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rs764509489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 7 Fanconi anemia, complementation group N
(C;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23629818
GenePALB2
is asnp
is mentioned by
dbSNPrs764509489
ebirs764509489
HLIrs764509489
Exacrs764509489
Varsomers764509489
Maprs764509489
PheGenIrs764509489
hapmaprs764509489
1000 genomesrs764509489
hgdprs764509489
ensemblrs764509489
gopubmedrs764509489
geneviewrs764509489
scholarrs764509489
googlers764509489
pharmgkbrs764509489
gwascentralrs764509489
openSNPrs764509489
23andMers764509489
23andMe allrs764509489
SNP Nexus

SNPshotrs764509489
SNPdbers764509489
MSV3drs764509489
GWAS Ctlgrs764509489
Max Magnitude7
ClinVar
Risk rs764509489(C;C)
Alt rs764509489(C;C)
Reference rs764509489(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.23641139G>C
CLNSRC
CLNACC RCV000166057.1,