RARB c.787-6245G>T

Variant ID: 3-25628749-G-T

NM_000965.3(RARB):c.787-6245G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association study between genetic variants in retinol metabolism pathway genes and prostate cancer risk.

Cancer Medicine
Cao, Dongliang D; Meng, Yixuan Y; Li, Shuwei S; Xin, Junyi J; Ben, Shuai S; Cheng, Yifei Y; Wang, Meilin M; Hua, Lixin L; Cheng, Gong G
Publication Date: 2020-12

Variant appearance in text: rs4681028
PubMed Link: 33068330
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: rs4681028
PubMed Link: 27651465
Variant Present in the following documents:
  • Main text
  • eje-175-633.pdf
View BVdb publication page