ClinVar Miner

List of variants in gene ADNP2, ATP9B, CTDP1, HSBP1L1, KCNG2, NFATC1, PARD6G, RBFA, SLC66A2, TXNL4A studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
Multiple alleles
NC_000018.9:g.76841645_78077248del1235604
NC_000018.9:g.76854774_78077248del1222475

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