List of variants in gene combination DNM2, MIR6793 reported by Invitae

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.2059-5C>T	rs377150057	0.00078
NM_001005361.3(DNM2):c.2059-20T>G	rs765782246	0.00012
NM_001005361.3(DNM2):c.2059-4G>A	rs755212019	0.00001
NM_001005361.3(DNM2):c.2059-13C>A
NM_001005361.3(DNM2):c.2059-8G>A	rs1217572149

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