NR0B2 c.148T>C ;(p.C50R)

Variant ID: 1-27240284-A-G

NM_021969.2(NR0B2):c.148T>C;(p.C50R)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids.

Hepatology Communications
Handelman, Samuel K SK; Puentes, Yindra M YM; Kuppa, Annapurna A; Chen, Yanhua Y; Du, Xiaomeng X; Feitosa, Mary F MF; Palmer, Nicholette D ND; Speliotes, Elizabeth K EK
Publication Date: 2022-11

Variant appearance in text: SHP: C50R
PubMed Link: 36098472
Variant Present in the following documents:
  • Main text
  • HEP4-6-3120-s001.xlsx, sheet 7
  • HEP4-6-3120.pdf
View BVdb publication page