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rs587781560

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
Position23635000
GenePALB2
is asnp
is mentioned by
dbSNPrs587781560
ebirs587781560
HLIrs587781560
Exacrs587781560
Varsomers587781560
Maprs587781560
PheGenIrs587781560
hapmaprs587781560
1000 genomesrs587781560
hgdprs587781560
ensemblrs587781560
gopubmedrs587781560
geneviewrs587781560
scholarrs587781560
googlers587781560
pharmgkbrs587781560
gwascentralrs587781560
openSNPrs587781560
23andMers587781560
23andMe allrs587781560
SNP Nexus

SNPshotrs587781560
SNPdbers587781560
MSV3drs587781560
GWAS Ctlgrs587781560
Max Magnitude7
ClinVar
Risk rs587781560(;)
Alt rs587781560(;)
Reference rs587781560(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23646321delT
CLNSRC
CLNACC RCV000129579.2, RCV000196008.1,