Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AA) 3 significantly increased risk of breast cancer
(AA;AA) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23623045
GenePALB2
is asnp
is mentioned by
dbSNPrs587776421
ebirs587776421
HLIrs587776421
Exacrs587776421
Varsomers587776421
Maprs587776421
PheGenIrs587776421
hapmaprs587776421
1000 genomesrs587776421
hgdprs587776421
ensemblrs587776421
gopubmedrs587776421
geneviewrs587776421
scholarrs587776421
googlers587776421
pharmgkbrs587776421
gwascentralrs587776421
openSNPrs587776421
23andMers587776421
23andMe allrs587776421
SNP Nexus

SNPshotrs587776421
SNPdbers587776421
MSV3drs587776421
GWAS Ctlgrs587776421
Max Magnitude7
ClinVar
Risk rs587776421(;)
Alt rs587776421(;)
Reference rs587776421(AA;AA)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23634365_23634366delTT
CLNSRC PALB2 database
CLNACC RCV000114575.3, RCV000132234.4, RCV000133483.2,