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rs515726067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 2-4 fold higher risk for breast cancer, depending on family history
(C;C) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23635229
GenePALB2
is asnp
is mentioned by
dbSNPrs515726067
ebirs515726067
HLIrs515726067
Exacrs515726067
Varsomers515726067
Maprs515726067
PheGenIrs515726067
hapmaprs515726067
1000 genomesrs515726067
hgdprs515726067
ensemblrs515726067
gopubmedrs515726067
geneviewrs515726067
scholarrs515726067
googlers515726067
pharmgkbrs515726067
gwascentralrs515726067
openSNPrs515726067
23andMers515726067
23andMe allrs515726067
SNP Nexus

SNPshotrs515726067
SNPdbers515726067
MSV3drs515726067
GWAS Ctlgrs515726067
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726067(;)
Alt rs515726067(;)
Reference rs515726067(C;C)
Significance Pathogenic
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.23646550delC
CLNSRC PALB2 database
CLNACC RCV000114470.4, RCV000129522.4, RCV000212789.2,