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rs875989790

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989790(-;-)
Make rs875989790(-;A)
Make rs875989790(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635968
GenePALB2
is asnp
is mentioned by
dbSNPrs875989790
ebirs875989790
HLIrs875989790
Exacrs875989790
Varsomers875989790
Maprs875989790
PheGenIrs875989790
hapmaprs875989790
1000 genomesrs875989790
hgdprs875989790
ensemblrs875989790
gopubmedrs875989790
geneviewrs875989790
scholarrs875989790
googlers875989790
pharmgkbrs875989790
gwascentralrs875989790
openSNPrs875989790
23andMers875989790
23andMe allrs875989790
SNP Nexus

SNPshotrs875989790
SNPdbers875989790
MSV3drs875989790
GWAS Ctlgrs875989790
Max Magnitude0
ClinVar
Risk rs875989790(A;A)
Alt rs875989790(A;A)
Reference rs875989790(;)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647290dupT
CLNSRC
CLNACC RCV000211071.1,