List of variants in gene DYNC1H1 reported as likely benign by Athena Diagnostics Inc

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.13181C>T (p.Thr4394Met)	rs149300055	0.00042
NM_001376.5(DYNC1H1):c.10522C>A (p.Leu3508Ile)	rs149496322	0.00019
NM_001376.5(DYNC1H1):c.12072G>A (p.Pro4024=)	rs537688769	0.00003
NM_001376.5(DYNC1H1):c.7896G>A (p.Leu2632=)	rs17512467	0.00003
NM_001376.5(DYNC1H1):c.13422C>T (p.Thr4474=)	rs765088845	0.00001
NM_001376.5(DYNC1H1):c.13749C>T (p.Thr4583=)	rs746971715	0.00001
NM_001376.5(DYNC1H1):c.2346C>T (p.Ile782=)	rs375810066

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