ClinVar Miner

List of variants in gene MED23 reported by MutSpliceDB: a database of splice sites variants effects on splicing, NIH

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004830.4(MED23):c.2427-1G>A
NM_004830.4(MED23):c.2779-1G>C
NM_004830.4(MED23):c.3472-1G>T	rs2114591980

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