OCA2 c.1951+11892C>T

Variant ID: 15-28185038-G-A

NM_000275.2(OCA2):c.1951+11892C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Web-based, participant-driven studies yield novel genetic associations for common traits.

Plos Genetics
Eriksson, Nicholas N; Macpherson, J Michael JM; Tung, Joyce Y JY; Hon, Lawrence S LS; Naughton, Brian B; Saxonov, Serge S; Avey, Linda L; Wojcicki, Anne A; Pe'er, Itsik I; Mountain, Joanna J
Publication Date: 2010-06-24

Variant appearance in text: rs2594935
PubMed Link: 20585627
Variant Present in the following documents:
  • pgen.1000993.s007.pdf
View BVdb publication page



Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kim, Soo-Jeong SJ; Brune, Camille W CW; Kistner, Emily O EO; Christian, Susan L SL; Courchesne, Eric H EH; Cox, Nancy J NJ; Cook, Edwin H EH
Publication Date: 2008-10-05

Variant appearance in text: rs2594935
PubMed Link: 18361419
Variant Present in the following documents:
  • Main text
View BVdb publication page



Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.

American Journal Of Human Genetics
Kayser, Manfred M; Liu, Fan F; Janssens, A Cecile J W AC; Rivadeneira, Fernando F; Lao, Oscar O; van Duijn, Kate K; Vermeulen, Mark M; Arp, Pascal P; Jhamai, Mila M MM; van Ijcken, Wilfred F J WF; den Dunnen, Johan T JT; Heath, Simon S; Zelenika, Diana D; Despriet, Dominiek D G DD; Klaver, Caroline C W CC; Vingerling, Johannes R JR; de Jong, Paulus T V M PT; Hofman, Albert A; Aulchenko, Yurii S YS; Uitterlinden, Andre G AG; Oostra, Ben A BA; van Duijn, Cornelia M CM
Publication Date: 2008-02

Variant appearance in text: rs2594935
PubMed Link: 18252221
Variant Present in the following documents:
  • Main text
View BVdb publication page