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rs587776406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 significantly increased risk of breast cancer
(A;A) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23637905
GenePALB2
is asnp
is mentioned by
dbSNPrs587776406
ebirs587776406
HLIrs587776406
Exacrs587776406
Varsomers587776406
Maprs587776406
PheGenIrs587776406
hapmaprs587776406
1000 genomesrs587776406
hgdprs587776406
ensemblrs587776406
gopubmedrs587776406
geneviewrs587776406
scholarrs587776406
googlers587776406
pharmgkbrs587776406
gwascentralrs587776406
openSNPrs587776406
23andMers587776406
23andMe allrs587776406
SNP Nexus

SNPshotrs587776406
SNPdbers587776406
MSV3drs587776406
GWAS Ctlgrs587776406
Max Magnitude7
ClinVar
Risk rs587776406(;)
Alt rs587776406(;)
Reference rs587776406(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23649226delT
CLNSRC ClinVar
CLNACC RCV000133474.1,