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rs875989792

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989792(-;-)
Make rs875989792(-;CAACAAGT)
Make rs875989792(CAACAAGT;CAACAAGT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23622998
GenePALB2
is asnp
is mentioned by
dbSNPrs875989792
ebirs875989792
HLIrs875989792
Exacrs875989792
Varsomers875989792
Maprs875989792
PheGenIrs875989792
hapmaprs875989792
1000 genomesrs875989792
hgdprs875989792
ensemblrs875989792
gopubmedrs875989792
geneviewrs875989792
scholarrs875989792
googlers875989792
pharmgkbrs875989792
gwascentralrs875989792
openSNPrs875989792
23andMers875989792
23andMe allrs875989792
SNP Nexus

SNPshotrs875989792
SNPdbers875989792
MSV3drs875989792
GWAS Ctlgrs875989792
Max Magnitude0
ClinVar
Risk rs875989792(CAACAAGT;CAACAAGT)
Alt rs875989792(CAACAAGT;CAACAAGT)
Reference rs875989792(;)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23634319_23634320insACTTGTTG
CLNSRC
CLNACC RCV000211065.1,