List of variants in gene combination DYNC1H1, LOC126862060 reported as likely benign 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.9049-36G>A	rs118014540	0.00080
NM_001376.5(DYNC1H1):c.9171G>A (p.Gln3057=)	rs201041097	0.00023
NM_001376.5(DYNC1H1):c.9093G>A (p.Thr3031=)	rs145208135	0.00019
NM_001376.5(DYNC1H1):c.9324A>G (p.Glu3108=)	rs142338762	0.00011
NM_001376.5(DYNC1H1):c.9402G>A (p.Pro3134=)	rs145095254	0.00006
NM_001376.5(DYNC1H1):c.9049-19G>T	rs369055747	0.00003
NM_001376.5(DYNC1H1):c.9189C>T (p.His3063=)	rs373124911	0.00003
NM_001376.5(DYNC1H1):c.9075G>A (p.Glu3025=)	rs777623931	0.00002
NM_001376.5(DYNC1H1):c.9263+4C>T	rs375319205	0.00002
NM_001376.5(DYNC1H1):c.9210G>A (p.Pro3070=)	rs201817995	0.00001
NM_001376.5(DYNC1H1):c.9249A>G (p.Pro3083=)	rs1555410963	0.00001
NM_001376.5(DYNC1H1):c.9049-5C>T	rs1555410928
NM_001376.5(DYNC1H1):c.9057T>A (p.Gly3019=)	rs778613903
NM_001376.5(DYNC1H1):c.9069A>G (p.Gly3023=)	rs532073330
NM_001376.5(DYNC1H1):c.9402G>T (p.Pro3134=)	rs145095254

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