List of variants in gene combination IFT122, LOC126806810 reported as likely benign for bone development disease

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_052989.3(IFT122):c.2060G>A (p.Arg687Gln)	rs61740161	0.07498
NM_052989.3(IFT122):c.2154C>T (p.His718=)	rs116819033	0.01164
NM_052989.3(IFT122):c.2112G>A (p.Gly704=)
NM_052989.3(IFT122):c.2121T>C (p.His707=)	rs763504971
NM_052989.3(IFT122):c.2127C>T (p.Ala709=)
NM_052989.3(IFT122):c.2148T>C (p.Ser716=)	rs2108483305
NM_052989.3(IFT122):c.2163C>T (p.Leu721=)
NM_052989.3(IFT122):c.2181C>T (p.Thr727=)	rs545131069
NM_052989.3(IFT122):c.2208+7T>C

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