Skip to main page content
Accesskeys

dbSNP Short Genetic Variations

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1801177

Current Build 153

Released July 9, 2019

Organism
Homo sapiens
Position
chr8:19948197 (GRCh38.p12) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.02337 (2934/125568, TOPMED)
A=0.0265 (2088/78700, PAGE_STUDY)
A=0.0195 (612/31376, GnomAD) (+ 5 more)
A=0.018 (88/5008, 1000G)
A=0.006 (27/4480, Estonian)
A=0.020 (79/3854, ALSPAC)
A=0.021 (78/3708, TWINSUK)
A=0.00 (1/600, NorthernSweden)
Clinical Significance
Reported in ClinVar
Gene : Consequence
LPL : Missense Variant
Publications
35 citations
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p12 chr 8 NC_000008.11:g.19948197G>A
GRCh38.p12 chr 8 NC_000008.11:g.19948197G>C
GRCh37.p13 chr 8 NC_000008.10:g.19805708G>A
GRCh37.p13 chr 8 NC_000008.10:g.19805708G>C
LPL RefSeqGene NG_008855.2:g.51481G>A
LPL RefSeqGene NG_008855.2:g.51481G>C
LPL RefSeqGene NG_008855.1:g.14127G>A
LPL RefSeqGene NG_008855.1:g.14127G>C
Gene: LPL, lipoprotein lipase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LPL transcript NM_000237.3:c.106G>A D [GAC] > N [AAC] Coding Sequence Variant
lipoprotein lipase precursor NP_000228.1:p.Asp36Asn D (Asp) > N (Asn) Missense Variant
LPL transcript NM_000237.3:c.106G>C D [GAC] > H [CAC] Coding Sequence Variant
lipoprotein lipase precursor NP_000228.1:p.Asp36His D (Asp) > H (His) Missense Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: A (allele ID: 16591 )
ClinVar Accession Disease Names Clinical Significance
RCV000001617.4 Hyperlipidemia, familial combined, susceptibility to Risk-Factor
RCV000157298.1 Coronary heart disease Risk-Factor
RCV000352575.1 Hyperlipoproteinemia, type I Likely-Benign
RCV000454647.1 not specified Likely-Benign
RCV000733476.1 not provided Other
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 125568 G=0.97663 A=0.02337
The PAGE Study Global Study-wide 78700 G=0.9735 A=0.0265
The PAGE Study AfricanAmerican Sub 32514 G=0.9553 A=0.0447
The PAGE Study Mexican Sub 10810 G=0.9915 A=0.0085
The PAGE Study Asian Sub 8318 G=1.000 A=0.000
The PAGE Study PuertoRican Sub 7918 G=0.973 A=0.027
The PAGE Study NativeHawaiian Sub 4534 G=0.995 A=0.005
The PAGE Study Cuban Sub 4230 G=0.979 A=0.021
The PAGE Study Dominican Sub 3828 G=0.963 A=0.037
The PAGE Study CentralAmerican Sub 2450 G=0.987 A=0.013
The PAGE Study SouthAmerican Sub 1982 G=0.990 A=0.010
The PAGE Study NativeAmerican Sub 1260 G=0.984 A=0.016
The PAGE Study SouthAsian Sub 856 G=0.99 A=0.01
gnomAD - Genomes Global Study-wide 31376 G=0.9805 A=0.0195
gnomAD - Genomes European Sub 18894 G=0.9890 A=0.0110
gnomAD - Genomes African Sub 8698 G=0.956 A=0.044
gnomAD - Genomes East Asian Sub 1560 G=1.000 A=0.000
gnomAD - Genomes Other Sub 1088 G=0.987 A=0.013
gnomAD - Genomes American Sub 846 G=1.00 A=0.00
gnomAD - Genomes Ashkenazi Jewish Sub 290 G=0.99 A=0.01
1000Genomes Global Study-wide 5008 G=0.982 A=0.018
1000Genomes African Sub 1322 G=0.949 A=0.051
1000Genomes East Asian Sub 1008 G=1.000 A=0.000
1000Genomes Europe Sub 1006 G=0.989 A=0.011
1000Genomes South Asian Sub 978 G=1.00 A=0.00
1000Genomes American Sub 694 G=0.99 A=0.01
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.994 A=0.006
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.980 A=0.020
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.979 A=0.021
Northern Sweden ACPOP Study-wide 600 G=1.00 A=0.00
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A C Note
GRCh38.p12 chr 8 NC_000008.11:g.19...

NC_000008.11:g.19948197=

NC_000008.11:g.19...

NC_000008.11:g.19948197G>A

NC_000008.11:g.19...

NC_000008.11:g.19948197G>C

GRCh37.p13 chr 8 NC_000008.10:g.19...

NC_000008.10:g.19805708=

NC_000008.10:g.19...

NC_000008.10:g.19805708G>A

NC_000008.10:g.19...

NC_000008.10:g.19805708G>C

LPL RefSeqGene NG_008855.2:g.51481= NG_008855.2:g.514...

NG_008855.2:g.51481G>A

NG_008855.2:g.514...

NG_008855.2:g.51481G>C

LPL RefSeqGene NG_008855.1:g.14127= NG_008855.1:g.141...

NG_008855.1:g.14127G>A

NG_008855.1:g.141...

NG_008855.1:g.14127G>C

LPL transcript NM_000237.3:c.106= NM_000237.3:c.106G>A NM_000237.3:c.106G>C
LPL transcript NM_000237.2:c.106= NM_000237.2:c.106G>A NM_000237.2:c.106G>C
lipoprotein lipase precursor NP_000228.1:p.Asp36= NP_000228.1:p.Asp...

NP_000228.1:p.Asp36Asn

NP_000228.1:p.Asp...

NP_000228.1:p.Asp36His

Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

72 SubSNP, 12 Frequency, 5 ClinVar submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss69043143 May 17, 2007 (127)
2 AFFY ss74821529 Aug 16, 2007 (128)
3 CORNELL ss86272356 Mar 23, 2008 (129)
4 ILLUMINA ss161103354 Dec 01, 2009 (131)
5 1000GENOMES ss217321410 Jul 14, 2010 (132)
6 1000GENOMES ss217418258 Jul 14, 2010 (132)
7 1000GENOMES ss217418988 Jul 14, 2010 (132)
8 1000GENOMES ss217422373 Jul 14, 2010 (132)
9 1000GENOMES ss223585593 Jul 14, 2010 (132)
10 OMICIA ss244238716 May 27, 2010 (132)
11 OMIM-CURATED-RECORDS ss252841601 Aug 10, 2010 (132)
12 GMI ss285807982 Apr 25, 2013 (138)
13 NHLBI-ESP ss342253764 May 09, 2011 (134)
14 ILLUMINA ss410878493 Sep 17, 2011 (135)
15 ILLUMINA ss479398777 Sep 08, 2015 (146)
16 1000GENOMES ss490960903 May 04, 2012 (137)
17 EXOME_CHIP ss491410884 May 04, 2012 (137)
18 CLINSEQ_SNP ss491921973 May 04, 2012 (137)
19 ILLUMINA ss535516942 Sep 08, 2015 (146)
20 TISHKOFF ss560600070 Apr 25, 2013 (138)
21 ILLUMINA ss780867928 Sep 08, 2015 (146)
22 ILLUMINA ss783552862 Sep 08, 2015 (146)
23 EVA-GONL ss985272545 Aug 21, 2014 (142)
24 JMKIDD_LAB ss1067495940 Aug 21, 2014 (142)
25 JMKIDD_LAB ss1075339945 Aug 21, 2014 (142)
26 1000GENOMES ss1328914875 Aug 21, 2014 (142)
27 HAMMER_LAB ss1397520191 Sep 08, 2015 (146)
28 EVA_GENOME_DK ss1582593722 Apr 01, 2015 (144)
29 EVA_DECODE ss1594862211 Apr 01, 2015 (144)
30 EVA_UK10K_ALSPAC ss1620133566 Apr 01, 2015 (144)
31 EVA_UK10K_TWINSUK ss1663127599 Apr 01, 2015 (144)
32 EVA_EXAC ss1689111337 Apr 01, 2015 (144)
33 EVA_EXAC ss1689111338 Apr 01, 2015 (144)
34 EVA_MGP ss1711194682 Apr 01, 2015 (144)
35 ILLUMINA ss1752723225 Sep 08, 2015 (146)
36 ILLUMINA ss1917826314 Feb 12, 2016 (147)
37 WEILL_CORNELL_DGM ss1928562308 Feb 12, 2016 (147)
38 ILLUMINA ss1946231524 Feb 12, 2016 (147)
39 ILLUMINA ss1959093829 Feb 12, 2016 (147)
40 JJLAB ss2024980514 Sep 14, 2016 (149)
41 ILLUMINA ss2094832978 Dec 20, 2016 (150)
42 ILLUMINA ss2095209240 Dec 20, 2016 (150)
43 HUMAN_LONGEVITY ss2301287427 Dec 20, 2016 (150)
44 TOPMED ss2470945340 Dec 20, 2016 (150)
45 GNOMAD ss2737022053 Nov 08, 2017 (151)
46 GNOMAD ss2748007629 Nov 08, 2017 (151)
47 GNOMAD ss2864092212 Nov 08, 2017 (151)
48 AFFY ss2985433031 Nov 08, 2017 (151)
49 AFFY ss2986076126 Nov 08, 2017 (151)
50 SWEGEN ss3002804347 Nov 08, 2017 (151)
51 ILLUMINA ss3022826017 Nov 08, 2017 (151)
52 TOPMED ss3555881190 Nov 08, 2017 (151)
53 TOPMED ss3555881191 Nov 08, 2017 (151)
54 ILLUMINA ss3630013605 Oct 12, 2018 (152)
55 ILLUMINA ss3630013606 Oct 12, 2018 (152)
56 ILLUMINA ss3635162163 Oct 12, 2018 (152)
57 ILLUMINA ss3636899247 Oct 12, 2018 (152)
58 ILLUMINA ss3640869453 Oct 12, 2018 (152)
59 ILLUMINA ss3644964698 Oct 12, 2018 (152)
60 OMUKHERJEE_ADBS ss3646373010 Oct 12, 2018 (152)
61 ILLUMINA ss3653366969 Oct 12, 2018 (152)
62 ILLUMINA ss3653366970 Oct 12, 2018 (152)
63 ILLUMINA ss3654194844 Oct 12, 2018 (152)
64 EGCUT_WGS ss3670484364 Jul 13, 2019 (153)
65 EVA_DECODE ss3721555339 Jul 13, 2019 (153)
66 ILLUMINA ss3726520297 Jul 13, 2019 (153)
67 ACPOP ss3735466986 Jul 13, 2019 (153)
68 ILLUMINA ss3744577743 Jul 13, 2019 (153)
69 ILLUMINA ss3745461946 Jul 13, 2019 (153)
70 PAGE_CC ss3771428641 Jul 13, 2019 (153)
71 ILLUMINA ss3772954539 Jul 13, 2019 (153)
72 KHV_HUMAN_GENOMES ss3810881140 Jul 13, 2019 (153)
73 1000Genomes NC_000008.10 - 19805708 Oct 12, 2018 (152)
74 The Avon Longitudinal Study of Parents and Children NC_000008.10 - 19805708 Oct 12, 2018 (152)
75 Genetic variation in the Estonian population NC_000008.10 - 19805708 Oct 12, 2018 (152)
76 ExAC

Submission ignored due to conflicting rows:
Row 9204915 (NC_000008.10:19805707:G:G 119597/121408, NC_000008.10:19805707:G:A 1811/121408)
Row 9204916 (NC_000008.10:19805707:G:G 121405/121408, NC_000008.10:19805707:G:C 3/121408)

- Oct 12, 2018 (152)
77 ExAC

Submission ignored due to conflicting rows:
Row 9204915 (NC_000008.10:19805707:G:G 119597/121408, NC_000008.10:19805707:G:A 1811/121408)
Row 9204916 (NC_000008.10:19805707:G:G 121405/121408, NC_000008.10:19805707:G:C 3/121408)

- Oct 12, 2018 (152)
78 gnomAD - Genomes NC_000008.10 - 19805708 Jul 13, 2019 (153)
79 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 6190395 (NC_000008.10:19805707:G:G 247930/251484, NC_000008.10:19805707:G:A 3554/251484)
Row 6190396 (NC_000008.10:19805707:G:G 251479/251484, NC_000008.10:19805707:G:C 5/251484)

- Jul 13, 2019 (153)
80 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 6190395 (NC_000008.10:19805707:G:G 247930/251484, NC_000008.10:19805707:G:A 3554/251484)
Row 6190396 (NC_000008.10:19805707:G:G 251479/251484, NC_000008.10:19805707:G:C 5/251484)

- Jul 13, 2019 (153)
81 Northern Sweden NC_000008.10 - 19805708 Jul 13, 2019 (153)
82 The PAGE Study NC_000008.11 - 19948197 Jul 13, 2019 (153)
83 TopMed NC_000008.11 - 19948197 Oct 12, 2018 (152)
84 UK 10K study - Twins NC_000008.10 - 19805708 Oct 12, 2018 (152)
85 ClinVar RCV000001617.4 Jul 13, 2019 (153)
86 ClinVar RCV000157298.1 Oct 12, 2018 (152)
87 ClinVar RCV000352575.1 Oct 12, 2018 (152)
88 ClinVar RCV000454647.1 Oct 12, 2018 (152)
89 ClinVar RCV000733476.1 Jul 13, 2019 (153)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs52806281 Sep 21, 2007 (128)
rs386481815 Aug 06, 2014 (136)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss217321410, ss217418258, ss217418988, ss217422373, ss285807982, ss491921973, ss1397520191, ss1594862211 NC_000008.9:19849987:G:A NC_000008.11:19948196:G:A (self)
41009610, 22796943, 16222612, 112010494, 8751851, 22796943, ss223585593, ss342253764, ss479398777, ss490960903, ss491410884, ss535516942, ss560600070, ss780867928, ss783552862, ss985272545, ss1067495940, ss1075339945, ss1328914875, ss1582593722, ss1620133566, ss1663127599, ss1689111337, ss1711194682, ss1752723225, ss1917826314, ss1928562308, ss1946231524, ss1959093829, ss2024980514, ss2094832978, ss2095209240, ss2470945340, ss2737022053, ss2748007629, ss2864092212, ss2985433031, ss2986076126, ss3002804347, ss3022826017, ss3630013605, ss3630013606, ss3635162163, ss3636899247, ss3640869453, ss3644964698, ss3646373010, ss3653366969, ss3653366970, ss3654194844, ss3670484364, ss3735466986, ss3744577743, ss3745461946, ss3772954539 NC_000008.10:19805707:G:A NC_000008.11:19948196:G:A (self)
RCV000001617.4, RCV000157298.1, RCV000352575.1, RCV000454647.1, RCV000733476.1, 650110, 384681040, ss244238716, ss252841601, ss2301287427, ss3555881190, ss3721555339, ss3726520297, ss3771428641, ss3810881140 NC_000008.11:19948196:G:A NC_000008.11:19948196:G:A (self)
ss69043143, ss74821529, ss86272356, ss161103354, ss410878493 NT_167187.1:7663853:G:A NC_000008.11:19948196:G:A (self)
ss1689111338, ss2737022053 NC_000008.10:19805707:G:C NC_000008.11:19948196:G:C (self)
ss3555881191 NC_000008.11:19948196:G:C NC_000008.11:19948196:G:C (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

35 citations for rs1801177
PMID Title Author Year Journal
8199176 The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity. Nevin DN et al. 1994 Arteriosclerosis and thrombosis
8541837 A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia. Reymer PW et al. 1995 Human molecular genetics
8872057 Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia. de Bruin TW et al. 1996 European journal of clinical investigation
10364086 Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart study. Wittrup HH et al. 1999 Arteriosclerosis, thrombosis, and vascular biology
10517255 Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins. Boer JM et al. 1999 Clinical genetics
12535736 Enhanced bridging function and augmented monocyte adhesion by lipoprotein lipase N9: insights into increased risk of coronary artery disease in N9 carriers. Fisher RM et al. 2003 Atherosclerosis
17357073 Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol. Pare G et al. 2007 American journal of human genetics
18513389 New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background. Penco S et al. 2008 BMC bioinformatics
18922999 Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis. Sagoo GS et al. 2008 American journal of epidemiology
19041386 Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. Boes E et al. 2009 Experimental gerontology
19131662 A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients. Wang X et al. 2009 Stroke
19489872 Association of polymorphisms in genes involved in lipoprotein metabolism with plasma concentrations of remnant lipoproteins and HDL subpopulations before and after hormone therapy in postmenopausal women. Lamon-Fava S et al. 2010 Clinical endocrinology
19501493 A composite scoring of genotypes discriminates coronary heart disease risk beyond conventional risk factors in the Boston Puerto Rican Health Study. Junyent M et al. 2010 Nutrition, metabolism, and cardiovascular diseases
19602472 Lipid and endothelium-related genes, ambient particulate matter, and heart rate variability--the VA Normative Aging Study. Ren C et al. 2010 Journal of epidemiology and community health
20406163 Fenofibrate and metabolic syndrome. Kraja AT et al. 2010 Endocrine, metabolic & immune disorders drug targets
20410100 Genetic variation in APOJ, LPL, and TNFRSF10B affects plasma fatty acid distribution in Alaskan Eskimos. Voruganti VS et al. 2010 The American journal of clinical nutrition
20421590 Genetic causes of high and low serum HDL-cholesterol. Weissglas-Volkov D et al. 2010 Journal of lipid research
20429872 Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study. Ariza MJ et al. 2010 BMC medical genetics
20650961 Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar. Smith AJ et al. 2010 Human molecular genetics
21146168 LPL polymorphism (D9N) predicts cardiovascular disease risk directly and through interaction with CETP polymorphism (TaqIB) in women with high HDL cholesterol and CRP. Corsetti JP et al. 2011 Atherosclerosis
22229114 Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids. Carlquist JF et al. 2011 Journal of clinical & experimental cardiology
22236405 LPL gene variants affect apoC-III response to combination therapy of statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia. Brautbar A et al. 2012 Journal of lipid research
22239554 Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia. Surendran RP et al. 2012 Journal of internal medicine
24033266 A systematic approach to assessing the clinical significance of genetic variants. Duzkale H et al. 2013 Clinical genetics
24319689 The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolism. de Almeida ER et al. 2013 BioMed research international
25626708 Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levels. Pirim D et al. 2015 European journal of human genetics
26786614 Interaction of lipoprotein lipase polymorphisms with body mass index and birth weight to modulate lipid profiles in children and adolescents: the CASPIAN-III Study. Askari G et al. 2016 Sao Paulo medical journal = Revista paulista de medicina
26971241 Influence of Genetic Risk Factors on Coronary Heart Disease Occurrence in Afro-Caribbeans. Larifla L et al. 2016 The Canadian journal of cardiology
27227539 The Contribution of GWAS Loci in Familial Dyslipidemias. Ripatti P et al. 2016 PLoS genetics
27716211 A 19-SNP coronary heart disease gene score profile in subjects with type 2 diabetes: the coronary heart disease risk in type 2 diabetes (CoRDia study) study baseline characteristics. Beaney KE et al. 2016 Cardiovascular diabetology
28143480 Common variants in the genes of triglyceride and HDL-C metabolism lack association with coronary artery disease in the Pakistani subjects. Shahid SU et al. 2017 Lipids in health and disease
28167353 Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants. Shahid SU et al. 2017 Atherosclerosis
29175215 PdPt nanoparticles anchored on the N-G with the integration of PANI nanohybrids as novel redox probe and catalyst for the detection of rs1801177. Wu J et al. 2018 Biosensors & bioelectronics
30026888 Prediction of dyslipidemia using gene mutations, family history of diseases and anthropometric indicators in children and adolescents: The CASPIAN-III study. Marateb HR et al. 2018 Computational and structural biotechnology journal
30805016 Logic Regression Analysis of Gene Polymorphisms and HDL Levels in a Nationally Representative Sample of Iranian Adolescents: The CASPIAN-III Study. Moghadasi M et al. 2017 International journal of endocrinology and metabolism

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post246+3cda961