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rs587781697

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
Position23635892
GenePALB2
is asnp
is mentioned by
dbSNPrs587781697
ebirs587781697
HLIrs587781697
Exacrs587781697
Varsomers587781697
Maprs587781697
PheGenIrs587781697
hapmaprs587781697
1000 genomesrs587781697
hgdprs587781697
ensemblrs587781697
gopubmedrs587781697
geneviewrs587781697
scholarrs587781697
googlers587781697
pharmgkbrs587781697
gwascentralrs587781697
openSNPrs587781697
23andMers587781697
23andMe allrs587781697
SNP Nexus

SNPshotrs587781697
SNPdbers587781697
MSV3drs587781697
GWAS Ctlgrs587781697
Max Magnitude7
ClinVar
Risk rs587781697(;)
Alt rs587781697(;)
Reference rs587781697(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23647213delT
CLNSRC Inc.
CLNACC RCV000129864.3,