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rs587776410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AAGAA) 3 significantly increased risk of breast cancer
(AAGAA;AAGAA) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23635505
GenePALB2
is asnp
is mentioned by
dbSNPrs587776410
ebirs587776410
HLIrs587776410
Exacrs587776410
Varsomers587776410
Maprs587776410
PheGenIrs587776410
hapmaprs587776410
1000 genomesrs587776410
hgdprs587776410
ensemblrs587776410
gopubmedrs587776410
geneviewrs587776410
scholarrs587776410
googlers587776410
pharmgkbrs587776410
gwascentralrs587776410
openSNPrs587776410
23andMers587776410
23andMe allrs587776410
SNP Nexus

SNPshotrs587776410
SNPdbers587776410
MSV3drs587776410
GWAS Ctlgrs587776410
Max Magnitude7
ClinVar
Risk rs587776410(;)
Alt rs587776410(;)
Reference rs587776410(AAGAA;AAGAA)
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.23646826_23646830delTTCTT
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000130093.2, RCV000133471.1, RCV000205410.1,