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rs981782

From SNPedia

Orientationminus
Stabilizedminus
Make rs981782(G;G)
Make rs981782(G;T)
Make rs981782(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position45285616
GeneHCN1
is asnp
is mentioned by
dbSNPrs981782
ebirs981782
HLIrs981782
Exacrs981782
Varsomers981782
Maprs981782
PheGenIrs981782
hapmaprs981782
1000 genomesrs981782
hgdprs981782
ensemblrs981782
gopubmedrs981782
geneviewrs981782
scholarrs981782
googlers981782
pharmgkbrs981782
gwascentralrs981782
openSNPrs981782
23andMers981782
23andMe allrs981782
SNP Nexus

SNPshotrs981782
SNPdbers981782
MSV3drs981782
GWAS Ctlgrs981782
GMAF0.3278
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 17529967OA-icon.png]
Trait Breast cancer
Title Genome-wide association study identifies novel breast cancer susceptibility loci
Risk Allele C
P-val 0.0000090000000000000002
Odds Ratio 1.04 [1.01-1.08]

[PMID 18326623OA-icon.png] Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.

[PMID 18681954OA-icon.png] Breast cancer susceptibility loci and mammographic density.

[PMID 18708391OA-icon.png] Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. radiologic technologists.

[PMID 19232126OA-icon.png] Association between breast cancer susceptibility loci and mammographic density: the Multiethnic Cohort.

[PMID 19304784OA-icon.png] Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.

[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.

[PMID 20605201OA-icon.png] Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study.

[PMID 22045194OA-icon.png] Combined effect of low-penetrant SNPs on breast cancer risk.


GET Evidence
rs981782
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary



[PMID 27863437] Association of multiple genetic variants with breast cancer susceptibility in the Han Chinese population.