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rs876658983

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658983(A;A)
Make rs876658983(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626291
GenePALB2
is asnp
is mentioned by
dbSNPrs876658983
ebirs876658983
HLIrs876658983
Exacrs876658983
Varsomers876658983
Maprs876658983
PheGenIrs876658983
hapmaprs876658983
1000 genomesrs876658983
hgdprs876658983
ensemblrs876658983
gopubmedrs876658983
geneviewrs876658983
scholarrs876658983
googlers876658983
pharmgkbrs876658983
gwascentralrs876658983
openSNPrs876658983
23andMers876658983
23andMe allrs876658983
SNP Nexus

SNPshotrs876658983
SNPdbers876658983
MSV3drs876658983
GWAS Ctlgrs876658983
Max Magnitude0
ClinVar
Risk rs876658983(A;A)
Alt rs876658983(A;A)
Reference rs876658983(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.23637612C>T
CLNSRC
CLNACC RCV000216899.1,