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rs587782081

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635947
GenePALB2
is asnp
is mentioned by
dbSNPrs587782081
ebirs587782081
HLIrs587782081
Exacrs587782081
Varsomers587782081
Maprs587782081
PheGenIrs587782081
hapmaprs587782081
1000 genomesrs587782081
hgdprs587782081
ensemblrs587782081
gopubmedrs587782081
geneviewrs587782081
scholarrs587782081
googlers587782081
pharmgkbrs587782081
gwascentralrs587782081
openSNPrs587782081
23andMers587782081
23andMe allrs587782081
SNP Nexus

SNPshotrs587782081
SNPdbers587782081
MSV3drs587782081
GWAS Ctlgrs587782081
Max Magnitude7
ClinVar
Risk rs587782081(;)
Alt rs587782081(;)
Reference rs587782081(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23647268delA
CLNSRC
CLNACC RCV000130577.2, RCV000235246.1,