List of variants in gene DTNA reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.1480G>A (p.Asp494Asn)	rs144880521	0.00037
NM_001386795.1(DTNA):c.1330C>T (p.Arg444Trp)	rs199867593	0.00024
NM_001386795.1(DTNA):c.1652G>A (p.Arg551His)	rs142108185	0.00011
NM_001386795.1(DTNA):c.614C>T (p.Thr205Met)	rs201071018	0.00010
NM_001386795.1(DTNA):c.371A>G (p.His124Arg)	rs150147476	0.00009
NM_001386795.1(DTNA):c.2153G>A (p.Arg718His)	rs111587625	0.00004
NM_001386795.1(DTNA):c.1965G>A (p.Met655Ile)	rs749109824	0.00003
NM_001386795.1(DTNA):c.604-13T>G	rs761037945	0.00003
NM_001386795.1(DTNA):c.182C>G (p.Ala61Gly)	rs767620520	0.00002
NM_001386795.1(DTNA):c.2227C>T (p.Arg743Trp)	rs774768713	0.00002
NM_001386795.1(DTNA):c.869C>T (p.Thr290Met)	rs747834756	0.00002
NM_001386795.1(DTNA):c.1030G>A (p.Asp344Asn)	rs374347283	0.00001
NM_001386795.1(DTNA):c.1613A>G (p.Asn538Ser)	rs770486884	0.00001
NM_001386795.1(DTNA):c.2101C>T (p.His701Tyr)	rs772866088	0.00001
NM_001386795.1(DTNA):c.2195C>T (p.Pro732Leu)	rs1456993704	0.00001
NM_001386795.1(DTNA):c.2228G>A (p.Arg743Gln)	rs371303988	0.00001
NM_001386795.1(DTNA):c.476G>A (p.Ser159Asn)	rs147115867	0.00001
NM_001386795.1(DTNA):c.646G>T (p.Asp216Tyr)	rs769662524	0.00001
NM_001386795.1(DTNA):c.784C>T (p.His262Tyr)	rs369043538	0.00001
NM_001386795.1(DTNA):c.944C>G (p.Pro315Arg)	rs138085660	0.00001
NM_001386795.1(DTNA):c.*2579C>T	rs794729008
NM_001386795.1(DTNA):c.*2690T>C	rs1382811716
NM_001386795.1(DTNA):c.1325T>C (p.Met442Thr)	rs1057524416
NM_001386795.1(DTNA):c.1426T>C (p.Ser476Pro)	rs1057518266
NM_001386795.1(DTNA):c.2309G>A (p.Gly770Asp)	rs1057518465
NM_001386795.1(DTNA):c.331C>T (p.Leu111Phe)	rs1555801105

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