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rs515726071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23635067
GenePALB2
is asnp
is mentioned by
dbSNPrs515726071
ebirs515726071
HLIrs515726071
Exacrs515726071
Varsomers515726071
Maprs515726071
PheGenIrs515726071
hapmaprs515726071
1000 genomesrs515726071
hgdprs515726071
ensemblrs515726071
gopubmedrs515726071
geneviewrs515726071
scholarrs515726071
googlers515726071
pharmgkbrs515726071
gwascentralrs515726071
openSNPrs515726071
23andMers515726071
23andMe allrs515726071
SNP Nexus

SNPshotrs515726071
SNPdbers515726071
MSV3drs515726071
GWAS Ctlgrs515726071
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726071(;)
Alt rs515726071(;)
Reference rs515726071(G;G)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.23646388delG
CLNSRC PALB2 database
CLNACC RCV000114478.1, RCV000129889.2,