ClinVar Miner

List of variants studied for autosomal dominant nonsyndromic deafness 13 by Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_080679.2(COL11A2):c.97G>A (p.Asp33Asn)

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