DMRT1 c.539-17494G>T
Variant ID: 9-876418-G-T
NM_021951.2(DMRT1):c.539-17494G>T
This variant was identified in 4 publications
Variant-Specific Resource Links:
Publications:
MAGPEL: an autoMated pipeline for inferring vAriant-driven Gene PanEls from the full-length biomedical literature.
Scientific Reports
Saberian, Nafiseh N; Shafi, Adib A; Peyvandipour, Azam A; Draghici, Sorin S
Publication Date: 2020-07-23
Variant appearance in text: rs11790408
Variant Present in the following documents:
- 41598_2020_68649_MOESM2_ESM.xlsx, sheet 2
Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability.
Elife
Välimäki, Niko N; Kuisma, Heli H; Pasanen, Annukka A; Heikinheimo, Oskari O; Sjöberg, Jari J; Bützow, Ralf R; Sarvilinna, Nanna N; Heinonen, Hanna-Riikka HR; Tolvanen, Jaana J; Bramante, Simona S; Tanskanen, Tomas T; Auvinen, Juha J; Uimari, Outi O; Alkodsi, Amjad A; Lehtonen, Rainer R; Kaasinen, Eevi E; Palin, Kimmo K; Aaltonen, Lauri A LA
Publication Date: 2018-09-18
Variant appearance in text: rs11790408
Variant Present in the following documents:
- Main text
- elife-37110.pdf
An assessment of the portability of ancestry informative markers between human populations.
Bmc Medical Genomics
Myles, Sean S; Stoneking, Mark M; Timpson, Nic N
Publication Date: 2009-07-20
Variant appearance in text: rs11790408
Variant Present in the following documents:
- Main text
- 1755-8794-2-45.pdf
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature
,
Publication Date: 2007-06-07
Variant appearance in text: rs11790408
Variant Present in the following documents: