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rs876658695

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658695(-;-)
Make rs876658695(-;ATTG)
Make rs876658695(ATTG;ATTG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23603543
GenePALB2
is asnp
is mentioned by
dbSNPrs876658695
ebirs876658695
HLIrs876658695
Exacrs876658695
Varsomers876658695
Maprs876658695
PheGenIrs876658695
hapmaprs876658695
1000 genomesrs876658695
hgdprs876658695
ensemblrs876658695
gopubmedrs876658695
geneviewrs876658695
scholarrs876658695
googlers876658695
pharmgkbrs876658695
gwascentralrs876658695
openSNPrs876658695
23andMers876658695
23andMe allrs876658695
SNP Nexus

SNPshotrs876658695
SNPdbers876658695
MSV3drs876658695
GWAS Ctlgrs876658695
Max Magnitude0
ClinVar
Risk rs876658695(ATTG;ATTG)
Alt rs876658695(ATTG;ATTG)
Reference rs876658695(;)
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.23614865_23614868dupCAAT
CLNSRC
CLNACC RCV000219269.1,