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rs515726073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 7 Fanconi anemia, complementation group N
(C;TT) 3 2-4 fold higher risk for breast cancer, depending on family history
(TT;TT) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23634869
GenePALB2
is asnp
is mentioned by
dbSNPrs515726073
ebirs515726073
HLIrs515726073
Exacrs515726073
Varsomers515726073
Maprs515726073
PheGenIrs515726073
hapmaprs515726073
1000 genomesrs515726073
hgdprs515726073
ensemblrs515726073
gopubmedrs515726073
geneviewrs515726073
scholarrs515726073
googlers515726073
pharmgkbrs515726073
gwascentralrs515726073
openSNPrs515726073
23andMers515726073
23andMe allrs515726073
SNP Nexus

SNPshotrs515726073
SNPdbers515726073
MSV3drs515726073
GWAS Ctlgrs515726073
Max Magnitude7
ClinVar
Risk rs515726073(C;C)
Alt rs515726073(C;C)
Reference rs515726073(TT;TT)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene PALB2
CLNDBN Fanconi anemia, complementation group N
Reversed 0
HGVS NC_000016.9:g.23646190_23646191delTTinsC
CLNSRC PALB2 database
CLNACC RCV000114487.1,