ClinVar Miner

List of variants in gene MED23 reported as likely benign for Intellectual disability, autosomal recessive 18

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004830.4(MED23):c.1078-6T>G	rs750247163	0.00001
NM_004830.4(MED23):c.3939+5G>A	rs753015353	0.00001

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