rs10103544

This is a intron variant variant in the RNF19A gene.

GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

level of sperm-associated antigen 1 in blood

Allele C
OR 0.40
p 2.0e-14
N 47,745
Large GWAS
European

About RNF19A

This gene encodes a member of the ring between ring fingers (RBR) protein family, and the encoded protein contains two RING-finger motifs and an in between RING fingers motif. This protein is an E3 ubiquitin ligase that is localized to Lewy bodies, and ubiquitylates synphilin-1, which is an interacting protein of alpha synuclein in neurons. The encoded protein may be involved in amyotrophic lateral sclerosis and Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

View all RNF19A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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