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rs587782446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635288
GenePALB2
is asnp
is mentioned by
dbSNPrs587782446
ebirs587782446
HLIrs587782446
Exacrs587782446
Varsomers587782446
Maprs587782446
PheGenIrs587782446
hapmaprs587782446
1000 genomesrs587782446
hgdprs587782446
ensemblrs587782446
gopubmedrs587782446
geneviewrs587782446
scholarrs587782446
googlers587782446
pharmgkbrs587782446
gwascentralrs587782446
openSNPrs587782446
23andMers587782446
23andMe allrs587782446
SNP Nexus

SNPshotrs587782446
SNPdbers587782446
MSV3drs587782446
GWAS Ctlgrs587782446
Max Magnitude7
ClinVar
Risk rs587782446(T;T)
Alt rs587782446(T;T)
Reference rs587782446(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646609G>A
CLNSRC
CLNACC RCV000131515.2,