rs981782

Orientation

minus

Stabilized

minus

Make rs981782(G;G)

Make rs981782(G;T)

Make rs981782(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

45285616

Gene

HCN1

is a	snp
is	mentioned by
dbSNP	rs981782
dbSNP (classic)	rs981782
ClinGen	rs981782
ebi	rs981782
HLI	rs981782
Exac	rs981782
Gnomad	rs981782
Varsome	rs981782
LitVar	rs981782
Map	rs981782
PheGenI	rs981782
Biobank	rs981782
1000 genomes	rs981782
hgdp	rs981782
ensembl	rs981782
geneview	rs981782
scholar	rs981782
google	rs981782
pharmgkb	rs981782
gwascentral	rs981782
openSNP	rs981782
23andMe	rs981782
SNPshot	rs981782
SNPdbe	rs981782
MSV3d	rs981782
GWAS Ctlg	rs981782

GMAF

0.3278

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

GWAS snp
PMID	[PMID 17529967 ]
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 18326623 ] Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.

[PMID 18681954 ] Breast cancer susceptibility loci and mammographic density.

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

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

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

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

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

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

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