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rs515726065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;T) 3 significantly increased risk of breast cancer
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23635232
GenePALB2
is asnp
is mentioned by
dbSNPrs515726065
ebirs515726065
HLIrs515726065
Exacrs515726065
Varsomers515726065
Maprs515726065
PheGenIrs515726065
hapmaprs515726065
1000 genomesrs515726065
hgdprs515726065
ensemblrs515726065
gopubmedrs515726065
geneviewrs515726065
scholarrs515726065
googlers515726065
pharmgkbrs515726065
gwascentralrs515726065
openSNPrs515726065
23andMers515726065
23andMe allrs515726065
SNP Nexus

SNPshotrs515726065
SNPdbers515726065
MSV3drs515726065
GWAS Ctlgrs515726065
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726065(;)
Alt rs515726065(;)
Reference rs515726065(T;T)
Significance Pathogenic
Disease Familial cancer of breast Pancreatic cancer 3
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Pancreatic cancer 3
Reversed 0
HGVS NC_000016.9:g.23646553delT
CLNSRC PALB2 database
CLNACC RCV000114467.1, RCV000114468.1,