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rs876658348

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658348(-;-)
Make rs876658348(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629684
GenePALB2
is asnp
is mentioned by
dbSNPrs876658348
ebirs876658348
HLIrs876658348
Exacrs876658348
Varsomers876658348
Maprs876658348
PheGenIrs876658348
hapmaprs876658348
1000 genomesrs876658348
hgdprs876658348
ensemblrs876658348
gopubmedrs876658348
geneviewrs876658348
scholarrs876658348
googlers876658348
pharmgkbrs876658348
gwascentralrs876658348
openSNPrs876658348
23andMers876658348
23andMe allrs876658348
SNP Nexus

SNPshotrs876658348
SNPdbers876658348
MSV3drs876658348
GWAS Ctlgrs876658348
Max Magnitude0
ClinVar
Risk rs876658348(;)
Alt rs876658348(;)
Reference rs876658348(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.23641005delA
CLNSRC
CLNACC RCV000217072.1,