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rs876660147

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660147(-;-)
Make rs876660147(-;A)
Make rs876660147(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23624082
GenePALB2
is asnp
is mentioned by
dbSNPrs876660147
ebirs876660147
HLIrs876660147
Exacrs876660147
Varsomers876660147
Maprs876660147
PheGenIrs876660147
hapmaprs876660147
1000 genomesrs876660147
hgdprs876660147
ensemblrs876660147
gopubmedrs876660147
geneviewrs876660147
scholarrs876660147
googlers876660147
pharmgkbrs876660147
gwascentralrs876660147
openSNPrs876660147
23andMers876660147
23andMe allrs876660147
SNP Nexus

SNPshotrs876660147
SNPdbers876660147
MSV3drs876660147
GWAS Ctlgrs876660147
Max Magnitude0
ClinVar
Risk rs876660147(A;A)
Alt rs876660147(A;A)
Reference rs876660147(;)
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.23635404dupT
CLNSRC
CLNACC RCV000223425.1,