Have questions? Visit https://www.reddit.com/r/SNPedia

rs515726124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TC) 3 significantly increased risk of breast cancer
(TC;TC) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23636036
GenePALB2
is asnp
is mentioned by
dbSNPrs515726124
ebirs515726124
HLIrs515726124
Exacrs515726124
Varsomers515726124
Maprs515726124
PheGenIrs515726124
hapmaprs515726124
1000 genomesrs515726124
hgdprs515726124
ensemblrs515726124
gopubmedrs515726124
geneviewrs515726124
scholarrs515726124
googlers515726124
pharmgkbrs515726124
gwascentralrs515726124
openSNPrs515726124
23andMers515726124
23andMe allrs515726124
SNP Nexus

SNPshotrs515726124
SNPdbers515726124
MSV3drs515726124
GWAS Ctlgrs515726124
Max Magnitude7
[PMID 25099575OA-icon.png] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic) and [PMID 20122277OA-icon.png]

ClinVar
Risk rs515726124(;)
Alt rs515726124(;)
Reference rs515726124(TC;TC)
Significance Pathogenic
Disease Familial cancer of breast Pancreatic cancer 3 Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Pancreatic cancer 3 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000016.9:g.23647357_23647358delTC
CLNSRC PALB2 database
CLNACC RCV000114645.5, RCV000114646.1, RCV000130658.5, RCV000212776.1,