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rs587781840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23623001
GenePALB2
is asnp
is mentioned by
dbSNPrs587781840
ebirs587781840
HLIrs587781840
Exacrs587781840
Varsomers587781840
Maprs587781840
PheGenIrs587781840
hapmaprs587781840
1000 genomesrs587781840
hgdprs587781840
ensemblrs587781840
gopubmedrs587781840
geneviewrs587781840
scholarrs587781840
googlers587781840
pharmgkbrs587781840
gwascentralrs587781840
openSNPrs587781840
23andMers587781840
23andMe allrs587781840
SNP Nexus

SNPshotrs587781840
SNPdbers587781840
MSV3drs587781840
GWAS Ctlgrs587781840
Max Magnitude7
ClinVar
Risk rs587781840(;)
Alt rs587781840(;)
Reference rs587781840(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23634322delT
CLNSRC
CLNACC RCV000130137.2,