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

rs587776411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 significantly increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23635438
GenePALB2
is asnp
is mentioned by
dbSNPrs587776411
ebirs587776411
HLIrs587776411
Exacrs587776411
Varsomers587776411
Maprs587776411
PheGenIrs587776411
hapmaprs587776411
1000 genomesrs587776411
hgdprs587776411
ensemblrs587776411
gopubmedrs587776411
geneviewrs587776411
scholarrs587776411
googlers587776411
pharmgkbrs587776411
gwascentralrs587776411
openSNPrs587776411
23andMers587776411
23andMe allrs587776411
SNP Nexus

SNPshotrs587776411
SNPdbers587776411
MSV3drs587776411
GWAS Ctlgrs587776411
Max Magnitude7
ClinVar
Risk rs587776411(T;T)
Alt rs587776411(T;T)
Reference rs587776411(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23646759G>A
CLNSRC ClinVar
CLNACC RCV000133472.1,