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rs876660719

From SNPedia

Orientationminus
Geno Mag Summary
(ATTCACTCAGATTG;ATTCACTCAGATTG) 0 common in clinvar
Make rs876660719(-;-)
Make rs876660719(-;ATTCACTCAGATTG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23636033
GenePALB2
is asnp
is mentioned by
dbSNPrs876660719
ebirs876660719
HLIrs876660719
Exacrs876660719
Varsomers876660719
Maprs876660719
PheGenIrs876660719
hapmaprs876660719
1000 genomesrs876660719
hgdprs876660719
ensemblrs876660719
gopubmedrs876660719
geneviewrs876660719
scholarrs876660719
googlers876660719
pharmgkbrs876660719
gwascentralrs876660719
openSNPrs876660719
23andMers876660719
23andMe allrs876660719
SNP Nexus

SNPshotrs876660719
SNPdbers876660719
MSV3drs876660719
GWAS Ctlgrs876660719
Max Magnitude0
ClinVar
Risk rs876660719(;)
Alt rs876660719(;)
Reference rs876660719(ATTCACTCAGATTG;ATTCACTCAGATTG)
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.23647354_23647367delCAATCTGAGTGAAT
CLNSRC
CLNACC RCV000217069.1,