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rs876658136

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876658136(-;-)
Make rs876658136(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23607967
GenePALB2
is asnp
is mentioned by
dbSNPrs876658136
ebirs876658136
HLIrs876658136
Exacrs876658136
Varsomers876658136
Maprs876658136
PheGenIrs876658136
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1000 genomesrs876658136
hgdprs876658136
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23andMers876658136
23andMe allrs876658136
SNP Nexus

SNPshotrs876658136
SNPdbers876658136
MSV3drs876658136
GWAS Ctlgrs876658136
Max Magnitude0
ClinVar
Risk rs876658136(;)
Alt rs876658136(;)
Reference rs876658136(TG;TG)
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.23619288_23619289delCA
CLNSRC
CLNACC RCV000215931.1,