List of variants in gene combination IFT140, LOC126862260 reported as benign for retinal disorder

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014714.4(IFT140):c.2768+184A>G	rs2745178	0.97367
NM_014714.4(IFT140):c.2919C>T (p.Ala973=)	rs2235640	0.19119
NM_014714.4(IFT140):c.3079G>A (p.Gly1027Arg)	rs137995818	0.00236

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