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rs16940342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0 Considered benign according to ClinVar
(G;G) 0 Considered benign according to ClinVar
ReferenceGRCh38 38.1/141
Chromosome16
Position23633265
GenePALB2
is asnp
is mentioned by
dbSNPrs16940342
ebirs16940342
HLIrs16940342
Exacrs16940342
Varsomers16940342
Maprs16940342
PheGenIrs16940342
hapmaprs16940342
1000 genomesrs16940342
hgdprs16940342
ensemblrs16940342
gopubmedrs16940342
geneviewrs16940342
scholarrs16940342
googlers16940342
pharmgkbrs16940342
gwascentralrs16940342
openSNPrs16940342
23andMers16940342
23andMe allrs16940342
SNP Nexus

SNPshotrs16940342
SNPdbers16940342
MSV3drs16940342
GWAS Ctlgrs16940342
GMAF0.1873
Max Magnitude0
? (A;A) (A;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 rs16940342(G;G)
Alt rs16940342(G;G)
Reference rs16940342(A;A)
Significance Non-pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000016.9:g.23644586A>G
CLNSRC PALB2 database
CLNACC RCV000114488.1,



[PMID 18794107] Association of common PALB2 polymorphisms with breast cancer risk: a case-control study.


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