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rs515726075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/141
Chromosome16
Position23630207
GenePALB2
is asnp
is mentioned by
dbSNPrs515726075
ebirs515726075
HLIrs515726075
Exacrs515726075
Varsomers515726075
Maprs515726075
PheGenIrs515726075
hapmaprs515726075
1000 genomesrs515726075
hgdprs515726075
ensemblrs515726075
gopubmedrs515726075
geneviewrs515726075
scholarrs515726075
googlers515726075
pharmgkbrs515726075
gwascentralrs515726075
openSNPrs515726075
23andMers515726075
23andMe allrs515726075
SNP Nexus

SNPshotrs515726075
SNPdbers515726075
MSV3drs515726075
GWAS Ctlgrs515726075
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726075(T;T)
Alt rs515726075(T;T)
Reference rs515726075(;)
Significance Other
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000016.9:g.23641528dupT
CLNSRC PALB2 database
CLNACC RCV000114502.2,