ClinVar Miner

List of variants in gene SLC26A2 reported as likely benign for Achondrogenesis

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000112.4(SLC26A2):c.*1892dup rs148778566 0.04587
NM_000112.4(SLC26A2):c.*4870dup rs368872246 0.00983

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