ClinVar Miner

List of variants reported as likely pathogenic for congenital limb malformation by Institute for Genomic Medicine, Nationwide Children's Hospital

Included ClinVar conditions (336):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001003800.2(BICD2):c.1636_1638del (p.Asn546del) rs1064795760

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