Publications:

Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations.

Genes

Stanke, Frauke F; Becker, Tim T; Ismer, Haide Susanne HS; Dunsche, Inga I; Hedtfeld, Silke S; Kontsendorn, Julia J; Dittrich, Anna-Maria AM; Tümmler, Burkhard B

Publication Date: 2021-09-29

Variant appearance in text: rs13333685

PubMed Link: 34680949

Variant Present in the following documents:

• genes-12-01554.pdf

View BVdb publication page