DOT1L c.1005+672C>T

Variant ID: 19-2209647-C-T

NM_032482.2(DOT1L):c.1005+672C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Nature Genetics
Nalls, Mike A MA; Pankratz, Nathan N; Lill, Christina M CM; Do, Chuong B CB; Hernandez, Dena G DG; Saad, Mohamad M; DeStefano, Anita L AL; Kara, Eleanna E; Bras, Jose J; Sharma, Manu M; Schulte, Claudia C; Keller, Margaux F MF; Arepalli, Sampath S; Letson, Christopher C; Edsall, Connor C; Stefansson, Hreinn H; Liu, Xinmin X; Pliner, Hannah H; Lee, Joseph H JH; Cheng, Rong R; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; Ikram, M Arfan MA; Ioannidis, John P A JP; Hadjigeorgiou, Georgios M GM; Bis, Joshua C JC; Martinez, Maria M; Perlmutter, Joel S JS; Goate, Alison A; Marder, Karen K; Fiske, Brian B; Sutherland, Margaret M; Xiromerisiou, Georgia G; Myers, Richard H RH; Clark, Lorraine N LN; Stefansson, Kari K; Hardy, John A JA; Heutink, Peter P; Chen, Honglei H; Wood, Nicholas W NW; Houlden, Henry H; Payami, Haydeh H; Brice, Alexis A; Scott, William K WK; Gasser, Thomas T; Bertram, Lars L; Eriksson, Nicholas N; Foroud, Tatiana T; Singleton, Andrew B AB
Publication Date: 2014-09

Variant appearance in text: rs117022814
PubMed Link: 25064009
Variant Present in the following documents:
  • Main text
  • NIHMS610183-supplement-1.pdf
View BVdb publication page