rs876658773(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.23614983C>A
CLNSRC
CLNACC RCV000215626.1,