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rs587782680

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
Position23630102
GenePALB2
is asnp
is mentioned by
dbSNPrs587782680
ebirs587782680
HLIrs587782680
Exacrs587782680
Varsomers587782680
Maprs587782680
PheGenIrs587782680
hapmaprs587782680
1000 genomesrs587782680
hgdprs587782680
ensemblrs587782680
gopubmedrs587782680
geneviewrs587782680
scholarrs587782680
googlers587782680
pharmgkbrs587782680
gwascentralrs587782680
openSNPrs587782680
23andMers587782680
23andMe allrs587782680
SNP Nexus

SNPshotrs587782680
SNPdbers587782680
MSV3drs587782680
GWAS Ctlgrs587782680
Max Magnitude7
ClinVar
Risk rs587782680(;)
Alt rs587782680(;)
Reference rs587782680(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.23641423delG
CLNSRC
CLNACC RCV000132106.3,