ClinVar Miner

List of variants in gene SMARCC2 reported by Undiagnosed Diseases Network, NIH

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001330288.2(SMARCC2):c.1926+1G>T rs1555221275

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