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rs515726117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 significantly increased risk of breast cancer
(C;C) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23603658
GenePALB2
is asnp
is mentioned by
dbSNPrs515726117
ebirs515726117
HLIrs515726117
Exacrs515726117
Varsomers515726117
Maprs515726117
PheGenIrs515726117
hapmaprs515726117
1000 genomesrs515726117
hgdprs515726117
ensemblrs515726117
gopubmedrs515726117
geneviewrs515726117
scholarrs515726117
googlers515726117
pharmgkbrs515726117
gwascentralrs515726117
openSNPrs515726117
23andMers515726117
23andMe allrs515726117
SNP Nexus

SNPshotrs515726117
SNPdbers515726117
MSV3drs515726117
GWAS Ctlgrs515726117
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2
ClinVar
Risk
Alt
Reference Rs515726117(C;C)
Significance Other
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000016.9:g.23614979delC
CLNSRC PALB2 database
CLNACC RCV000114624.6, RCV000130740.3, RCV000235614.2,