ClinVar Miner

List of variants reported as uncertain significance for congenital nystagmus by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

Included ClinVar conditions (48):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_012064.4(MIP):c.513del (p.His172fs) rs1868688386

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