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rs587781411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TC) 3 2-4 fold higher risk for breast cancer, depending on family history
(TC;TC) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23603512
GenePALB2
is asnp
is mentioned by
dbSNPrs587781411
ebirs587781411
HLIrs587781411
Exacrs587781411
Varsomers587781411
Maprs587781411
PheGenIrs587781411
hapmaprs587781411
1000 genomesrs587781411
hgdprs587781411
ensemblrs587781411
gopubmedrs587781411
geneviewrs587781411
scholarrs587781411
googlers587781411
pharmgkbrs587781411
gwascentralrs587781411
openSNPrs587781411
23andMers587781411
23andMe allrs587781411
SNP Nexus

SNPshotrs587781411
SNPdbers587781411
MSV3drs587781411
GWAS Ctlgrs587781411
Max Magnitude7
ClinVar
Risk rs587781411(;)
Alt rs587781411(;)
Reference rs587781411(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23614833_23614834delGA
CLNSRC
CLNACC RCV000129272.2, RCV000133490.1, RCV000211073.2,