WDR88 c.1080+954G>C

Variant ID: 19-33652356-G-C

NM_173479.3(WDR88):c.1080+954G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Integration of summary data from GWAS and eQTL studies identified novel causal BMD genes with functional predictions.

Bone
Meng, Xiang-He XH; Chen, Xiang-Ding XD; Greenbaum, Jonathan J; Zeng, Qin Q; You, Sheng-Lan SL; Xiao, Hong-Mei HM; Tan, Li-Jun LJ; Deng, Hong-Wen HW
Publication Date: 2018-08

Variant appearance in text: rs11084710
PubMed Link: 29763751
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.

Journal Of Alzheimer'S Disease : Jad
Sherva, Richard R; Baldwin, Clinton T CT; Inzelberg, Rivka R; Vardarajan, Badri B; Cupples, L Adrienne LA; Lunetta, Kathryn K; Bowirrat, Abdalla A; Naj, Adam A; Pericak-Vance, Margaret M; Friedland, Robert P RP; Farrer, Lindsay A LA
Publication Date: 2011

Variant appearance in text: rs11084710
PubMed Link: 21098978
Variant Present in the following documents:
  • Main text
View BVdb publication page