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rs587782531

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(GT;TA) 3 2-4 fold higher risk for breast cancer, depending on family history
(TA;TA) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635884
GenePALB2
is asnp
is mentioned by
dbSNPrs587782531
ebirs587782531
HLIrs587782531
Exacrs587782531
Varsomers587782531
Maprs587782531
PheGenIrs587782531
hapmaprs587782531
1000 genomesrs587782531
hgdprs587782531
ensemblrs587782531
gopubmedrs587782531
geneviewrs587782531
scholarrs587782531
googlers587782531
pharmgkbrs587782531
gwascentralrs587782531
openSNPrs587782531
23andMers587782531
23andMe allrs587782531
SNP Nexus

SNPshotrs587782531
SNPdbers587782531
MSV3drs587782531
GWAS Ctlgrs587782531
Max Magnitude7
ClinVar
Risk rs587782531(TA;TA)
Alt rs587782531(TA;TA)
Reference rs587782531(GT;GT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23647205_23647206delACinsTA
CLNSRC
CLNACC RCV000131730.2,