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rs587781890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;GT) 3 2-4 fold higher risk for breast cancer, depending on family history
(GT;GT) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23607946
GenePALB2
is asnp
is mentioned by
dbSNPrs587781890
ebirs587781890
HLIrs587781890
Exacrs587781890
Varsomers587781890
Maprs587781890
PheGenIrs587781890
hapmaprs587781890
1000 genomesrs587781890
hgdprs587781890
ensemblrs587781890
gopubmedrs587781890
geneviewrs587781890
scholarrs587781890
googlers587781890
pharmgkbrs587781890
gwascentralrs587781890
openSNPrs587781890
23andMers587781890
23andMe allrs587781890
SNP Nexus

SNPshotrs587781890
SNPdbers587781890
MSV3drs587781890
GWAS Ctlgrs587781890
Max Magnitude7
ClinVar
Risk rs587781890(;)
Alt rs587781890(;)
Reference rs587781890(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.23619267_23619268delAC
CLNSRC
CLNACC RCV000130222.2,