ClinVar Miner

List of variants reported as likely benign for auditory system disease by Center for Human Genetics, Inc,Center for Human Genetics, Inc

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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NM_001122659.3(EDNRB):c.914G>A (p.Ser305Asn) rs5352
NM_001354604.2(MITF):c.669G>A (p.Met223Ile) rs1032758072
NM_017780.4(CHD7):c.2053_2058dup (p.Ala685_Lys686dup) rs377139749
NM_017780.4(CHD7):c.8740G>A (p.Gly2914Arg) rs187751757
NM_181458.4(PAX3):c.525G>C (p.Lys175Asn) rs116473352

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