Standard
Adiponectin levels
PEPD · rs4805885
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What each result means
C/C
Published research associates this genotype with typical/baseline likelihood of Adiponectin levels — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2012, PMID:22479202)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Adiponectin levels. (GWAS Catalog, PLoS Genet 2012, PMID:22479202)
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Adiponectin levels compared to the general population. (GWAS Catalog, PLoS Genet 2012, PMID:22479202)
Source
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Dastani Z,
Hivert MF,
Timpson N,
Perry JR,
Yuan X,
Scott RA,
Henneman P,
Heid IM,
Kizer JR,
Lyytikäinen LP,
Fuchsberger C,
Tanaka T
and 548 more — show all
Morris AP,
Small K,
Isaacs A,
Beekman M,
Coassin S,
Lohman K,
Qi L,
Kanoni S,
Pankow JS,
Uh HW,
Wu Y,
Bidulescu A,
Rasmussen-Torvik LJ,
Greenwood CM,
Ladouceur M,
Grimsby J,
Manning AK,
Liu CT,
Kooner J,
Mooser VE,
Vollenweider P,
Kapur KA,
Chambers J,
Wareham NJ,
Langenberg C,
Frants R,
Willems-Vandijk K,
Oostra BA,
Willems SM,
Lamina C,
Winkler TW,
Psaty BM,
Tracy RP,
Brody J,
Chen I,
Viikari J,
Kähönen M,
Pramstaller PP,
Evans DM,
St Pourcain B,
Sattar N,
Wood AR,
Bandinelli S,
Carlson OD,
Egan JM,
Böhringer S,
van Heemst D,
Kedenko L,
Kristiansson K,
Nuotio ML,
Loo BM,
Harris T,
Garcia M,
Kanaya A,
Haun M,
Klopp N,
Wichmann HE,
Deloukas P,
Katsareli E,
Couper DJ,
Duncan BB,
Kloppenburg M,
Adair LS,
Borja JB,
Wilson JG,
Musani S,
Guo X,
Johnson T,
Semple R,
Teslovich TM,
Allison MA,
Redline S,
Buxbaum SG,
Mohlke KL,
Meulenbelt I,
Ballantyne CM,
Dedoussis GV,
Hu FB,
Liu Y,
Paulweber B,
Spector TD,
Slagboom PE,
Ferrucci L,
Jula A,
Perola M,
Raitakari O,
Florez JC,
Salomaa V,
Eriksson JG,
Frayling TM,
Hicks AA,
Lehtimäki T,
Smith GD,
Siscovick DS,
Kronenberg F,
van Duijn C,
Loos RJ,
Waterworth DM,
Meigs JB,
Dupuis J,
Richards JB,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Hofmann OM,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Kong A,
Kraft P,
Kuusisto J,
Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
Rayner NW,
Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Morris AD,
Palmer CN,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Pedersen O,
Barroso I,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Mägi R,
Randall J,
Elliott P,
Rybin D,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Lajunen T,
Doney A,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Mahley R,
Mangino M,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Orrù M,
Pakyz R,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sigurðsson G,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Hu FB 1st,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Penninx BW,
Boomsma DI,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Peltonen L,
Mooser V,
Sladek R,
Musunuru K,
Smith AV,
Edmondson AC,
Stylianou IM,
Koseki M,
Pirruccello JP,
Chasman DI,
Johansen CT,
Fouchier SW,
Peloso GM,
Barbalic M,
Ricketts SL,
Bis JC,
Feitosa MF,
Orho-Melander M,
Melander O,
Li X,
Li M,
Cho YS,
Go MJ,
Kim YJ,
Lee JY,
Park T,
Kim K,
Sim X,
Ong RT,
Croteau-Chonka DC,
Lange LA,
Smith JD,
Ziegler A,
Zhang W,
Zee RY,
Whitfield JB,
Thompson JR,
Surakka I,
Spector TD,
Smit JH,
Sinisalo J,
Scott J,
Saharinen J,
Sabatti C,
Rose LM,
Roberts R,
Rieder M,
Parker AN,
Pare G,
O'Donnell CJ,
Nieminen MS,
Nickerson DA,
Montgomery GW,
McArdle W,
Masson D,
Martin NG,
Marroni F,
Lucas G,
Luben R,
Lokki ML,
Lettre G,
Launer LJ,
Lakatta EG,
Laaksonen R,
Kyvik KO,
König IR,
Khaw KT,
Kaplan LM,
Johansson Å,
Janssens AC,
Igl W,
Hovingh GK,
Hengstenberg C,
Havulinna AS,
Hastie ND,
Harris TB,
Haritunians T,
Hall AS,
Groop LC,
Gonzalez E,
Freimer NB,
Erdmann J,
Ejebe KG,
Döring A,
Dominiczak AF,
Demissie S,
Deloukas P,
de Faire U,
Crawford G,
Chen YD,
Caulfield MJ,
Boekholdt SM,
Assimes TL,
Quertermous T,
Seielstad M,
Wong TY,
Tai ES,
Feranil AB,
Kuzawa CW,
Taylor HA Jr,
Gabriel SB,
Holm H,
Gudnason V,
Krauss RM,
Ordovas JM,
Munroe PB,
Kooner JS,
Tall AR,
Hegele RA,
Kastelein JJ,
Schadt EE,
Strachan DP,
Reilly MP,
Samani NJ,
Schunkert H,
Cupples LA,
Sandhu MS,
Ridker PM,
Rader DJ,
Kathiresan S
PLoS genetics · 2012 · PMID 22479202 · open access
Questions about rs4805885
What is rs4805885?
rs4805885 is a single position in the genome, in or near the PEPD gene. Published research associates it with adiponectin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4805885 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs4805885 come from?
GWAS Catalog, PLoS Genet 2012, PMID:22479202. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants