rs680
Orientation | minus |
Stabilized | minus |
Make rs680(A;A) |
Make rs680(A;G) |
Make rs680(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2132404 |
Gene | IGF2, INS-IGF2 |
is a | snp |
is | mentioned by |
dbSNP | rs680 |
dbSNP (classic) | rs680 |
ClinGen | rs680 |
ebi | rs680 |
HLI | rs680 |
Exac | rs680 |
Gnomad | rs680 |
Varsome | rs680 |
LitVar | rs680 |
Map | rs680 |
PheGenI | rs680 |
Biobank | rs680 |
1000 genomes | rs680 |
hgdp | rs680 |
ensembl | rs680 |
geneview | rs680 |
scholar | rs680 |
rs680 | |
pharmgkb | rs680 |
gwascentral | rs680 |
openSNP | rs680 |
23andMe | rs680 |
SNPshot | rs680 |
SNPdbe | rs680 |
MSV3d | rs680 |
GWAS Ctlg | rs680 |
GMAF | 0.2851 |
Max Magnitude | 0 |
[PMID 19953105] Dairy intake associates with the IGF rs680 polymorphism to height variation in periadolescent children
[PMID 21824047] Genetic polymorphisms associated with steroids metabolism and insulin action in polycystic ovary syndrome
[PMID 21926269] Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy
[PMID 22347413] Smoking, Green Tea Consumption, Genetic Polymorphisms in the Insulin-Like Growth Factors and Lung Cancer Risk
[PMID 22666415] Prenatal Famine and Genetic Variation Are Independently and Additively Associated with DNA Methylation at Regulatory Loci within IGF2/H19
[PMID 17012269] Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.
[PMID 17289909] IGF-II gene region polymorphisms related to exertional muscle damage.
[PMID 18085551] Haplotype analysis of the IGF2-INS-TH gene cluster in Parkinson's disease.
[PMID 18603647] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 20403199] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
[PMID 20644730] Telomeric NAP1L4 and OSBPL5 of the KCNQ1 cluster, and the DECORIN gene are not imprinted in human trophoblast stem cells.
[PMID 22565227] Genetic variants in IGF-I, IGF-II, IGFBP-3, and adiponectin genes and colon cancer risk in African Americans and Whites.
[PMID 25117571] Circulating IGF1 and IGF2 and SNP genotypes in pregnant and non-pregnant women and men
[PMID 25923461] IGF2, LEPR, POMC, PPARG, and PPARGC1 gene variants are associated with obesity-related risk phenotypes in Brazilian children and adolescents