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rs875989791

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989791(-;-)
Make rs875989791(-;A)
Make rs875989791(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635852
GenePALB2
is asnp
is mentioned by
dbSNPrs875989791
ebirs875989791
HLIrs875989791
Exacrs875989791
Varsomers875989791
Maprs875989791
PheGenIrs875989791
hapmaprs875989791
1000 genomesrs875989791
hgdprs875989791
ensemblrs875989791
gopubmedrs875989791
geneviewrs875989791
scholarrs875989791
googlers875989791
pharmgkbrs875989791
gwascentralrs875989791
openSNPrs875989791
23andMers875989791
23andMe allrs875989791
SNP Nexus

SNPshotrs875989791
SNPdbers875989791
MSV3drs875989791
GWAS Ctlgrs875989791
Max Magnitude0
ClinVar
Risk rs875989791(A;A)
Alt rs875989791(A;A)
Reference rs875989791(;)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647174dupT
CLNSRC
CLNACC RCV000211082.1,