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rs587778584

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23630148
GenePALB2
is asnp
is mentioned by
dbSNPrs587778584
ebirs587778584
HLIrs587778584
Exacrs587778584
Varsomers587778584
Maprs587778584
PheGenIrs587778584
hapmaprs587778584
1000 genomesrs587778584
hgdprs587778584
ensemblrs587778584
gopubmedrs587778584
geneviewrs587778584
scholarrs587778584
googlers587778584
pharmgkbrs587778584
gwascentralrs587778584
openSNPrs587778584
23andMers587778584
23andMe allrs587778584
SNP Nexus

SNPshotrs587778584
SNPdbers587778584
MSV3drs587778584
GWAS Ctlgrs587778584
Max Magnitude7
ClinVar
Risk rs587778584(;)
Alt rs587778584(;)
Reference rs587778584(A;A)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN not specified Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23641469delT
CLNSRC
CLNACC RCV000121754.1, RCV000160806.1, RCV000219207.1,