ClinVar Miner

List of variants in gene MED13L reported by GenomeConnect - Brain Gene Registry

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_015335.5(MED13L):c.3469C>T (p.Gln1157Ter)	rs1555245108
NM_015335.5(MED13L):c.3765del (p.Cys1256fs)	rs147976828
NM_015335.5(MED13L):c.5365-1G>A	rs1876893450

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