Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659463

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659463(C;C)
Make rs876659463(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23621357
GenePALB2
is asnp
is mentioned by
dbSNPrs876659463
ebirs876659463
HLIrs876659463
Exacrs876659463
Varsomers876659463
Maprs876659463
PheGenIrs876659463
hapmaprs876659463
1000 genomesrs876659463
hgdprs876659463
ensemblrs876659463
gopubmedrs876659463
geneviewrs876659463
scholarrs876659463
googlers876659463
pharmgkbrs876659463
gwascentralrs876659463
openSNPrs876659463
23andMers876659463
23andMe allrs876659463
SNP Nexus

SNPshotrs876659463
SNPdbers876659463
MSV3drs876659463
GWAS Ctlgrs876659463
Max Magnitude0
ClinVar
Risk rs876659463(C;C)
Alt rs876659463(C;C)
Reference rs876659463(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23632678C>G
CLNSRC
CLNACC RCV000214215.1, RCV000231026.1,