KITLG c.16-15827C>G

Variant ID: 12-88955469-G-C

NM_000899.4(KITLG):c.16-15827C>G

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Polygenic basis and biomedical consequences of telomere length variation.

Nature Genetics
Codd, Veryan V; Wang, Qingning Q; Allara, Elias E; Musicha, Crispin C; Kaptoge, Stephen S; Stoma, Svetlana S; Jiang, Tao T; Hamby, Stephen E SE; Braund, Peter S PS; Bountziouka, Vasiliki V; Budgeon, Charley A CA; Denniff, Matthew M; Swinfield, Chloe C; Papakonstantinou, Manolo M; Sheth, Shilpi S; Nanus, Dominika E DE; Warner, Sophie C SC; Wang, Minxian M; Khera, Amit V AV; Eales, James J; Ouwehand, Willem H WH; Thompson, John R JR; Di Angelantonio, Emanuele E; Wood, Angela M AM; Butterworth, Adam S AS; Danesh, John N JN; Nelson, Christopher P CP; Samani, Nilesh J NJ
Publication Date: 2021-10

Variant appearance in text: rs1907702
PubMed Link: 34611362
Variant Present in the following documents:
  • 41588_2021_944_MOESM3_ESM.pdf
View BVdb publication page



Polygenic basis and biomedical consequences of telomere length variation.

Nature Genetics
Codd, Veryan V; Wang, Qingning Q; Allara, Elias E; Musicha, Crispin C; Kaptoge, Stephen S; Stoma, Svetlana S; Jiang, Tao T; Hamby, Stephen E SE; Braund, Peter S PS; Bountziouka, Vasiliki V; Budgeon, Charley A CA; Denniff, Matthew M; Swinfield, Chloe C; Papakonstantinou, Manolo M; Sheth, Shilpi S; Nanus, Dominika E DE; Warner, Sophie C SC; Wang, Minxian M; Khera, Amit V AV; Eales, James J; Ouwehand, Willem H WH; Thompson, John R JR; Di Angelantonio, Emanuele E; Wood, Angela M AM; Butterworth, Adam S AS; Danesh, John N JN; Nelson, Christopher P CP; Samani, Nilesh J NJ
Publication Date: 2021-10

Variant appearance in text: rs1907702
PubMed Link: 34611362
Variant Present in the following documents:
  • 41588_2021_944_MOESM3_ESM.pdf
View BVdb publication page



Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.

Nature Communications
Duffy, David L DL; Zhu, Gu G; Li, Xin X; Sanna, Marianna M; Iles, Mark M MM; Jacobs, Leonie C LC; Evans, David M DM; Yazar, Seyhan S; Beesley, Jonathan J; Law, Matthew H MH; Kraft, Peter P; Visconti, Alessia A; Taylor, John C JC; Liu, Fan F; Wright, Margaret J MJ; Henders, Anjali K AK; Bowdler, Lisa L; Glass, Dan D; Ikram, M Arfan MA; Uitterlinden, André G AG; Madden, Pamela A PA; Heath, Andrew C AC; Nelson, Elliot C EC; Green, Adele C AC; Chanock, Stephen S; Barrett, Jennifer H JH; Brown, Matthew A MA; Hayward, Nicholas K NK; MacGregor, Stuart S; Sturm, Richard A RA; Hewitt, Alex W AW; , ; Kayser, Manfred M; Hunter, David J DJ; Newton Bishop, Julia A JA; Spector, Timothy D TD; Montgomery, Grant W GW; Mackey, David A DA; Smith, George Davey GD; Nijsten, Tamar E TE; Bishop, D Timothy DT; Bataille, Veronique V; Falchi, Mario M; Han, Jiali J; Martin, Nicholas G NG
Publication Date: 2018-11-14

Variant appearance in text: rs1907702
PubMed Link: 30429480
Variant Present in the following documents:
  • 41467_2018_6649_MOESM1_ESM.pdf
View BVdb publication page



Identifying the favored mutation in a positive selective sweep.

Nature Methods
Akbari, Ali A; Vitti, Joseph J JJ; Iranmehr, Arya A; Bakhtiari, Mehrdad M; Sabeti, Pardis C PC; Mirarab, Siavash S; Bafna, Vineet V
Publication Date: 2018-04

Variant appearance in text: rs1907702
PubMed Link: 29457793
Variant Present in the following documents:
  • NIHMS937763-supplement-3.pdf
View BVdb publication page



Ethnic characterization of a population of children exposed to high doses of arsenic via drinking water and a possible correlation with metabolic processes.

International Journal Of Molecular Epidemiology And Genetics
Bobillo, Cecilia C; Navoni, Julio A JA; Olmos, Valentina V; Merini, Luciano J LJ; Villaamil Lepori, Edda E; Corach, Daniel D
Publication Date: 2014

Variant appearance in text: rs1907702
PubMed Link: 24596592
Variant Present in the following documents:
  • Main text
View BVdb publication page



Contrasting signals of positive selection in genes involved in human skin-color variation from tests based on SNP scans and resequencing.

Investigative Genetics
de Gruijter, Johanna Maria JM; Lao, Oscar O; Vermeulen, Mark M; Xue, Yali Y; Woodwark, Cara C; Gillson, Christopher J CJ; Coffey, Alison J AJ; Ayub, Qasim Q; Mehdi, S Qasim SQ; Kayser, Manfred M; Tyler-Smith, Chris C
Publication Date: 2011-12-01

Variant appearance in text: rs1907702
PubMed Link: 22133426
Variant Present in the following documents:
  • Main text
  • 2041-2223-2-24.pdf
View BVdb publication page



Evaluating self-declared ancestry of U.S. Americans with autosomal, Y-chromosomal and mitochondrial DNA.

Human Mutation
Lao, Oscar O; Vallone, Peter M PM; Coble, Michael D MD; Diegoli, Toni M TM; van Oven, Mannis M; van der Gaag, Kristiaan J KJ; Pijpe, Jeroen J; de Knijff, Peter P; Kayser, Manfred M
Publication Date: 2010-12

Variant appearance in text: rs1907702
PubMed Link: 20886636
Variant Present in the following documents:
  • Main text
  • humu0031-E1875.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: rs1907702
PubMed Link: 20042077
Variant Present in the following documents:
  • Main text
  • 1471-2156-10-88.pdf
View BVdb publication page