rs753775002

This variant is located in the HMGN4 gene.

ClinVar annotation

Uncertain Significance☆☆☆
1 submitter

not specified

View on ClinVar →

About HMGN4

The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]

View all HMGN4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…