Note I have hypertriglycerides & Test Beyond the Range of Tests[edit]
Chromosome One[edit]
- Rs1167998-Risk Allele: C Ch1
- Rs10889353-Risk Allele:C Ch1
Chromosome Two[edit]
- Rs6754295-Risk Allele:C Ch2
Chromosome Three[edit]
- ' rs1470579 3 187011774 AA-Risk Allele C [AA Normal]'
http://www.snpedia.com/index.php/Rs1470579
Chromosome Four[edit]
- Rs10516430-'Risk' Allele:A Ch4 [Decreased]
- Rs346923-'Risk' Allele:A Ch4 [Decreased]
Chromosome Seven[edit]
- Rs2240466-Risk Allele:G Ch7
- Rs7903146-Risk Allele:T Ch10
- PMID [PMID 17463246]
- Title Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
- http://www.snpedia.com/index.php/Rs7903146
Chromosome Eleven[edit]
- ' "rs651821","11","116167789","TT"=Most Common/Major Allele '
[PMID 19732897] Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese
- ' "rs2266788","11","116165896","AA"=TT ' Most Common/Major Allele
[PMID 19732897] Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese
http://www.snpedia.com/index.php/Rs2266788
- ' "rs2075291","11","116166602","CC" '
- Rs2075291(C;C)=normal[Most Common] Ch11
- I both Chinese and non-Chinese Asians, the A allele (leading to the cysteine) is associated with higher risk for hypertriglyceridemia.
- http://www.snpedia.com/index.php/Rs2075291
- Rs2072560-Most Common Allele=C http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=2072560
- [PMID 20395964] Different effects of apolipoprotein A5 SNPs and haplotypes on triglyceride concentration in three ethnic origins
- http://www.snpedia.com/index.php/Rs2072560
- Rs10892151-Risk Allele:A Ch11
- Rs12272004 CC Most Common Ch11
Chromosome Twelve[edit]
- Rs1042615-Risk Allele:CC Ch12 Orientation minus
- "rs1042615","12","61830476","AA"=TT
- [PMID 19056558] rs1042615(T) had
- lower concentrations of triglycerides than did CC carriers (1.36 +/- 0.77 compared with 1.42 +/- 0.89 mmol/L; P = **0.014), especially in nondiabetic subjects (P = 0.001) higher fasting blood glucose (5.20 +/- 1.44 mmol/L compared with 5.12 +/- 1.22 mmol/L; P = 0.036) a tendency toward an increased prevalence of diabetes (odds ratio: 1.22; 95% CI: 0.99, 1.51; P = 0.067)
- "rs2241220","12","108159412","CC"
- Most Common Allele
- http://www.snpedia.com/index.php/Rs1468271
Chromosome 14[edit]
- "rs4986938","14","63769569","TC"=AG GG Most Common Ch14 [Except In Utah]
Chromosome 17[edit]
- rs2229416 17 32683979 CC=GG-Orientation minus
- Most Common Allele-Not at Risk
- http://www.snpedia.com/index.php/Rs2229416
Chromosome 19[edit]
- Rs2304130 AA Most Common Ch19
- ' ""rs7412","19","50103919","CC"-Most Common Allele
Chromosome X[edit]
- Rs5982533-'Risk' Allele:G ChX [Decreased]
Mixed Batch for Hypertriglyceridemia[edit]
Mutation skew in genes identified by genome-wide association study of hypertriglyceridemia
- Locus......SNP........CHR..........Minor Allele..OR (95% CI)........P-value.........John Lloyd Scharf's Genotype
- APOA5......rs964184........11.....G...............3.28 (2.61-4.14)...5.4 × 10-24.....CC
- GCKR........rs1260326.......2......T...............1.75 (1.45-2.12)...6.5 × 10-9.......CT
- ANGPTL3..rs10889353.....1......C..............0.73 (0.59-0.89)...0.002...............AC
- NCAN........rs17216525...19......T..............0.71 (0.50-1.00)...0.05.................CC
