ClinVar Miner

List of variants reported as uncertain significance for autosomal recessive Alport syndrome by Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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NM_000091.4(COL4A3):c.1909G>A (p.Gly637Arg) rs761686437
NM_000091.4(COL4A3):c.765G>A (p.Thr255=) rs869025328
NM_000092.5(COL4A4):c.4333+3A>G rs1455105815

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