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rs515726104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23621427
GenePALB2
is asnp
is mentioned by
dbSNPrs515726104
ebirs515726104
HLIrs515726104
Exacrs515726104
Varsomers515726104
Maprs515726104
PheGenIrs515726104
hapmaprs515726104
1000 genomesrs515726104
hgdprs515726104
ensemblrs515726104
gopubmedrs515726104
geneviewrs515726104
scholarrs515726104
googlers515726104
pharmgkbrs515726104
gwascentralrs515726104
openSNPrs515726104
23andMers515726104
23andMe allrs515726104
SNP Nexus

SNPshotrs515726104
SNPdbers515726104
MSV3drs515726104
GWAS Ctlgrs515726104
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2
ClinVar
Risk rs515726104(;)
Alt rs515726104(;)
Reference rs515726104(A;A)
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.23632748delA
CLNSRC PALB2 database
CLNACC RCV000114587.1, RCV000129785.2,