GENETIC ENCYCLOPEDIA
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NC_000015.10:g.(?_43638998)_(43639062_?)del AND multiple conditions

Significance: Pathogenic
ClinVar: RCV000826136

Variant: NC_000015.10:g.(?_43638998)_(43639062_?)del

Type: Variant
Allele: NC_000015.10:g.(?_43638998)_(43639062_?)del 654985
Gene:
Type: Deletion
Location: Chr15: 43931196 - 43931260 - assembly GRCh37
References: ClinVar: 38

Conditions

Disease: Rare genetic deafness
Disease: Deafness-infertility syndrome