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

rs587780210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 2-4 fold higher risk for breast cancer, depending on family history
(C;C) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23630034
GenePALB2
is asnp
is mentioned by
dbSNPrs587780210
ebirs587780210
HLIrs587780210
Exacrs587780210
Varsomers587780210
Maprs587780210
PheGenIrs587780210
hapmaprs587780210
1000 genomesrs587780210
hgdprs587780210
ensemblrs587780210
gopubmedrs587780210
geneviewrs587780210
scholarrs587780210
googlers587780210
pharmgkbrs587780210
gwascentralrs587780210
openSNPrs587780210
23andMers587780210
23andMe allrs587780210
SNP Nexus

SNPshotrs587780210
SNPdbers587780210
MSV3drs587780210
GWAS Ctlgrs587780210
Max Magnitude7
ClinVar
Risk rs587780210(;)
Alt rs587780210(;)
Reference rs587780210(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23641355delG
CLNSRC
CLNACC RCV000116079.2, RCV000216701.1,