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rs876658166

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658166(C;T)
Make rs876658166(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635168
GenePALB2
is asnp
is mentioned by
dbSNPrs876658166
ebirs876658166
HLIrs876658166
Exacrs876658166
Varsomers876658166
Maprs876658166
PheGenIrs876658166
hapmaprs876658166
1000 genomesrs876658166
hgdprs876658166
ensemblrs876658166
gopubmedrs876658166
geneviewrs876658166
scholarrs876658166
googlers876658166
pharmgkbrs876658166
gwascentralrs876658166
openSNPrs876658166
23andMers876658166
23andMe allrs876658166
SNP Nexus

SNPshotrs876658166
SNPdbers876658166
MSV3drs876658166
GWAS Ctlgrs876658166
Max Magnitude0
ClinVar
Risk rs876658166(T;T)
Alt rs876658166(T;T)
Reference rs876658166(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.23646489G>A
CLNSRC
CLNACC RCV000222117.1,