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rs876659697

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659697(-;-)
Make rs876659697(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629874
GenePALB2
is asnp
is mentioned by
dbSNPrs876659697
ebirs876659697
HLIrs876659697
Exacrs876659697
Varsomers876659697
Maprs876659697
PheGenIrs876659697
hapmaprs876659697
1000 genomesrs876659697
hgdprs876659697
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googlers876659697
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openSNPrs876659697
23andMers876659697
23andMe allrs876659697
SNP Nexus

SNPshotrs876659697
SNPdbers876659697
MSV3drs876659697
GWAS Ctlgrs876659697
Max Magnitude0
ClinVar
Risk rs876659697(;)
Alt rs876659697(;)
Reference rs876659697(T;T)
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.23641195delA
CLNSRC
CLNACC RCV000214754.1,