List of variants in gene DNM2 reported by OMIM

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.1105C>T (p.Arg369Trp)	rs121909090	0.00001
NM_001005361.3(DNM2):c.1072G>A (p.Gly358Arg)	rs267606772
NM_001005361.3(DNM2):c.1102G>A (p.Glu368Lys)	rs121909092
NM_001005361.3(DNM2):c.1106G>A (p.Arg369Gln)	rs121909089
NM_001005361.3(DNM2):c.1135T>G (p.Phe379Val)	rs397514735
NM_001005361.3(DNM2):c.1393C>T (p.Arg465Trp)	rs121909091
NM_001005361.3(DNM2):c.1609G>T (p.Gly537Cys)	rs121909093
NM_001005361.3(DNM2):c.1664_1671+1del	rs1568314339
NM_001005361.3(DNM2):c.1681AAG[1] (p.Lys562del)	rs1599620408
NM_001005361.3(DNM2):c.1684A>G (p.Lys562Glu)	rs121909088
NM_001005361.3(DNM2):c.1709T>A (p.Leu570His)	rs121909094
NM_001005361.3(DNM2):c.1856C>G (p.Ser619Trp)	rs121909095
NM_001005361.3(DNM2):c.1856C>T (p.Ser619Leu)	rs121909095

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