ClinVar Miner

List of variants reported as likely benign for Achondrogenesis

Minimum submission review status: Collection method:
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ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_000112.4(SLC26A2):c.*1892dup rs148778566 0.04587
NM_004239.4(TRIP11):c.*387del rs148331500 0.02205
NM_000112.4(SLC26A2):c.*4870dup rs368872246 0.00983
NM_004239.4(TRIP11):c.*1339dup rs35251290

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