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rs587782232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635695
GenePALB2
is asnp
is mentioned by
dbSNPrs587782232
ebirs587782232
HLIrs587782232
Exacrs587782232
Varsomers587782232
Maprs587782232
PheGenIrs587782232
hapmaprs587782232
1000 genomesrs587782232
hgdprs587782232
ensemblrs587782232
gopubmedrs587782232
geneviewrs587782232
scholarrs587782232
googlers587782232
pharmgkbrs587782232
gwascentralrs587782232
openSNPrs587782232
23andMers587782232
23andMe allrs587782232
SNP Nexus

SNPshotrs587782232
SNPdbers587782232
MSV3drs587782232
GWAS Ctlgrs587782232
Max Magnitude7
ClinVar
Risk rs587782232(A;A)
Alt rs587782232(A;A)
Reference rs587782232(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23647017dupT
CLNSRC
CLNACC RCV000130929.2,