YWHAZ c.295-6137T>G

Variant ID: 8-101943404-A-C

NM_145690.2(YWHAZ):c.295-6137T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset.

Annals Of Clinical And Translational Neurology
Santos, Diana D; Coelho, Teresa T; Alves-Ferreira, Miguel M; Sequeiros, Jorge J; Mendonça, Denisa D; Alonso, Isabel I; Lemos, Carolina C; Sousa, Alda A
Publication Date: 2017-02

Variant appearance in text: rs17365661
PubMed Link: 28168209
Variant Present in the following documents:
  • Main text
  • ACN3-4-98.pdf
View BVdb publication page



Examination of association of genes in the serotonin system to autism.

Neurogenetics
Anderson, B M BM; Schnetz-Boutaud, N C NC; Bartlett, J J; Wotawa, A M AM; Wright, H H HH; Abramson, R K RK; Cuccaro, M L ML; Gilbert, J R JR; Pericak-Vance, M A MA; Haines, J L JL
Publication Date: 2009-07

Variant appearance in text: rs17365661
PubMed Link: 19184136
Variant Present in the following documents:
  • Main text
View BVdb publication page