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rs515726081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TA) 3 2-4 fold higher risk for breast cancer, depending on family history
(TA;TA) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23630008
GenePALB2
is asnp
is mentioned by
dbSNPrs515726081
ebirs515726081
HLIrs515726081
Exacrs515726081
Varsomers515726081
Maprs515726081
PheGenIrs515726081
hapmaprs515726081
1000 genomesrs515726081
hgdprs515726081
ensemblrs515726081
gopubmedrs515726081
geneviewrs515726081
scholarrs515726081
googlers515726081
pharmgkbrs515726081
gwascentralrs515726081
openSNPrs515726081
23andMers515726081
23andMe allrs515726081
SNP Nexus

SNPshotrs515726081
SNPdbers515726081
MSV3drs515726081
GWAS Ctlgrs515726081
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk rs515726081(;)
Alt rs515726081(;)
Reference rs515726081(TA;TA)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000016.9:g.23641329_23641330delTA
CLNSRC PALB2 database
CLNACC RCV000114513.2,