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rs587776428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;CT) 3 significantly increased risk of breast cancer
(TC;TC) 0 common in clinvar
Make rs587776428(CT;CT)
ReferenceGRCh38 38.1/142
Chromosome16
Position23603515
GenePALB2
is asnp
is mentioned by
dbSNPrs587776428
ebirs587776428
HLIrs587776428
Exacrs587776428
Varsomers587776428
Maprs587776428
PheGenIrs587776428
hapmaprs587776428
1000 genomesrs587776428
hgdprs587776428
ensemblrs587776428
gopubmedrs587776428
geneviewrs587776428
scholarrs587776428
googlers587776428
pharmgkbrs587776428
gwascentralrs587776428
openSNPrs587776428
23andMers587776428
23andMe allrs587776428
SNP Nexus

SNPshotrs587776428
SNPdbers587776428
MSV3drs587776428
GWAS Ctlgrs587776428
Max Magnitude7
ClinVar
Risk rs587776428(;)
Alt rs587776428(;)
Reference rs587776428(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23614833_23614834delGA
CLNSRC ClinVar
CLNACC RCV000129272.2, RCV000133490.1, RCV000211073.2,