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rs587776408

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
Position23635660
GenePALB2
is asnp
is mentioned by
dbSNPrs587776408
ebirs587776408
HLIrs587776408
Exacrs587776408
Varsomers587776408
Maprs587776408
PheGenIrs587776408
hapmaprs587776408
1000 genomesrs587776408
hgdprs587776408
ensemblrs587776408
gopubmedrs587776408
geneviewrs587776408
scholarrs587776408
googlers587776408
pharmgkbrs587776408
gwascentralrs587776408
openSNPrs587776408
23andMers587776408
23andMe allrs587776408
SNP Nexus

SNPshotrs587776408
SNPdbers587776408
MSV3drs587776408
GWAS Ctlgrs587776408
Max Magnitude7
ClinVar
Risk rs587776408(;)
Alt rs587776408(;)
Reference rs587776408(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23646981delT
CLNSRC ClinVar
CLNACC RCV000133493.1,