ClinVar Miner

List of variants reported as likely pathogenic for Liang-Wang syndrome by Centre of Medical Genetics, University of Antwerp

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001161352.2(KCNMA1):c.1123G>A (p.Gly375Arg) rs1554829003

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