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rs587776415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 significantly increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23630080
GenePALB2
is asnp
is mentioned by
dbSNPrs587776415
ebirs587776415
HLIrs587776415
Exacrs587776415
Varsomers587776415
Maprs587776415
PheGenIrs587776415
hapmaprs587776415
1000 genomesrs587776415
hgdprs587776415
ensemblrs587776415
gopubmedrs587776415
geneviewrs587776415
scholarrs587776415
googlers587776415
pharmgkbrs587776415
gwascentralrs587776415
openSNPrs587776415
23andMers587776415
23andMe allrs587776415
SNP Nexus

SNPshotrs587776415
SNPdbers587776415
MSV3drs587776415
GWAS Ctlgrs587776415
Max Magnitude7
ClinVar
Risk rs587776415(T;T)
Alt rs587776415(T;T)
Reference rs587776415(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23641401G>A
CLNSRC ClinVar
CLNACC RCV000133477.1,