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rs515726124

From SNPedia

Merged intors515726123
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
dbSNP (classic)rs515726124
ClinGenrs515726124
ebirs515726124
HLIrs515726124
Exacrs515726124
Gnomadrs515726124
Varsomers515726124
LitVarrs515726124
Maprs515726124
PheGenIrs515726124
Biobankrs515726124
1000 genomesrs515726124
hgdprs515726124
ensemblrs515726124
geneviewrs515726124
scholarrs515726124
googlers515726124
pharmgkbrs515726124
gwascentralrs515726124
openSNPrs515726124
23andMers515726124
SNPshotrs515726124
SNPdbers515726124
MSV3drs515726124
GWAS Ctlgrs515726124
StatusMerged into rs515726123
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
Alt
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, RCV000130658.6, RCV000212776.2,