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rs876659319

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659319(C;T)
Make rs876659319(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23637946
GenePALB2
is asnp
is mentioned by
dbSNPrs876659319
ebirs876659319
HLIrs876659319
Exacrs876659319
Varsomers876659319
Maprs876659319
PheGenIrs876659319
hapmaprs876659319
1000 genomesrs876659319
hgdprs876659319
ensemblrs876659319
gopubmedrs876659319
geneviewrs876659319
scholarrs876659319
googlers876659319
pharmgkbrs876659319
gwascentralrs876659319
openSNPrs876659319
23andMers876659319
23andMe allrs876659319
SNP Nexus

SNPshotrs876659319
SNPdbers876659319
MSV3drs876659319
GWAS Ctlgrs876659319
Max Magnitude0
ClinVar
Risk rs876659319(T;T)
Alt rs876659319(T;T)
Reference rs876659319(C;C)
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.23649267G>A
CLNSRC
CLNACC RCV000223492.1,