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rs1562430

From SNPedia

Orientationminus
Stabilizedminus
Make rs1562430(A;A)
Make rs1562430(A;G)
Make rs1562430(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127375606
GeneLOC101930033
is asnp
is mentioned by
dbSNPrs1562430
ebirs1562430
HLIrs1562430
Exacrs1562430
Varsomers1562430
Maprs1562430
PheGenIrs1562430
hapmaprs1562430
1000 genomesrs1562430
hgdprs1562430
ensemblrs1562430
gopubmedrs1562430
geneviewrs1562430
scholarrs1562430
googlers1562430
pharmgkbrs1562430
gwascentralrs1562430
openSNPrs1562430
23andMers1562430
23andMe allrs1562430
SNP Nexus

SNPshotrs1562430
SNPdbers1562430
MSV3drs1562430
GWAS Ctlgrs1562430
GMAF0.3379
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20453838OA-icon.png]
Trait Breast cancer
Title Genome-wide association study identifies five new breast cancer susceptibility loci
Risk Allele T
P-val 6E-7
Odds Ratio 1.17 [1.10-1.25]
GWAS snp
PMID [PMID 21263130]
Trait
Title Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study
Risk Allele A
P-val 3E-11
Odds Ratio 1.1600 [1.11-1.22]


[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies


[PMID 22275265OA-icon.png] Common genetic variants in the 8q24 region and risk of papillary thyroid cancer


[PMID 22452962OA-icon.png] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study

[PMID 19330030OA-icon.png] A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).


[PMID 26248686] Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy