PKHD1 c.11666-948G>A

Variant ID: 6-51492862-C-T

NM_138694.3(PKHD1):c.11666-948G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank.

Nature Communications
Wuttke, Matthias M; König, Eva E; Katsara, Maria-Alexandra MA; Kirsten, Holger H; Farahani, Saeed Khomeijani SK; Teumer, Alexander A; Li, Yong Y; Lang, Martin M; Göcmen, Burulca B; Pattaro, Cristian C; Günzel, Dorothee D; Köttgen, Anna A; Fuchsberger, Christian C
Publication Date: 2023-03-09

Variant appearance in text: rs12212034
PubMed Link: 36890159
Variant Present in the following documents:
  • Main text
  • 41467_2023_36864_MOESM3_ESM.xlsx, sheet 6
  • 41467_2023_Article_36864.pdf
View BVdb publication page