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rs447529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 Benign variant
(C;G) 0 benign variant
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23622102
GenePALB2
is asnp
is mentioned by
dbSNPrs447529
ebirs447529
HLIrs447529
Exacrs447529
Varsomers447529
Maprs447529
PheGenIrs447529
hapmaprs447529
1000 genomesrs447529
hgdprs447529
ensemblrs447529
gopubmedrs447529
geneviewrs447529
scholarrs447529
googlers447529
pharmgkbrs447529
gwascentralrs447529
openSNPrs447529
23andMers447529
23andMe allrs447529
SNP Nexus

SNPshotrs447529
SNPdbers447529
MSV3drs447529
GWAS Ctlgrs447529
GMAF0.1455
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 19921424] Five common single nucleotide polymorphisms in the PALB2 gene and susceptibility to breast cancer in eastern Chinese population


ClinVar
Risk rs447529(C;C)
Alt rs447529(C;C)
Reference rs447529(G;G)
Significance Non-pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23633423C>G
CLNSRC PALB2 database
CLNACC RCV000114584.1,



[PMID 26981788] Role of PALB2 Polymorphisms with Regard to Susceptibility to Female Breast Cancer Risk in the Chinese Population.