rs2167270
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0.79x reduced risk for colon cancer | |
(A;G) | 0 | normal |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 128241296 |
Gene | LEP |
is a | snp |
is | mentioned by |
dbSNP | rs2167270 |
dbSNP (classic) | rs2167270 |
ClinGen | rs2167270 |
ebi | rs2167270 |
HLI | rs2167270 |
Exac | rs2167270 |
Gnomad | rs2167270 |
Varsome | rs2167270 |
LitVar | rs2167270 |
Map | rs2167270 |
PheGenI | rs2167270 |
Biobank | rs2167270 |
1000 genomes | rs2167270 |
hgdp | rs2167270 |
ensembl | rs2167270 |
geneview | rs2167270 |
scholar | rs2167270 |
rs2167270 | |
pharmgkb | rs2167270 |
gwascentral | rs2167270 |
openSNP | rs2167270 |
23andMe | rs2167270 |
SNPshot | rs2167270 |
SNPdbe | rs2167270 |
MSV3d | rs2167270 |
GWAS Ctlg | rs2167270 |
GMAF | 0.3503 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs2167270 is a SNP in the leptin LEP gene.
In a study of ~1,500 colon cancer patients, the rs2167270(A;A) genotype was underrepresented, leading to an odds ratio of 0.79 (CI: 0.64-0.98).[PMID 18059035]
[PMID 20140086] Genetic Variation at Selected SNPs in the Leptin Gene and Association of Alleles with Markers of Kidney Disease in a Xhosa Population of South Africa
[PMID 21512510] The Effect of Ponderal Index at Birth on the Relationships Between Common LEP and LEPR Polymorphisms and Adiposity in Adolescents
[PMID 22666399] Tumor Necrosis Factor-α Induced Protein 8 Polymorphism and Risk of Non-Hodgkin's Lymphoma in a Chinese Population: A Case-Control Study
[PMID 15197684] Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study.
[PMID 19035456] Adipokine genes and prostate cancer risk.
[PMID 19204185] Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study.
[PMID 19593725] Association of maternally inherited GNAS alleles with African-American male birth weight.
[PMID 21385539] Lack of association between LEP rs2167270 (19 G>A) polymorphism and disease susceptibility and cardiovascular disease in patients with rheumatoid arthritis.
[PMID 23840460] Lymphotoxin Alpha (LTA) Polymorphism Is Associated with Prognosis of Non-Hodgkin's Lymphoma in a Chinese Population
[PMID 22537818] Polymorphisms in adiposity-related genes are associated with age at menarche and menopause in breast cancer patients and healthy women.
[PMID 22975643] Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance training.
[PMID 24845032] Association of LEP A19G polymorphism with cancer risk: a systematic review and pooled analysis
[PMID 25810718] Polymorphism in LEP and LEPR May Modify Leptin Levels and Represent Risk Factors for Thyroid Cancer
[PMID 26167411] Genetic variants in leptin: Determinants of obesity and leptin levels in South Indian population
ClinVar | |
---|---|
Risk | Rs2167270(A;A) |
Alt | Rs2167270(A;A) |
Reference | Rs2167270(G;G) |
Significance | Probable-non-pathogenic |
Disease | Leptin deficiency or dysfunction Monogenic Non-Syndromic Obesity |
Variation | info |
Gene | LEP |
CLNDBN | Leptin deficiency or dysfunction Monogenic Non-Syndromic Obesity |
Reversed | 0 |
HGVS | NC_000007.13:g.127881349G>A |
CLNSRC | |
CLNACC | RCV000329981.1, RCV000375354.1, |
[PMID 31038568] Adipokine gene variability and plasma levels in patients with chronic periodontitis -a case-control study.
[PMID 32004678] Associations of maternal diet and placenta leptin methylation.
[PMID 32774722] Investigation of Leptin and its receptor (LEPR) for single nucleotide polymorphisms in colorectal cancer: a case-control study involving 2,306 subjects.