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rs515726126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/141
Chromosome16
Position23635788
GenePALB2
is asnp
is mentioned by
dbSNPrs515726126
ebirs515726126
HLIrs515726126
Exacrs515726126
Varsomers515726126
Maprs515726126
PheGenIrs515726126
hapmaprs515726126
1000 genomesrs515726126
hgdprs515726126
ensemblrs515726126
gopubmedrs515726126
geneviewrs515726126
scholarrs515726126
googlers515726126
pharmgkbrs515726126
gwascentralrs515726126
openSNPrs515726126
23andMers515726126
23andMe allrs515726126
SNP Nexus

SNPshotrs515726126
SNPdbers515726126
MSV3drs515726126
GWAS Ctlgrs515726126
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726126(A;A)
Alt rs515726126(A;A)
Reference rs515726126(;)
Significance Other
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000016.9:g.23647109dupA
CLNSRC PALB2 database
CLNACC RCV000114661.5, RCV000129208.3, RCV000212780.1,