SYN2 c.774+1259T>C

Variant ID: 3-12194085-T-C

NM_133625.6(SYN2):c.774+1259T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association of TIMP4 gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China.

Peerj
Wang, Jiaqi J; An, Feimeng F; Cao, Yuju Y; Gao, Hongyan H; Sun, Mingqi M; Ma, Chao C; Wu, Hao H; Zhang, Baoxin B; Liu, Wanlin W; Wang, Jianzhong J
Publication Date: 2019

Variant appearance in text: rs99365
PubMed Link: 30697482
Variant Present in the following documents:
  • Main text
  • peerj-07-6270.pdf
View BVdb publication page



Association of synapsin 2 with schizophrenia in families of Northern European ancestry.

Schizophrenia Research
Saviouk, Viatcheslav V; Moreau, Michael P MP; Tereshchenko, Irina V IV; Brzustowicz, Linda M LM
Publication Date: 2007-11

Variant appearance in text: rs99365
PubMed Link: 17766091
Variant Present in the following documents:
  • Main text
View BVdb publication page