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rs876658192

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658192(-;-)
Make rs876658192(-;T)
Make rs876658192(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635838
GenePALB2
is asnp
is mentioned by
dbSNPrs876658192
ebirs876658192
HLIrs876658192
Exacrs876658192
Varsomers876658192
Maprs876658192
PheGenIrs876658192
hapmaprs876658192
1000 genomesrs876658192
hgdprs876658192
ensemblrs876658192
gopubmedrs876658192
geneviewrs876658192
scholarrs876658192
googlers876658192
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gwascentralrs876658192
openSNPrs876658192
23andMers876658192
23andMe allrs876658192
SNP Nexus

SNPshotrs876658192
SNPdbers876658192
MSV3drs876658192
GWAS Ctlgrs876658192
Max Magnitude0
ClinVar
Risk rs876658192(T;T)
Alt rs876658192(T;T)
Reference rs876658192(;)
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.23647160dupA
CLNSRC
CLNACC RCV000219994.1,