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rs876658170

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876658170(-;-)
Make rs876658170(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629857
GenePALB2
is asnp
is mentioned by
dbSNPrs876658170
ebirs876658170
HLIrs876658170
Exacrs876658170
Varsomers876658170
Maprs876658170
PheGenIrs876658170
hapmaprs876658170
1000 genomesrs876658170
hgdprs876658170
ensemblrs876658170
gopubmedrs876658170
geneviewrs876658170
scholarrs876658170
googlers876658170
pharmgkbrs876658170
gwascentralrs876658170
openSNPrs876658170
23andMers876658170
23andMe allrs876658170
SNP Nexus

SNPshotrs876658170
SNPdbers876658170
MSV3drs876658170
GWAS Ctlgrs876658170
Max Magnitude0
ClinVar
Risk rs876658170(;)
Alt rs876658170(;)
Reference rs876658170(TC;TC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000016.9:g.23641178_23641179delGA
CLNSRC
CLNACC RCV000220967.1, RCV000236917.1,