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rs587776424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;CTTA) 3 significantly increased risk of breast cancer
(ACTT;ACTT) 0 common in clinvar
Make rs587776424(CTTA;CTTA)
ReferenceGRCh38 38.1/142
Chromosome16
Position23603594
GenePALB2
is asnp
is mentioned by
dbSNPrs587776424
ebirs587776424
HLIrs587776424
Exacrs587776424
Varsomers587776424
Maprs587776424
PheGenIrs587776424
hapmaprs587776424
1000 genomesrs587776424
hgdprs587776424
ensemblrs587776424
gopubmedrs587776424
geneviewrs587776424
scholarrs587776424
googlers587776424
pharmgkbrs587776424
gwascentralrs587776424
openSNPrs587776424
23andMers587776424
23andMe allrs587776424
SNP Nexus

SNPshotrs587776424
SNPdbers587776424
MSV3drs587776424
GWAS Ctlgrs587776424
Max Magnitude7
ClinVar
Risk rs587776424(;)
Alt rs587776424(;)
Reference rs587776424(ACTT;ACTT)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23614912_23614915delAAGT
CLNSRC ClinVar
CLNACC RCV000133486.1, RCV000165289.1,