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rs876658855

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658855(-;-)
Make rs876658855(-;TAA)
Make rs876658855(TAA;TAA)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23630011
GenePALB2
is asnp
is mentioned by
dbSNPrs876658855
ebirs876658855
HLIrs876658855
Exacrs876658855
Varsomers876658855
Maprs876658855
PheGenIrs876658855
hapmaprs876658855
1000 genomesrs876658855
hgdprs876658855
ensemblrs876658855
gopubmedrs876658855
geneviewrs876658855
scholarrs876658855
googlers876658855
pharmgkbrs876658855
gwascentralrs876658855
openSNPrs876658855
23andMers876658855
23andMe allrs876658855
SNP Nexus

SNPshotrs876658855
SNPdbers876658855
MSV3drs876658855
GWAS Ctlgrs876658855
Max Magnitude0
ClinVar
Risk rs876658855(TAA;TAA)
Alt rs876658855(TAA;TAA)
Reference rs876658855(;)
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.23641332_23641333insTTA
CLNSRC
CLNACC RCV000222029.1,