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rs587776422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 significantly increased risk of breast cancer
(C;C) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23621453
GenePALB2
is asnp
is mentioned by
dbSNPrs587776422
ebirs587776422
HLIrs587776422
Exacrs587776422
Varsomers587776422
Maprs587776422
PheGenIrs587776422
hapmaprs587776422
1000 genomesrs587776422
hgdprs587776422
ensemblrs587776422
gopubmedrs587776422
geneviewrs587776422
scholarrs587776422
googlers587776422
pharmgkbrs587776422
gwascentralrs587776422
openSNPrs587776422
23andMers587776422
23andMe allrs587776422
SNP Nexus

SNPshotrs587776422
SNPdbers587776422
MSV3drs587776422
GWAS Ctlgrs587776422
Max Magnitude7
ClinVar
Risk rs587776422(;)
Alt rs587776422(;)
Reference rs587776422(C;C)
Significance Pathogenic
Disease Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23632770delG
CLNSRC PALB2 database
CLNACC RCV000114586.2, RCV000133484.1, RCV000160811.1,