rs759901156
This variant is located in the LHFPL4 gene.
▶ClinVar annotation
About LHFPL4
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. [provided by RefSeq, Jul 2008]
View all LHFPL4 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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