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rs515726111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23608013
GenePALB2
is asnp
is mentioned by
dbSNPrs515726111
ClinGenrs515726111
ebirs515726111
HLIrs515726111
Exacrs515726111
Varsomers515726111
Maprs515726111
PheGenIrs515726111
hapmaprs515726111
1000 genomesrs515726111
hgdprs515726111
ensemblrs515726111
gopubmedrs515726111
geneviewrs515726111
scholarrs515726111
googlers515726111
pharmgkbrs515726111
gwascentralrs515726111
openSNPrs515726111
23andMers515726111
23andMe allrs515726111
SNP Nexus

SNPshotrs515726111
SNPdbers515726111
MSV3drs515726111
GWAS Ctlgrs515726111
Max Magnitude7
ClinVar
Risk Rs515726111(G;G)
Alt Rs515726111(G;G)
Reference Rs515726111(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided
Reversed 0
HGVS NC_000016.9:g.23619334C>G
CLNSRC PALB2 database
CLNACC RCV000114605.1, RCV000160851.2,