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rs587780211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AACCTAC) 3 2-4 fold higher risk for breast cancer, depending on family history
(AACCTAC;AACCTAC) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23629758
GenePALB2
is asnp
is mentioned by
dbSNPrs587780211
ebirs587780211
HLIrs587780211
Exacrs587780211
Varsomers587780211
Maprs587780211
PheGenIrs587780211
hapmaprs587780211
1000 genomesrs587780211
hgdprs587780211
ensemblrs587780211
gopubmedrs587780211
geneviewrs587780211
scholarrs587780211
googlers587780211
pharmgkbrs587780211
gwascentralrs587780211
openSNPrs587780211
23andMers587780211
23andMe allrs587780211
SNP Nexus

SNPshotrs587780211
SNPdbers587780211
MSV3drs587780211
GWAS Ctlgrs587780211
Max Magnitude7
ClinVar
Risk rs587780211(;)
Alt rs587780211(;)
Reference rs587780211(AACCTAC;AACCTAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23641079_23641085delGTAGGTT
CLNSRC
CLNACC RCV000116085.2,