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rs875989789

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs875989789(-;-)
Make rs875989789(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23636023
GenePALB2
is asnp
is mentioned by
dbSNPrs875989789
ebirs875989789
HLIrs875989789
Exacrs875989789
Varsomers875989789
Maprs875989789
PheGenIrs875989789
hapmaprs875989789
1000 genomesrs875989789
hgdprs875989789
ensemblrs875989789
gopubmedrs875989789
geneviewrs875989789
scholarrs875989789
googlers875989789
pharmgkbrs875989789
gwascentralrs875989789
openSNPrs875989789
23andMers875989789
23andMe allrs875989789
SNP Nexus

SNPshotrs875989789
SNPdbers875989789
MSV3drs875989789
GWAS Ctlgrs875989789
Max Magnitude0
ClinVar
Risk rs875989789(;)
Alt rs875989789(;)
Reference rs875989789(AA;AA)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647344_23647345delTT
CLNSRC
CLNACC RCV000211064.1,