F3 c.591+87T>C

Variant ID: 1-94998559-A-G

NM_001993.4(F3):c.591+87T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs610277
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population.

Pediatric Research
Gimenez, Lucas G LG; Momany, Allison M AM; Poletta, Fernando A FA; Krupitzki, Hugo B HB; Gili, Juan A JA; Busch, Tamara D TD; Saleme, Cesar C; Cosentino, Viviana R VR; Pawluk, Mariela S MS; CampaƱa, Hebe H; Gadow, Enrique C EC; Murray, Jeffrey C JC; Lopez-Camelo, Jorge S JS
Publication Date: 2017-09

Variant appearance in text: rs610277
PubMed Link: 28426651
Variant Present in the following documents:
  • Main text
  • nihms868340.pdf
View BVdb publication page