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rs876659997

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659997(-;-)
Make rs876659997(-;A)
Make rs876659997(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629828
GenePALB2
is asnp
is mentioned by
dbSNPrs876659997
ebirs876659997
HLIrs876659997
Exacrs876659997
Varsomers876659997
Maprs876659997
PheGenIrs876659997
hapmaprs876659997
1000 genomesrs876659997
hgdprs876659997
ensemblrs876659997
gopubmedrs876659997
geneviewrs876659997
scholarrs876659997
googlers876659997
pharmgkbrs876659997
gwascentralrs876659997
openSNPrs876659997
23andMers876659997
23andMe allrs876659997
SNP Nexus

SNPshotrs876659997
SNPdbers876659997
MSV3drs876659997
GWAS Ctlgrs876659997
Max Magnitude0
ClinVar
Risk rs876659997(A;A)
Alt rs876659997(A;A)
Reference rs876659997(;)
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.23641150dupT
CLNSRC
CLNACC RCV000218689.1, RCV000236131.1,