GENETIC ENCYCLOPEDIA
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NC_000015.9:g.43890409_43939642del49234 AND Deafness-infertility syndrome

Significance: Pathogenic
ClinVar: RCV000735212

Variant: NC_000015.9:g.43890409_43939642del49234

Type: Variant
Allele: NC_000015.9:g.43890409_43939642del49234 589819
Gene:
Type: Deletion
Location: Chr15: 43890409 - 43939642 - assembly GRCh37

Condition

Disease: Deafness-infertility syndrome