Variants in gene DNM2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.190G>A (p.Val64Ile)	rs144250390	0.00243
NM_001005361.3(DNM2):c.2179C>T (p.His727Tyr)	rs142963320	0.00024
NM_001005361.3(DNM2):c.958G>A (p.Asp320Asn)	rs150613209	0.00023
NM_001005361.3(DNM2):c.2592C>T (p.Ala864=)	rs373161548	0.00014
NM_001005361.3(DNM2):c.1384A>G (p.Thr462Ala)	rs201575500	0.00011
NM_001005361.3(DNM2):c.316G>A (p.Asp106Asn)	rs375151459	0.00011
NM_001005361.3(DNM2):c.2201A>G (p.Asn734Ser)	rs577767034	0.00006
NM_001005361.3(DNM2):c.890G>A (p.Arg297His)	rs763894364	0.00003
NM_001005361.3(DNM2):c.1196+710G>A	rs140208362	0.00002

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