SOS1 c.87+15384T>G

Variant ID: 2-39332093-A-C

NM_005633.3(SOS1):c.87+15384T>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Data on a genome-wide association study of type 2 diabetes in a Maya population.

Data In Brief
Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP
Publication Date: 2020-02

Variant appearance in text: rs2168043
PubMed Link: 31872004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.

European Journal Of Endocrinology
Stevens, Adam A; Murray, Philip P; Wojcik, Jerome J; Raelson, John J; Koledova, Ekaterina E; Chatelain, Pierre P; Clayton, Peter P; ,
Publication Date: 2016-12

Variant appearance in text: rs2168043
PubMed Link: 27651465
Variant Present in the following documents:
  • Main text
  • eje-175-633.pdf
View BVdb publication page



A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.

European Journal Of Endocrinology
Clayton, P P; Chatelain, P P; Tatò, L L; Yoo, H W HW; Ambler, G R GR; Belgorosky, A A; Quinteiro, S S; Deal, C C; Stevens, A A; Raelson, J J; Croteau, P P; Destenaves, B B; Olivier, C C
Publication Date: 2013-09

Variant appearance in text: rs2168043
PubMed Link: 23761422
Variant Present in the following documents:
  • Main text
  • EJE130069.pdf
View BVdb publication page