ClinVar Genomic variation as it relates to human health

This variant is classified as Likely Pathogenic. Evidence in support of pathogenic classification: - An inversion involving the SMARCAL1 and MARCHF4 genes has been identified. The inversion includes the promoter region and exons 1 to 17 (of 18) of the SMARCAL1 gene and the promoter region and part of exon 1 (of 4) of the MARCHF4 gene. The impact on the protein is difficult to predict. Multiple protein outcomes including a fusion or truncation are possible and expected to impact protein function. - Very strong and specific phenotype match for this individual . - Heterozygous variant detected in trans with a second pathogenic heterozygous variant (c.250dupC;p.(Gln84Profs*5)) in a recessive disease. Additional information: - This variant is heterozygous. - The SMARCAL1 gene is associated with autosomal recessive disease. - Variant is absent from gnomAD (SV v2). - This variant has no previous evidence of pathogenicity. - No published segregation evidence has been identified for this variant. - No published functional evidence has been identified for this variant. - No comparable inversions or truncating variants have previous evidence for pathogenicity. - Variant does not affect an established domain, motif, hotspot or informative constraint region. - Loss of function is a known mechanism of disease in the SMARCAL1 gene and is associated with Schimke immunoosseous dysplasia (MIM#242900). There is no known gene-disease association for the MARCHF4 gene. - This variant has been shown to be paternally inherited (by trio analysis).