OCA2 c.646+1412A>G

Variant ID: 15-28266235-T-C

NM_000275.2(OCA2):c.646+1412A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A global view of the OCA2-HERC2 region and pigmentation.

Human Genetics
Donnelly, Michael P MP; Paschou, Peristera P; Grigorenko, Elena E; Gurwitz, David D; Barta, Csaba C; Lu, Ru-Band RB; Zhukova, Olga V OV; Kim, Jong-Jin JJ; Siniscalco, Marcello M; New, Maria M; Li, Hui H; Kajuna, Sylvester L B SL; Manolopoulos, Vangelis G VG; Speed, William C WC; Pakstis, Andrew J AJ; Kidd, Judith R JR; Kidd, Kenneth K KK
Publication Date: 2012-05

Variant appearance in text: rs746861
PubMed Link: 22065085
Variant Present in the following documents:
  • Main text
  • 439_2011_Article_1110.pdf
View BVdb publication page



Genetic determinants of hair and eye colours in the Scottish and Danish populations.

Bmc Genetics
Mengel-From, Jonas J; Wong, Terence H TH; Morling, Niels N; Rees, Jonathan L JL; Jackson, Ian J IJ
Publication Date: 2009-12-30

Variant appearance in text: rs746861
PubMed Link: 20042077
Variant Present in the following documents:
  • Main text
  • 1471-2156-10-88.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: rs746861
PubMed Link: 18361419
Variant Present in the following documents:
  • Main text
View BVdb publication page