GC c.59-5326A>C

Variant ID: 4-72640443-T-G

NM_000583.3(GC):c.59-5326A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations.

Bioinformatics (Oxford, England)
Cao, Shaolong S; Qin, Huaizhen H; Gossmann, Alexej A; Deng, Hong-Wen HW; Wang, Yu-Ping YP
Publication Date: 2016-02-01

Variant appearance in text: rs1491717
PubMed Link: 26458888
Variant Present in the following documents:
  • Main text
View BVdb publication page