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rs587782892

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
Position23629949
GenePALB2
is asnp
is mentioned by
dbSNPrs587782892
ebirs587782892
HLIrs587782892
Exacrs587782892
Varsomers587782892
Maprs587782892
PheGenIrs587782892
hapmaprs587782892
1000 genomesrs587782892
hgdprs587782892
ensemblrs587782892
gopubmedrs587782892
geneviewrs587782892
scholarrs587782892
googlers587782892
pharmgkbrs587782892
gwascentralrs587782892
openSNPrs587782892
23andMers587782892
23andMe allrs587782892
SNP Nexus

SNPshotrs587782892
SNPdbers587782892
MSV3drs587782892
GWAS Ctlgrs587782892
Max Magnitude7
ClinVar
Risk rs587782892(;)
Alt rs587782892(;)
Reference rs587782892(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.23641270delT
CLNSRC
CLNACC RCV000132530.2,