List of variants in gene combination DYNC2I2, LOC126860772 reported as likely pathogenic for Jeune syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_052844.4(DYNC2I2):c.1177G>A (p.Gly393Ser)	rs587777096	0.00001
NM_052844.4(DYNC2I2):c.1060A>G (p.Thr354Ala)	rs1554771066
NM_052844.4(DYNC2I2):c.1103_1104del (p.Glu368fs)	rs759150616
NM_052844.4(DYNC2I2):c.935T>C (p.Phe312Ser)	rs1554771175
NM_052844.4(DYNC2I2):c.981+1G>A

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