Have questions? Visit https://www.reddit.com/r/SNPedia

rs515726086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23629764
GenePALB2
is asnp
is mentioned by
dbSNPrs515726086
ebirs515726086
HLIrs515726086
Exacrs515726086
Varsomers515726086
Maprs515726086
PheGenIrs515726086
hapmaprs515726086
1000 genomesrs515726086
hgdprs515726086
ensemblrs515726086
gopubmedrs515726086
geneviewrs515726086
scholarrs515726086
googlers515726086
pharmgkbrs515726086
gwascentralrs515726086
openSNPrs515726086
23andMers515726086
23andMe allrs515726086
SNP Nexus

SNPshotrs515726086
SNPdbers515726086
MSV3drs515726086
GWAS Ctlgrs515726086
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726086(;)
Alt rs515726086(;)
Reference rs515726086(T;T)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000016.10:g.23629764delT
CLNSRC PALB2 database
CLNACC RCV000114525.1,